Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:119651210-119651397 | Common:5; Rare:77; Clinvar:1; Clinvar (benign):3 | ||||
chr10:119892548-119892793 | Common:3; Rare:92 | ||||
chr10:120851209-120851453 | Common:5; Rare:94 | ||||
chr10:121927890-121928069 | Common:1; Rare:67 | ||||
chr10:121928418-121928515 | Rare:30 | ||||
chr10:121974690-121974867 | Common:2; Rare:53 | ||||
chr10:122019111-122019272 | Rare:38 | ||||
chr10:122019470-122019867 | Common:5; Rare:62 | ||||
chr10:122375194-122375431 | Common:2; Rare:64 | ||||
chr10:122879532-122879691 | Common:3; Rare:44 | ||||
chr10:122954185-122954484 | Rare:110 | ||||
chr10:123008767-123009028 | Common:6; Rare:71; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124092392-124092539 | Rare:46 | ||||
chr10:124093497-124093684 | Common:2; Rare:32 | ||||
chr10:124418875-124419103 | Common:5; Rare:106; Clinvar:4; Clinvar (benign):1 |