ID: 127409216 | H3K4me1 hESC enhancer GRCh37_chr7:54612500-54613012 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (54544807..54545319) | | |
ID: 127409215 | H3K4me1 hESC enhancer GRCh37_chr7:54609706-54610206 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (54542013..54542513) | | |
ID: 126860043 | BRD4-independent group 4 enhancer GRCh37_chr7:54582481-54583680 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (54514788..54515987) | | |
ID: 124901829 | small nucleolar RNA U13 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (54359892..54359995) | | |
ID: 124901635 | uncharacterized LOC124901635 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (54576052..54578798, complement) | | |
ID: 106480061 | RNA, U6 small nuclear 1125, pseudogene [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (54621025..54621131) | | |
ID: 285878 | VSTM2A overlapping transcript 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (54556970..54571726) | GS1-18A18.1 | |
ID: 222008 | V-set and transmembrane domain containing 2A [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (54542375..54571067) | VSTM2 | |
ID: 222005 | solute carrier family 25 member 5 pseudogene 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (54419371..54420600) | ANTP1 | |