| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:705469-705953 | Common:7; Rare:601 | ||||
| chr4:932046-932660 | Common:14; Rare:1010 | ||||
| chr4:932740-933144 | Rare:175 | ||||
| chr4:973477-973877 | Common:31; Rare:455 | ||||
| chr4:986675-987590 | Common:16; Rare:1025; Clinvar:18; Clinvar (benign):5; Clinvar (pathogenic):9 | ||||
| chr4:992450-992963 | Common:6; Rare:540 | ||||
| chr4:993350-993750 | Common:25; Rare:138 | ||||
| chr4:993710-994314 | Common:15; Rare:277 | ||||
| chr4:1009645-1010045 | Common:26; Rare:174 | ||||
| chr4:1011269-1011669 | Common:18; Rare:354 | ||||
| chr4:1011929-1012335 | Common:5; Rare:272 | ||||
| chr4:1201379-1201779 | Common:1; Rare:196 | ||||
| chr4:1248309-1248478 | Common:2; Rare:106 | ||||
| chr4:1248629-1249477 | Common:43; Rare:1184 | ||||
| chr4:1249390-1250276 | Common:21; Rare:453 |