Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99659271-99659515 | Common:1; Rare:60 | ||||
chr10:99732076-99732308 | Rare:81; Clinvar:3 | ||||
chr10:100186014-100186162 | Rare:46 | ||||
chr10:100535858-100535949 | Common:6; Rare:49 | ||||
chr10:100912663-100912981 | Common:1; Rare:93 | ||||
chr10:100987452-100987557 | Rare:41 | ||||
chr10:101031132-101031264 | Rare:32 | ||||
chr10:101588217-101588328 | Rare:46 | ||||
chr10:102714271-102714636 | Common:2; Rare:122 | ||||
chr10:103193247-103193532 | Common:5; Rare:81; Clinvar (benign):1 | ||||
chr10:103351050-103351188 | Common:1; Rare:52 | ||||
chr10:103396417-103396677 | Rare:94 | ||||
chr10:110006006-110006106 | Common:2; Rare:25 | ||||
chr10:110007687-110008009 | Rare:95 | ||||
chr10:110919348-110919629 | Common:7; Rare:77 |