ID: 129935732 | ATAC-STARR-seq lymphoblastoid silent region 12398 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227325303..227325592) | | |
ID: 129935731 | ATAC-STARR-seq lymphoblastoid active region 17198 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227325073..227325122) | | |
ID: 129935730 | ATAC-STARR-seq lymphoblastoid silent region 12397 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227164678..227164857) | | |
ID: 129935729 | ATAC-STARR-seq lymphoblastoid active region 17196 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (226970499..226970568) | | |
ID: 129389002 | MPRA-validated peak4069 silencer [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227376920..227377120) | | |
ID: 127275910 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:228185522-228186050 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227320806..227321334) | | |
ID: 127275909 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:228050272-228050810 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227185556..227186094) | | |
ID: 127275908 | H3K4me1 hESC enhancer GRCh37_chr2:228028248-228029149 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227163532..227164457) | | |
ID: 127275907 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:227929821-227930408 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227065105..227065692) | | |
ID: 126806540 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr2:228235290-228236489 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227370574..227371773) | | |
ID: 126806539 | MED14-independent group 3 enhancer GRCh37_chr2:228055439-228056638 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227190723..227191922) | | |
ID: 126806538 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:227859794-227860993 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (226995078..226996277) | | |
ID: 124900533 | small nucleolar RNA SNORA48 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (226968989..226969122, complement) | | |
ID: 112441428 | small cysteine and glycine repeat containing 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227387683..227387949, complement) | KRTAP28-1 | |
ID: 100420436 | stress induced phosphoprotein 1 pseudogene 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227335556..227336993) | | |
ID: 654841 | MFF divergent transcript [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227221052..227325164, complement) | | |
ID: 84236 | rhomboid domain containing 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (226800159..226999210) | RHBDL4, RRP4 | 617515 |
ID: 79853 | transmembrane 4 L six family member 20 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227362038..227381647, complement) | PRO994, SLI5, TCCE518 | 615404 |
ID: 56947 | mitochondrial fission factor [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227325251..227357836) | C2orf33, EMPF2, GL004 | 614785 |
ID: 1286 | collagen type IV alpha 4 chain [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (226967360..227164488, complement) | ATS2, BFH, BFH1, CA44 | 120131 |