Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99659423-99659552 | Rare:36 | ||||
chr10:99732076-99732273 | Rare:63; Clinvar:3 | ||||
chr10:100185898-100186152 | Rare:92 | ||||
chr10:100286642-100286750 | Common:3; Rare:56 | ||||
chr10:100987429-100987560 | Rare:55 | ||||
chr10:101031093-101031295 | Common:1; Rare:48 | ||||
chr10:101035836-101036029 | Common:1; Rare:41 | ||||
chr10:102394321-102394623 | Common:1; Rare:76 | ||||
chr10:102395552-102395769 | Common:1; Rare:54 | ||||
chr10:102400694-102401014 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):2 | ||||
chr10:102645102-102645241 | Rare:39 | ||||
chr10:102714274-102714627 | Common:2; Rare:118 | ||||
chr10:103193240-103193587 | Common:5; Rare:88; Clinvar (benign):1 | ||||
chr10:103396442-103396719 | Rare:97 | ||||
chr10:104121838-104122139 | Common:1; Rare:90 |