| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:86593972-86594480 | Rare:354 | ||||
| chr4:86891802-86892255 | Common:10; Rare:170 | ||||
| chr4:86892277-86892444 | Common:3; Rare:75 | ||||
| chr4:86892347-86892463 | Rare:29 | ||||
| chr4:86933409-86934282 | Common:6; Rare:227 | ||||
| chr4:86934684-86935232 | Common:7; Rare:468 | ||||
| chr4:86935770-86936015 | Common:2; Rare:95 | ||||
| chr4:86936093-86936406 | Common:1; Rare:160 | ||||
| chr4:87006776-87007386 | Common:19; Rare:495 | ||||
| chr4:87240420-87240760 | Common:2; Rare:47 | ||||
| chr4:87391120-87391383 | Common:3; Rare:132 | ||||
| chr4:87422385-87422957 | Common:8; Rare:385 | ||||
| chr4:88007443-88007799 | Common:6; Rare:254; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:88008220-88008800 | Common:5; Rare:153; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr4:88158462-88158810 | Common:1; Rare:249 |