Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102743620-102744056 | Common:3; Rare:118 | ||||
chr10:102776078-102776202 | Common:1; Rare:18 | ||||
chr10:102854191-102854310 | Rare:49 | ||||
chr10:103193247-103193338 | Common:5; Rare:34; Clinvar (benign):1 | ||||
chr10:103277018-103277168 | Rare:44 | ||||
chr10:103350893-103351195 | Common:2; Rare:122 | ||||
chr10:103396419-103396699 | Rare:101 | ||||
chr10:103452392-103452415 | Rare:4 | ||||
chr10:103918126-103918436 | Common:4; Rare:82 | ||||
chr10:104121707-104122171 | Common:4; Rare:152 | ||||
chr10:104232308-104232508 | Common:1; Rare:53 | ||||
chr10:104268935-104269193 | Common:3; Rare:61 | ||||
chr10:104353555-104353793 | Common:2; Rare:62 | ||||
chr10:109923423-109923661 | Common:2; Rare:91 | ||||
chr10:110005942-110006108 | Common:3; Rare:47 |