Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100912667-100912996 | Common:1; Rare:98 | ||||
chr10:100987229-100987621 | Common:2; Rare:138; Clinvar:1; Clinvar (benign):2 | ||||
chr10:101031136-101031268 | Rare:32 | ||||
chr10:101229445-101229701 | Common:1; Rare:59 | ||||
chr10:101588166-101588333 | Rare:70 | ||||
chr10:102394348-102394531 | Rare:50 | ||||
chr10:102395604-102395735 | Rare:35 | ||||
chr10:102502600-102502962 | Common:1; Rare:104 | ||||
chr10:102714271-102714637 | Common:2; Rare:122 | ||||
chr10:102776078-102776379 | Common:1; Rare:69 | ||||
chr10:102854191-102854289 | Rare:37 | ||||
chr10:103193240-103193584 | Common:5; Rare:88; Clinvar (benign):1 | ||||
chr10:103367872-103367985 | Common:2; Rare:18 | ||||
chr10:103396411-103396709 | Rare:106 | ||||
chr10:103452273-103452682 | Rare:100 |