| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:152679942-152680097 | Rare:32 | ||||
| chr4:152779721-152780016 | Common:1; Rare:83 | ||||
| chr4:153788920-153789205 | Rare:82 | ||||
| chr4:154550366-154550530 | Rare:51 | ||||
| chr4:158172986-158173090 | Rare:20 | ||||
| chr4:158671832-158672431 | Common:5; Rare:158; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:158723315-158723439 | Common:2; Rare:58 | ||||
| chr4:165327400-165327708 | Common:2; Rare:88 | ||||
| chr4:169620335-169620702 | Common:2; Rare:130 | ||||
| chr4:169660036-169660263 | Common:1; Rare:43 | ||||
| chr4:173369802-173369935 | Common:1; Rare:45 | ||||
| chr4:173530195-173530353 | Rare:33 | ||||
| chr4:174283612-174283965 | Common:1; Rare:71 | ||||
| chr4:174522458-174522589 | Rare:42; Clinvar:1 | ||||
| chr4:176319727-176320048 | Common:4; Rare:111 |