| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:24584462-24584815 | Common:1; Rare:96 | ||||
| chr4:25159921-25160169 | Common:1; Rare:66 | ||||
| chr4:25160241-25160740 | Common:3; Rare:166; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233766-25234148 | Rare:129 | ||||
| chr4:25312504-25312899 | Common:4; Rare:140 | ||||
| chr4:25376878-25377380 | Common:4; Rare:143 | ||||
| chr4:25861024-25861144 | Common:1; Rare:33 | ||||
| chr4:25862974-25863084 | Common:1; Rare:12 | ||||
| chr4:25913999-25914436 | Common:4; Rare:177 | ||||
| chr4:26319172-26319399 | Rare:54 | ||||
| chr4:26319553-26319758 | Rare:62 | ||||
| chr4:26320135-26320467 | Common:3; Rare:75 | ||||
| chr4:26320562-26321103 | Common:1; Rare:209; Clinvar (benign):1 | ||||
| chr4:26321235-26321359 | Common:1; Rare:41 | ||||
| chr4:26583966-26584150 | Rare:38 |