| ID: 132090827 | Neanderthal introgressed variant-containing enhancer experimental_10489 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (120965267..120965436) | | |
| ID: 127819393 | H3K27ac hESC enhancer GRCh37_chr10:122784925-122785425 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (121025412..121025912) | | |
| ID: 127819392 | H3K27ac hESC enhancer GRCh37_chr10:122784424-122784924 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (121024911..121025411) | | |
| ID: 126861064 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr10:122918427-122919626 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (121158913..121160112) | | |
| ID: 126861063 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr10:122872407-122873606 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (121112893..121114092) | | |
| ID: 126861062 | BRD4-independent group 4 enhancer GRCh37_chr10:122669667-122670866 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (120910155..120911846) | | |
| ID: 124902516 | uncharacterized LOC124902516 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (121083932..121085807, complement) | | |
| ID: 124902515 | uncharacterized LOC124902515 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (121118867..121185544, complement) | | |
| ID: 111875831 | Sharpr-MPRA regulatory region 5528 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (120942856..120943150) | | |
| ID: 105378522 | uncharacterized LOC105378522 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (121129468..121155896) | | |
| ID: 105378521 | uncharacterized LOC105378521 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (120999366..121077476, complement) | | |
| ID: 105378520 | uncharacterized LOC105378520 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (120984962..120997574, complement) | | |
| ID: 105378519 | uncharacterized LOC105378519 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (120901850..120981653, complement) | | |
| ID: 101927889 | long intergenic non-protein coding RNA 1153 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (121178537..121185966) | | |
| ID: 646255 | ribosomal protein L19 pseudogene 16 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (121133016..121133754, complement) | RPL19_5_1105 | |
| ID: 55717 | WD repeat domain 11 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (120851362..120909524) | BRWD2, DR11, HH14, SRI1, WDR15 | 606417 |