| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139302480-139302546 | Rare:10 | ||||
| chr4:139453653-139453697 | Common:1; Rare:20 | ||||
| chr4:139453770-139454204 | Common:3; Rare:112; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556112-139556179 | Rare:17 | ||||
| chr4:139556181-139556622 | Rare:81 | ||||
| chr4:139556779-139556872 | Rare:14 | ||||
| chr4:139665791-139666069 | Common:2; Rare:73 | ||||
| chr4:140152985-140153129 | Rare:47 | ||||
| chr4:140153134-140153252 | Rare:41 | ||||
| chr4:140153991-140154284 | Common:2; Rare:96 | ||||
| chr4:140373358-140373696 | Common:2; Rare:133 | ||||
| chr4:141636829-141636991 | Rare:32 | ||||
| chr4:142405371-142405458 | Rare:17 | ||||
| chr4:142474378-142474511 | Rare:22 | ||||
| chr4:143184628-143185068 | Common:9; Rare:164 |