| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:94162366-94162656 | Common:2; Rare:53 | ||||
| chr4:94226422-94226482 | Common:1; Rare:6 | ||||
| chr4:94226861-94227135 | Common:2; Rare:73 | ||||
| chr4:94295790-94296019 | Common:1; Rare:62 | ||||
| chr4:103554274-103554276 | |||||
| chr4:103555992-103556278 | Common:3; Rare:69 | ||||
| chr4:103719160-103719253 | Rare:28; Clinvar (pathogenic):1 | ||||
| chr4:103946635-103946933 | Common:3; Rare:63 | ||||
| chr4:107932183-107932511 | Common:3; Rare:67 | ||||
| chr4:110057572-110057850 | Rare:57 | ||||
| chr4:110196314-110196531 | Common:4; Rare:76 | ||||
| chr4:110197041-110197153 | Common:2; Rare:35 | ||||
| chr4:110197602-110197713 | Common:1; Rare:22 | ||||
| chr4:112086930-112087232 | Common:3; Rare:73 | ||||
| chr4:112645587-112646206 | Common:5; Rare:169 |