| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:18022113-18022352 | Common:3; Rare:68 | ||||
| chr4:20700264-20700497 | Common:1; Rare:179 | ||||
| chr4:22515988-22516270 | Common:7; Rare:176 | ||||
| chr4:23889946-23890261 | Common:1; Rare:75 | ||||
| chr4:24584462-24584718 | Common:2; Rare:155 | ||||
| chr4:25160365-25160727 | Common:6; Rare:210; Clinvar:4; Clinvar (benign):2 | ||||
| chr4:25233808-25234119 | Rare:224 | ||||
| chr4:25312557-25312910 | Common:4; Rare:132 | ||||
| chr4:25376973-25377369 | Common:6; Rare:232 | ||||
| chr4:25914038-25914328 | Common:4; Rare:232 | ||||
| chr4:25914330-25914640 | Common:1; Rare:115 | ||||
| chr4:26319447-26319749 | Rare:150 | ||||
| chr4:26320320-26320850 | Common:3; Rare:255 | ||||
| chr4:26320874-26321090 | Rare:121; Clinvar (benign):2 | ||||
| chr4:26583941-26584131 | Rare:68 |