Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45750581-45750830 | Rare:91 | ||||
chr1:46198342-46198503 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr1:46247321-46247779 | Common:4; Rare:86 | ||||
chr1:46303129-46303742 | Common:3; Rare:180 | ||||
chr1:46340699-46340821 | Common:3; Rare:36 | ||||
chr1:46668336-46668596 | Common:2; Rare:77 | ||||
chr1:47314043-47314479 | Common:3; Rare:93; Clinvar:3 | ||||
chr1:47333794-47333963 | Common:1; Rare:61 | ||||
chr1:50960113-50960277 | Rare:55 | ||||
chr1:50970004-50970256 | Rare:43 | ||||
chr1:51744730-51745027 | Rare:62 | ||||
chr1:51789394-51789654 | Rare:78 | ||||
chr1:51878276-51878421 | Rare:54 | ||||
chr1:51878446-51878533 | Rare:31 | ||||
chr1:51878634-51878805 | Common:1; Rare:54 |