ID: 132090144 | Neanderthal introgressed variant-containing enhancer experimental_31139 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95982470..95982639) | | |
ID: 129390536 | MPRA-validated peak1901 silencer [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95838318..95838518) | | |
ID: 128772385 | melanoma risk locus-associated MPRA allelic enhancer 12:96379806 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95985956..95986100) | | |
ID: 128772384 | melanoma risk locus-associated MPRA allelic enhancer 12:96249988 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95856138..95856282) | | |
ID: 128772383 | melanoma risk locus-associated MPRA allelic enhancer 12:96244864 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95851014..95851158) | | |
ID: 128772382 | melanoma risk locus-associated MPRA allelic enhancer 12:96243941 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95850091..95850235) | | |
ID: 127824785 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr12:96364529-96365174 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95970751..95971396) | | |
ID: 127824784 | H3K27ac hESC enhancer GRCh37_chr12:96363883-96364528 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95970105..95970750) | | |
ID: 127824783 | H3K4me1 hESC enhancer GRCh37_chr12:96350642-96351154 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95956864..95957376) | | |
ID: 127824782 | H3K4me1 hESC enhancer GRCh37_chr12:96350128-96350641 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95956350..95956863) | | |
ID: 127824781 | NANOG-H3K4me1 hESC enhancer GRCh37_chr12:96322471-96322972 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95928693..95929194) | | |
ID: 127824780 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:96302056-96302565 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95908278..95908787) | | |
ID: 127824779 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:96301545-96302055 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95907767..95908277) | | |
ID: 127824778 | H3K27ac hESC enhancer GRCh37_chr12:96252439-96253054 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95858661..95859276) | | |
ID: 114803471 | AMDHD1 eExon liver enhancer [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95966152..95966636) | | |
ID: 105369921 | SNRPF divergent transcript [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95795345..95858839, complement) | | |
ID: 105369920 | long intergenic non-protein coding RNA 2410 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95803097..95823314) | | |
ID: 144193 | amidohydrolase domain containing 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95943331..95968720) | HMFT1272 | 620863 |
ID: 120935 | coiled-coil domain containing 38 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95867048..95943233, complement) | | |
ID: 6636 | small nuclear ribonucleoprotein polypeptide F [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95858952..95866140) | SMF, Sm-F, snRNP-F | 603541 |