Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102394321-102394563 | Rare:68 | ||||
chr10:102395561-102395735 | Common:1; Rare:49 | ||||
chr10:102502652-102502890 | Common:1; Rare:79 | ||||
chr10:102714197-102714653 | Common:2; Rare:149 | ||||
chr10:102776078-102776269 | Common:1; Rare:31 | ||||
chr10:102869403-102869551 | Common:5; Rare:31 | ||||
chr10:103193243-103193429 | Common:5; Rare:61; Clinvar (benign):1 | ||||
chr10:103350939-103351195 | Common:2; Rare:105 | ||||
chr10:103396411-103396724 | Rare:109 | ||||
chr10:103451341-103451451 | Rare:16 | ||||
chr10:103452262-103452431 | Rare:52 | ||||
chr10:104121878-104122174 | Common:2; Rare:95 | ||||
chr10:104268956-104269193 | Common:3; Rare:56 | ||||
chr10:104338463-104338512 | Rare:12 | ||||
chr10:109923423-109923600 | Common:1; Rare:63 |