| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:70838979-70839493 | Common:10; Rare:555 | ||||
| chr4:70839560-70839760 | Rare:59 | ||||
| chr4:70839893-70840321 | Common:1; Rare:243 | ||||
| chr4:70901813-70902552 | Common:37; Rare:867 | ||||
| chr4:70902685-70903085 | Common:2; Rare:104 | ||||
| chr4:70992287-70992687 | Common:4; Rare:111 | ||||
| chr4:70993160-70993846 | Common:38; Rare:853 | ||||
| chr4:72039033-72039525 | Common:8; Rare:151 | ||||
| chr4:72567670-72568320 | Common:18; Rare:802 | ||||
| chr4:72568226-72568467 | Common:2; Rare:71 | ||||
| chr4:72568378-72568799 | Common:10; Rare:304 | ||||
| chr4:72568785-72569491 | Common:9; Rare:549 | ||||
| chr4:73069030-73069220 | Rare:63 | ||||
| chr4:73069230-73069570 | Common:2; Rare:296; Clinvar (benign):3 | ||||
| chr4:73069501-73070037 | Common:12; Rare:871 |