Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151281994-151282318 | Rare:90 | ||||
chr1:151327667-151327820 | Common:2; Rare:34 | ||||
chr1:151346839-151347029 | Rare:54 | ||||
chr1:151347239-151347487 | Rare:60 | ||||
chr1:151399480-151399597 | Common:1; Rare:41; Clinvar (pathogenic):1 | ||||
chr1:151511150-151511397 | Common:3; Rare:55 | ||||
chr1:151716782-151717085 | Common:1; Rare:85 | ||||
chr1:151763457-151763515 | Rare:23 | ||||
chr1:151790422-151790871 | Common:3; Rare:109 | ||||
chr1:151909431-151909569 | Rare:49 | ||||
chr1:153608954-153609170 | Rare:43 | ||||
chr1:153633884-153634123 | Common:4; Rare:74 | ||||
chr1:153727758-153728078 | Common:1; Rare:97 | ||||
chr1:153958571-153958862 | Common:1; Rare:90 | ||||
chr1:153963504-153963719 | Common:1; Rare:56 |