| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:2800957-2801144 | Common:2; Rare:63 | ||||
| chr4:2801325-2801398 | Rare:23 | ||||
| chr4:2801630-2801641 | Rare:1 | ||||
| chr4:2813030-2813143 | Common:2; Rare:17 | ||||
| chr4:2832643-2832829 | Common:2; Rare:57 | ||||
| chr4:2835246-2835455 | Common:1; Rare:37; Clinvar (benign):2 | ||||
| chr4:2936144-2936238 | Rare:21 | ||||
| chr4:2936960-2937057 | Rare:32 | ||||
| chr4:2937288-2937580 | Common:2; Rare:85 | ||||
| chr4:2937886-2938057 | Common:1; Rare:45 | ||||
| chr4:2962799-2962826 | Rare:5 | ||||
| chr4:3013852-3014107 | Common:3; Rare:59 | ||||
| chr4:3040338-3040360 | Rare:5 | ||||
| chr4:3040502-3040660 | Common:1; Rare:51 | ||||
| chr4:3041175-3041369 | Common:1; Rare:32 |