| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:149261934-149262236 | Common:2; Rare:100 | ||||
| chr7:149460831-149461252 | Common:1; Rare:70 | ||||
| chr7:149873642-149874092 | Common:5; Rare:149 | ||||
| chr7:150368938-150369140 | Common:2; Rare:54 | ||||
| chr7:150405273-150405356 | Rare:27 | ||||
| chr7:151028175-151028493 | Rare:119 | ||||
| chr7:151057834-151058205 | Common:3; Rare:106 | ||||
| chr7:151080776-151081003 | Rare:76 | ||||
| chr7:151085865-151085921 | Rare:14 | ||||
| chr7:151227138-151227411 | Common:1; Rare:78 | ||||
| chr7:151232303-151232592 | Common:1; Rare:103 | ||||
| chr7:151240111-151240375 | Common:5; Rare:69 | ||||
| chr7:151248600-151248941 | Common:2; Rare:76 | ||||
| chr7:151519891-151519993 | Rare:23 | ||||
| chr7:151632075-151632270 | Common:1; Rare:68; Clinvar:4; Clinvar (benign):6 |