ID: 130007511 | ATAC-STARR-seq lymphoblastoid active region 6072 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (15882345..15882464) | | |
ID: 130007510 | ATAC-STARR-seq lymphoblastoid active region 6071 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (15881805..15882034) | | |
ID: 129663103 | ReSE screen-validated silencer GRCh37_chr12:16069411-16069624 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (15916477..15916690) | | |
ID: 129390404 | MPRA-validated peak1581 silencer [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (15948582..15948782) | | |
ID: 127823752 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:16535886-16536478 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16382952..16383544) | | |
ID: 127823751 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:16535292-16535885 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16382358..16382951) | | |
ID: 127823750 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:16501529-16502458 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16348595..16349524) | | |
ID: 127823749 | NANOG-H3K27ac hESC enhancer GRCh37_chr12:16499669-16500598 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16346735..16347664) | | |
ID: 127823748 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr12:16064701-16065444 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (15911767..15912510) | | |
ID: 127823747 | H3K27ac hESC enhancer GRCh37_chr12:16063956-16064700 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (15911022..15911766) | | |
ID: 126861469 | BRD4-independent group 4 enhancer GRCh37_chr12:16089367-16090566 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (15936433..15937632) | | |
ID: 124625916 | Sharpr-MPRA regulatory region 9686 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16359895..16360189) | | |
ID: 124625915 | Sharpr-MPRA regulatory region 3277 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16030875..16031169) | | |
ID: 124625914 | Sharpr-MPRA regulatory region 5867 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (15879395..15879689) | | |
ID: 110120934 | VISTA enhancer hs798 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16017656..16018890) | | |
ID: 102724146 | uncharacterized LOC102724146 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (15817069..15882298, complement) | | |
ID: 101928362 | uncharacterized LOC101928362 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16107509..16276525) | | |
ID: 100420503 | egl-9 family hypoxia-inducible factor 3 pseudogene 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (15971818..15972802, complement) | | |
ID: 729025 | solute carrier family 15 member 5 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16188485..16277685, complement) | | 620324 |
ID: 400011 | SPT16 homolog, facilitates chromatin remodeling subunit pseudogene 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (16398875..16402509, complement) | SUPT16HP, bcm670 | |