ID: 124906309 | uncharacterized LOC124906309 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (183030584..183033984, complement) | | |
ID: 123453199 | Sharpr-MPRA regulatory region 857 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (182802421..182802715) | | |
ID: 105374247 | uncharacterized LOC105374247 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (183108225..183114253) | | |
ID: 105374246 | uncharacterized LOC105374246 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (182980807..182986733) | | |
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: 56922 | methylcrotonyl-CoA carboxylase subunit 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (183015218..183116196, complement) | MCC-B, MCCA, MCCCalpha | 609010 |
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 |