| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56435967-56436329 | Rare:247 | ||||
| chr4:56467437-56467689 | Common:4; Rare:149; Clinvar (benign):8 | ||||
| chr4:56468100-56468440 | Common:1; Rare:108 | ||||
| chr4:56908852-56909014 | Common:4; Rare:90 | ||||
| chr4:56977535-56977786 | Common:2; Rare:94 | ||||
| chr4:67545423-67545724 | Common:4; Rare:140 | ||||
| chr4:67701070-67701423 | Common:8; Rare:289 | ||||
| chr4:68349956-68350248 | Common:4; Rare:198 | ||||
| chr4:70688166-70688611 | Common:4; Rare:219 | ||||
| chr4:70704604-70704822 | Common:1; Rare:70 | ||||
| chr4:70839160-70839540 | Common:4; Rare:273 | ||||
| chr4:70839824-70839931 | Common:1; Rare:53 | ||||
| chr4:70902216-70902478 | Common:8; Rare:141 | ||||
| chr4:70993280-70993801 | Common:12; Rare:236 | ||||
| chr4:73069630-73069888 | Common:3; Rare:235 |