| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:134201745-134201965 | Rare:48 | ||||
| chr4:137532395-137532689 | Common:2; Rare:44 | ||||
| chr4:138242295-138242627 | Common:1; Rare:71 | ||||
| chr4:139015432-139015769 | Common:2; Rare:105 | ||||
| chr4:139301291-139301562 | Common:4; Rare:84 | ||||
| chr4:139302466-139302512 | Rare:9 | ||||
| chr4:139453692-139453749 | Common:2; Rare:16 | ||||
| chr4:139453770-139454254 | Common:3; Rare:137; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556135-139556710 | Common:1; Rare:111 | ||||
| chr4:139665795-139665874 | Rare:15 | ||||
| chr4:140154071-140154284 | Common:1; Rare:84 | ||||
| chr4:140373380-140373697 | Common:2; Rare:126 | ||||
| chr4:140523926-140524231 | Common:2; Rare:94 | ||||
| chr4:141220770-141220971 | Rare:64 | ||||
| chr4:142405410-142405543 | Rare:22 |