| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:677752-678018 | Common:1; Rare:62 | ||||
| chr4:680974-681235 | Rare:100 | ||||
| chr4:932206-932492 | Common:2; Rare:112 | ||||
| chr4:986912-987159 | Common:3; Rare:82; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:1113524-1113661 | Common:3; Rare:57 | ||||
| chr4:1249976-1250038 | Common:2; Rare:11 | ||||
| chr4:1289650-1289925 | Common:1; Rare:93 | ||||
| chr4:1347131-1347216 | Common:1; Rare:22 | ||||
| chr4:1717343-1717664 | Common:2; Rare:91 | ||||
| chr4:1720538-1720602 | Rare:13 | ||||
| chr4:1723277-1723540 | Common:4; Rare:79 | ||||
| chr4:1856128-1856404 | Rare:73 | ||||
| chr4:2041912-2042022 | Common:1; Rare:44 | ||||
| chr4:2418641-2419004 | Common:4; Rare:113 | ||||
| chr4:2468853-2469200 | Common:5; Rare:140 |