Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:100352146-100352731 | Common:3; Rare:126 | ||||
chr1:100352816-100352987 | Common:1; Rare:59; Clinvar (benign):2 | ||||
chr1:100894625-100895065 | Common:2; Rare:101 | ||||
chr1:100895102-100895301 | Common:2; Rare:37 | ||||
chr1:100895374-100895531 | Rare:33 | ||||
chr1:100895610-100895834 | Common:2; Rare:52 | ||||
chr1:100895837-100896264 | Rare:115 | ||||
chr1:100896593-100896839 | Common:1; Rare:62 | ||||
chr1:101025313-101025375 | Rare:26 | ||||
chr1:101025700-101026002 | Common:2; Rare:82 | ||||
chr1:101026036-101026378 | Rare:58 | ||||
chr1:101236606-101237023 | Common:4; Rare:82 | ||||
chr1:103525429-103525771 | Rare:97 | ||||
chr1:103525844-103526248 | Common:1; Rare:124 | ||||
chr1:103526324-103526349 | Rare:2 |