Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:125916344-125916615 | Common:4; Rare:81 | ||||
chr3:150408884-150409161 | Rare:72 | ||||
chr3:151770125-151770437 | Common:3; Rare:47 | ||||
chr3:153163290-153163591 | Rare:73 | ||||
chr3:156543241-156543532 | Common:2; Rare:68 | ||||
chr3:158653157-158653389 | Rare:52; Clinvar:1 | ||||
chr3:169765053-169765209 | Rare:68; Clinvar (pathogenic):2 | ||||
chr3:171874324-171874557 | Common:3; Rare:42 | ||||
chr3:185658606-185658857 | Common:1; Rare:51 | ||||
chr3:194583866-194584027 | Common:11; Rare:56 | ||||
chr3:195147556-195147859 | Common:2; Rare:58 | ||||
chr3:195990254-195990459 | Rare:26 | ||||
chr3:197627833-197628049 | Common:7; Rare:82 | ||||
chr4:3041559-3041828 | Common:4; Rare:64 | ||||
chr4:3955417-3955673 | Common:8; Rare:75 |