| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:83034885-83035228 | Common:1; Rare:85 | ||||
| chr4:83455809-83456087 | Common:2; Rare:111 | ||||
| chr4:86359962-86360347 | Common:1; Rare:73; Clinvar:3; Clinvar (benign):3 | ||||
| chr4:87422537-87422640 | Common:1; Rare:30 | ||||
| chr4:88284690-88284936 | Common:2; Rare:66 | ||||
| chr4:88523738-88523836 | Common:2; Rare:32 | ||||
| chr4:88697799-88697977 | Common:2; Rare:47 | ||||
| chr4:89111272-89111597 | Common:4; Rare:127 | ||||
| chr4:94207562-94207904 | Common:1; Rare:97 | ||||
| chr4:94451792-94451993 | Common:3; Rare:64 | ||||
| chr4:98929036-98929365 | Common:3; Rare:98 | ||||
| chr4:98995457-98995756 | Common:6; Rare:110 | ||||
| chr4:99088696-99088857 | Common:5; Rare:71 | ||||
| chr4:99563995-99564191 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:99816555-99816877 | Common:1; Rare:52 |