Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:26912571-26912753 | Rare:35 | ||||
chr2:27070659-27070953 | Rare:55 | ||||
chr2:27081116-27081448 | Common:7; Rare:60 | ||||
chr2:27207133-27207313 | Rare:44 | ||||
chr2:28533369-28533556 | Common:2; Rare:38 | ||||
chr2:29920483-29920693 | Common:3; Rare:81; Clinvar:16; Clinvar (benign):15 | ||||
chr2:30421855-30421978 | Rare:29 | ||||
chr2:30679790-30680025 | Rare:46 | ||||
chr2:31142243-31142390 | Rare:21 | ||||
chr2:32357946-32358130 | Common:2; Rare:30 | ||||
chr2:39666890-39667106 | Rare:57 | ||||
chr2:44935752-44936092 | Common:1; Rare:73 | ||||
chr2:46494004-46494162 | Common:2; Rare:32 | ||||
chr2:46500224-46500462 | Common:3; Rare:57 | ||||
chr2:47226760-47226917 | Common:4; Rare:28 |