| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:1289544-1289979 | Common:6; Rare:747 | ||||
| chr4:1290296-1290696 | Common:4; Rare:93 | ||||
| chr4:1309320-1309743 | Common:7; Rare:209 | ||||
| chr4:1346730-1348422 | Common:43; Rare:1302; Clinvar (pathogenic):1 | ||||
| chr4:1683492-1684239 | Common:11; Rare:346 | ||||
| chr4:1684227-1684649 | Common:10; Rare:421 | ||||
| chr4:1711405-1712043 | Common:5; Rare:234 | ||||
| chr4:1712130-1712910 | Common:28; Rare:1156 | ||||
| chr4:1712910-1713558 | Common:5; Rare:184 | ||||
| chr4:1720388-1720667 | Common:2; Rare:242 | ||||
| chr4:1721089-1721576 | Common:26; Rare:628 | ||||
| chr4:1722545-1723222 | Common:11; Rare:181 | ||||
| chr4:1793013-1793413 | Common:6; Rare:428 | ||||
| chr4:1793450-1794328 | Common:6; Rare:681; Clinvar (benign):11 | ||||
| chr4:1855200-1857124 | Common:19; Rare:1513 |