| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56435473-56435765 | Common:5; Rare:106 | ||||
| chr4:56467521-56467684 | Common:2; Rare:69; Clinvar (benign):4 | ||||
| chr4:56656514-56656663 | Common:1; Rare:25 | ||||
| chr4:56977111-56977294 | Common:3; Rare:81 | ||||
| chr4:56977352-56977780 | Common:3; Rare:155 | ||||
| chr4:67545341-67545726 | Common:2; Rare:93 | ||||
| chr4:67701115-67701419 | Common:4; Rare:140 | ||||
| chr4:69760499-69760758 | Rare:47 | ||||
| chr4:70688176-70688599 | Common:2; Rare:106 | ||||
| chr4:70704562-70704825 | Common:1; Rare:84 | ||||
| chr4:70839232-70839394 | Common:2; Rare:63 | ||||
| chr4:70902206-70902382 | Common:4; Rare:65 | ||||
| chr4:70993327-70993701 | Common:5; Rare:106 | ||||
| chr4:71187055-71187412 | Common:2; Rare:104 | ||||
| chr4:73069684-73069888 | Common:1; Rare:92 |