ID: 132089545 | Neanderthal introgressed variant-containing enhancer experimental_99247 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45221626..45221795) | | |
ID: 129998401 | ATAC-STARR-seq lymphoblastoid active region 25971 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45204213..45204372) | | |
ID: 129998400 | ATAC-STARR-seq lymphoblastoid active region 25970 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45140863..45140932) | | |
ID: 129998399 | ATAC-STARR-seq lymphoblastoid silent region 18164 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45118978..45119077) | | |
ID: 127409058 | H3K4me1 hESC enhancer GRCh37_chr7:45281321-45281820 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45241722..45242221) | | |
ID: 127409057 | H3K4me1 hESC enhancer GRCh37_chr7:45280819-45281320 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45241220..45241721) | | |
ID: 127409056 | H3K4me1 hESC enhancer GRCh37_chr7:45230075-45230721 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45190476..45191122) | | |
ID: 127409055 | H3K4me1 hESC enhancer GRCh37_chr7:45217100-45217600 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45177501..45178001) | | |
ID: 127409054 | H3K4me1 hESC enhancer GRCh37_chr7:45173420-45173920 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45133821..45134321) | | |
ID: 127409053 | H3K4me1 hESC enhancer GRCh37_chr7:45163452-45164277 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45123853..45124678) | | |
ID: 127409052 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:45151068-45151823 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45111396..45112224) | | |
ID: 124901624 | uncharacterized LOC124901624 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45306129..45325102) | | |
ID: 124901623 | uncharacterized LOC124901623 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45201701..45208129) | | |
ID: 107986736 | uncharacterized LOC107986736 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45258035..45260064, complement) | | |
ID: 100419775 | zinc finger protein 519 pseudogene [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45303620..45304362) | | |
ID: 677796 | small nucleolar RNA, H/ACA box 5C [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45104906..45105042, complement) | ACA5c | 611335 |
ID: 677795 | small nucleolar RNA, H/ACA box 5B [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45105968..45106099, complement) | ACA5b | |
ID: 10268 | receptor activity modifying protein 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45157791..45184250) | | 605155 |
ID: 9238 | transforming growth factor beta regulator 4 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (45100100..45111697, complement) | CPR2, FASTKD4 | 611325 |