ID: 132090102 | Neanderthal introgressed variant-containing enhancer experimental_28199 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30921963..30922132) | | |
ID: 130007627 | ATAC-STARR-seq lymphoblastoid active region 6161 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30986095..30986144) | | |
ID: 129663115 | ReSE screen-validated silencer GRCh37_chr12:31181720-31181949 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (31028786..31029015) | | |
ID: 129663114 | ReSE screen-validated silencer GRCh37_chr12:31165500-31165701 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (31012566..31012767) | | |
ID: 127823893 | H3K4me1 hESC enhancer GRCh37_chr12:31256969-31257468 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (31104035..31104534) | | |
ID: 127823892 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:31232984-31233540 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (31080050..31080606) | | |
ID: 127823891 | H3K27ac hESC enhancer GRCh37_chr12:31227509-31228038 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (31074555..31075104) | | |
ID: 127823890 | H3K27ac hESC enhancer GRCh37_chr12:31226445-31226976 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (31073511..31074042) | | |
ID: 127823889 | H3K4me1 hESC enhancer GRCh37_chr12:31141041-31141540 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30988106..30988605) | | |
ID: 127823888 | H3K4me1 hESC enhancer GRCh37_chr12:31140539-31141040 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30987604..30988105) | | |
ID: 127823887 | H3K4me1 hESC enhancer GRCh37_chr12:31134009-31134508 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30981074..30981573) | | |
ID: 127823886 | H3K4me1 hESC enhancer GRCh37_chr12:31133507-31134008 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30980572..30981073) | | |
ID: 127823885 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:31130578-31131412 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30977643..30978477) | | |
ID: 127823884 | H3K4me1 hESC enhancer GRCh37_chr12:31117766-31118266 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30964831..30965331) | | |
ID: 127823883 | H3K4me1 hESC enhancer GRCh37_chr12:31062613-31063113 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30909679..30910179) | | |
ID: 127823882 | H3K4me1 hESC enhancer GRCh37_chr12:31027609-31028110 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30874675..30875176) | | |
ID: 124902911 | uncharacterized LOC124902911 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30918507..30926689, complement) | | |
ID: 124902910 | TSPAN11 antisense RNA 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30978308..31005972, complement) | | |
ID: 124629339 | Sharpr-MPRA regulatory region 7044 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (31066315..31066609) | | |
ID: 111082964 | peptidylprolyl isomerase A pseudogene 44 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30861921..30862179) | | |