Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:196318184-196318328 | Common:1; Rare:63 | ||||
chr3:196503689-196503952 | Common:5; Rare:91 | ||||
chr3:196568506-196568679 | Common:3; Rare:47 | ||||
chr3:196867748-196867946 | Rare:67 | ||||
chr3:196942390-196942680 | Common:1; Rare:119 | ||||
chr3:197029800-197029961 | Common:1; Rare:51 | ||||
chr3:197736838-197737128 | Common:3; Rare:92 | ||||
chr3:197749777-197749974 | Common:1; Rare:77 | ||||
chr3:197949893-197950230 | Common:4; Rare:101; Clinvar (benign):1 | ||||
chr3:197959986-197960277 | Common:1; Rare:111 | ||||
chr4:337470-337833 | Common:1; Rare:94 | ||||
chr4:499141-499307 | Common:2; Rare:61 | ||||
chr4:663576-663725 | Rare:48 | ||||
chr4:674237-674577 | Common:2; Rare:160 | ||||
chr4:705578-705851 | Rare:89 |