| ID: 132090082 | Neanderthal introgressed variant-containing enhancer experimental_26902 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26250596..26250765) | | |
| ID: 132090081 | Neanderthal introgressed variant-containing enhancer experimental_26866 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26214993..26215162) | | |
| ID: 130007574 | ATAC-STARR-seq lymphoblastoid active region 6122 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26318617..26318666) | | |
| ID: 130007573 | ATAC-STARR-seq lymphoblastoid active region 6121 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26275188..26275237) | | |
| ID: 130007572 | ATAC-STARR-seq lymphoblastoid active region 6120 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26274728..26275167) | | |
| ID: 130007571 | ATAC-STARR-seq lymphoblastoid active region 6119 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26271969..26272188) | | |
| ID: 130007570 | ATAC-STARR-seq lymphoblastoid active region 6118 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26245267..26245446) | | |
| ID: 130007569 | ATAC-STARR-seq lymphoblastoid silent region 4301 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26126449..26126618) | | |
| ID: 130007568 | ATAC-STARR-seq lymphoblastoid silent region 4300 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26114160..26114509) | | |
| ID: 130007567 | ATAC-STARR-seq lymphoblastoid silent region 4299 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26097126..26097195) | | |
| ID: 127823837 | H3K4me1 hESC enhancer GRCh37_chr12:26379181-26379816 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26226248..26226883) | | |
| ID: 127823836 | OCT4-NANOG hESC enhancer GRCh37_chr12:26200376-26200975 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26047443..26048042) | | |
| ID: 126861482 | MED14-independent group 3 enhancer GRCh37_chr12:26398995-26400194 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26246062..26247261) | | |
| ID: 124902901 | uncharacterized LOC124902901 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26009948..26011388, complement) | | |
| ID: 107984482 | uncharacterized LOC107984482 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26322920..26332065, complement) | | |
| ID: 105369705 | uncharacterized LOC105369705 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26252872..26310455) | | |
| ID: 105369704 | uncharacterized LOC105369704 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26273329..26276055, complement) | | |
| ID: 101928554 | ITPR2 and SSPN antisense RNA 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26211156..26271827, complement) | | |
| ID: 79365 | basic helix-loop-helix family member e41 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (26120030..26125037, complement) | BHLHB3, DEC2, FNSS1, SHARP1, hDEC2 | 606200 |
| ID: 11228 | Ras association domain family member 8 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (25958232..26079889) | C12orf2, HOJ1 | 608231 |