| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:151015210-151015377 | Rare:47 | ||||
| chr4:151015709-151015872 | Rare:77 | ||||
| chr4:151099563-151099728 | Common:3; Rare:73 | ||||
| chr4:151226361-151226560 | Rare:36 | ||||
| chr4:151227759-151228072 | Common:1; Rare:45 | ||||
| chr4:151408842-151409307 | Common:6; Rare:138 | ||||
| chr4:152352694-152352956 | Rare:66 | ||||
| chr4:152536047-152536269 | Rare:83 | ||||
| chr4:152779611-152780169 | Common:3; Rare:133 | ||||
| chr4:153789081-153789205 | Rare:21 | ||||
| chr4:156971109-156971219 | Rare:14 | ||||
| chr4:156971773-156971945 | Common:1; Rare:63 | ||||
| chr4:158172986-158173068 | Rare:19 | ||||
| chr4:158671830-158672444 | Common:5; Rare:163; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:158723211-158723449 | Common:2; Rare:102 |