| ID: 132090536 | Neanderthal introgressed variant-containing enhancer experimental_50884 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29430078..29430247) | | |
| ID: 132090535 | Neanderthal introgressed variant-containing enhancer experimental_50793 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29398143..29398312) | | |
| ID: 132090534 | Neanderthal introgressed variant-containing enhancer experimental_50790 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29393770..29393939) | | |
| ID: 127891120 | H3K4me1 hESC enhancer GRCh37_chr19:30059413-30059913 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29568506..29569006) | | |
| ID: 127891119 | H3K4me1 hESC enhancer GRCh37_chr19:30055952-30056800 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29565045..29565893) | | |
| ID: 127891118 | H3K4me1 hESC enhancer GRCh37_chr19:30053547-30054047 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29562640..29563140) | | |
| ID: 127891117 | H3K4me1 hESC enhancer GRCh37_chr19:30030691-30031191 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29539784..29540284) | | |
| ID: 127891116 | H3K4me1 hESC enhancer GRCh37_chr19:30030190-30030690 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29539283..29539783) | | |
| ID: 127891115 | H3K4me1 hESC enhancer GRCh37_chr19:30025281-30025781 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29534374..29534874) | | |
| ID: 127891114 | H3K4me1 hESC enhancer GRCh37_chr19:29910274-29911005 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29419367..29420098) | | |
| ID: 127891113 | H3K4me1 hESC enhancer GRCh37_chr19:29908074-29908807 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29417167..29417900) | | |
| ID: 127891112 | H3K4me1 hESC enhancer GRCh37_chr19:29895755-29896381 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29404795..29405474) | | |
| ID: 124904683 | uncharacterized LOC124904683 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29488179..29529280, complement) | | |
| ID: 113939969 | Sharpr-MPRA regulatory region 9443 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29415562..29415856) | | |
| ID: 342865 | V-set and transmembrane domain containing 2B [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29525418..29564551) | | |
| ID: 284395 | VSTM2B divergent transcript [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29287009..29525750, complement) | | |