| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:105895335-105895515 | Rare:49 | ||||
| chr4:106316055-106316166 | Rare:29 | ||||
| chr4:106316173-106316625 | Common:5; Rare:144 | ||||
| chr4:107720165-107720493 | Common:7; Rare:133 | ||||
| chr4:107824461-107824568 | Rare:19 | ||||
| chr4:107824597-107824740 | Rare:30 | ||||
| chr4:107824772-107825044 | Common:1; Rare:78 | ||||
| chr4:107825583-107825743 | Common:1; Rare:18 | ||||
| chr4:107989651-107990038 | Common:6; Rare:164; Clinvar:5; Clinvar (benign):5 | ||||
| chr4:108620384-108620647 | Common:6; Rare:134 | ||||
| chr4:109433756-109433913 | Common:1; Rare:56 | ||||
| chr4:109730015-109730242 | Common:3; Rare:59 | ||||
| chr4:109815464-109815798 | Common:1; Rare:89 | ||||
| chr4:110476048-110476399 | Common:1; Rare:75 | ||||
| chr4:112145291-112145495 | Common:1; Rare:53 |