| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:743862-743946 | Rare:12 | ||||
| chr4:932070-932492 | Common:2; Rare:155 | ||||
| chr4:986920-987234 | Common:4; Rare:103; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:1113518-1113637 | Common:2; Rare:41 | ||||
| chr4:1171170-1171360 | Common:2; Rare:86 | ||||
| chr4:1172767-1173037 | Common:4; Rare:42 | ||||
| chr4:1346989-1347213 | Common:3; Rare:65 | ||||
| chr4:1720323-1720638 | Common:2; Rare:92 | ||||
| chr4:1723227-1723551 | Common:4; Rare:89 | ||||
| chr4:1856095-1856427 | Rare:85 | ||||
| chr4:1976314-1976501 | Rare:44 | ||||
| chr4:1986151-1986335 | Rare:57 | ||||
| chr4:2041901-2042028 | Common:1; Rare:48 | ||||
| chr4:2468853-2469167 | Common:4; Rare:115 | ||||
| chr4:2843721-2844014 | Common:3; Rare:99 |