Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100267616-100267793 | Common:3; Rare:51 | ||||
chr10:100346828-100347179 | Rare:82 | ||||
chr10:100987439-100987584 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101031113-101031264 | Common:1; Rare:34 | ||||
chr10:101588211-101588329 | Rare:48 | ||||
chr10:102132852-102133061 | Rare:48 | ||||
chr10:102394353-102394570 | Rare:60 | ||||
chr10:102432546-102432787 | Common:1; Rare:72 | ||||
chr10:102714197-102714636 | Common:2; Rare:145 | ||||
chr10:102776078-102776226 | Common:1; Rare:23 | ||||
chr10:102869414-102869551 | Common:5; Rare:29 | ||||
chr10:103396411-103396699 | Rare:103 | ||||
chr10:104268980-104269190 | Common:2; Rare:48 | ||||
chr10:109923423-109923655 | Common:2; Rare:89 | ||||
chr10:110005918-110006084 | Common:3; Rare:55 |