| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15681458-15681869 | Common:3; Rare:142 | ||||
| chr4:15703011-15703157 | Common:1; Rare:41 | ||||
| chr4:16082437-16082594 | Common:1; Rare:28 | ||||
| chr4:16083239-16083428 | Common:3; Rare:43 | ||||
| chr4:16083566-16083744 | Common:2; Rare:40 | ||||
| chr4:16083879-16084196 | Common:2; Rare:86 | ||||
| chr4:16084414-16084495 | Rare:8 | ||||
| chr4:17577273-17577550 | Common:1; Rare:125 | ||||
| chr4:17614548-17614660 | Common:2; Rare:49 | ||||
| chr4:17810598-17811035 | Common:3; Rare:130 | ||||
| chr4:20700379-20700502 | Common:1; Rare:62 | ||||
| chr4:23889907-23890179 | Rare:49 | ||||
| chr4:24584322-24584725 | Common:1; Rare:127 | ||||
| chr4:25160349-25160732 | Common:3; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25234112 | Rare:109 |