| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:9690610-9690844 | Common:3; Rare:52 | ||||
| chr4:9691421-9691564 | Common:1; Rare:48 | ||||
| chr4:9707200-9707600 | Common:8; Rare:162 | ||||
| chr4:10006140-10006510 | Common:3; Rare:89 | ||||
| chr4:10122337-10122501 | Common:4; Rare:76 | ||||
| chr4:10297230-10297690 | Rare:134 | ||||
| chr4:12026969-12027369 | Common:11; Rare:183 | ||||
| chr4:12732970-12733590 | Common:4; Rare:112 | ||||
| chr4:12903118-12903430 | Common:3; Rare:63 | ||||
| chr4:13298644-13299072 | Common:6; Rare:274 | ||||
| chr4:13544238-13544450 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:13703193-13703437 | Common:2; Rare:44 | ||||
| chr4:14879587-14880087 | Common:21; Rare:225 | ||||
| chr4:15000996-15001480 | Common:4; Rare:140 | ||||
| chr4:15004791-15005104 | Common:4; Rare:189 |