| ID: 127399264 | H3K4me1 hESC enhancer GRCh37_chr3:182517161-182517661 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (182799373..182799873) | | |
| ID: 127399263 | H3K4me1 hESC enhancer GRCh37_chr3:182516660-182517160 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (182798872..182799372) | | |
| ID: 123453199 | Sharpr-MPRA regulatory region 857 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (182802421..182802715) | | |
| ID: 115995535 | CRISPRi-validated cis-regulatory element chr3.5108 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (182715178..182715267) | | |
| ID: 105374246 | uncharacterized LOC105374246 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (182980807..182986733) | | |
| ID: 105374245 | ATP11B divergent transcript [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (182782599..182793364, complement) | | |
| ID: 100505642 | C9orf85 pseudogene 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (182955038..182955593, complement) | | |
| ID: 100422200 | EIF3E pseudogene 4 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (182843573..182844620, complement) | | |
| ID: 54165 | defective in cullin neddylation 1 domain containing 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (182938074..182985918, complement) | DCNL1, DCUN1L1, RP42, SCCRO, SCRO, Tes3 | 605905 |
| ID: 23200 | ATPase phospholipid transporting 11B (putative) [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (182793504..182921629) | ATPIF, ATPIR | 605869 |