| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:82900906-82901023 | Rare:45 | ||||
| chr4:83010745-83010914 | Rare:28 | ||||
| chr4:83455787-83456156 | Common:2; Rare:145 | ||||
| chr4:83485082-83485287 | Common:3; Rare:86 | ||||
| chr4:84966633-84966746 | Rare:30 | ||||
| chr4:84966831-84967036 | Rare:55 | ||||
| chr4:85827650-85827943 | Common:1; Rare:43 | ||||
| chr4:86357716-86357732 | Rare:2 | ||||
| chr4:86358441-86358596 | Rare:27 | ||||
| chr4:86359935-86360185 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:86594055-86594361 | Rare:99 | ||||
| chr4:86934810-86935108 | Common:2; Rare:119 | ||||
| chr4:86936177-86936330 | Rare:35 | ||||
| chr4:87006879-87006956 | Common:1; Rare:25 | ||||
| chr4:87007150-87007350 | Common:1; Rare:74 |