| ID: 132090851 | Neanderthal introgressed variant-containing enhancer experimental_31344 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98445254..98445423) | | |
| ID: 130008517 | ATAC-STARR-seq lymphoblastoid active region 6842 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98503913..98504212) | | |
| ID: 130008516 | ATAC-STARR-seq lymphoblastoid active region 6841 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98503593..98503902) | | |
| ID: 130008515 | ATAC-STARR-seq lymphoblastoid active region 6840 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98469103..98469472) | | |
| ID: 130008514 | ATAC-STARR-seq lymphoblastoid silent region 4751 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98457003..98457212) | | |
| ID: 130008513 | ATAC-STARR-seq lymphoblastoid silent region 4750 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98401549..98401608) | | |
| ID: 129663207 | ReSE screen-validated silencer GRCh37_chr12:98857507-98857880 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98463729..98464102) | | |
| ID: 127824809 | OCT4-NANOG hESC enhancer GRCh37_chr12:98779458-98779959 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98385680..98386181) | | |
| ID: 126861608 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr12:98792630-98793829 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98398852..98400051) | | |
| ID: 126861607 | MED14-independent group 3 enhancer GRCh37_chr12:98738483-98739682 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98344705..98345904) | | |
| ID: 126861606 | BRD4-independent group 4 enhancer GRCh37_chr12:98734685-98735884 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98340907..98342106) | | |
| ID: 124902994 | uncharacterized LOC124902994 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98474550..98476995, complement) | | |
| ID: 124646387 | Sharpr-MPRA regulatory region 8350 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98490531..98490825) | | |
| ID: 106481184 | RNA, U4 small nuclear 41, pseudogene [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98417896..98418038, complement) | | |
| ID: 105369933 | uncharacterized LOC105369933 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98337659..98350717, complement) | | |
| ID: 100189207 | tRNA-Asp (anticodon GTC) 1-1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98503503..98503574) | TRNAD10 | |
| ID: 100189171 | tRNA-Trp (anticodon CCA) 4-1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98504252..98504323) | TRNAW5 | |
| ID: 643770 | long intergenic non-protein coding RNA 2453 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98485544..98503855, complement) | | |
| ID: 121456 | solute carrier family 9 member 7 pseudogene 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (98453840..98457145, complement) | | |