| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:119514506-119514555 | Common:1; Rare:6 | ||||
| chr4:121669676-121669987 | Common:3; Rare:86 | ||||
| chr4:128060662-128060732 | Rare:12 | ||||
| chr4:139083165-139083187 | Rare:9 | ||||
| chr4:148412043-148412098 | Rare:11 | ||||
| chr4:148445307-148445602 | Common:2; Rare:89 | ||||
| chr4:150579881-150580146 | Common:1; Rare:58 | ||||
| chr4:151100797-151101158 | Rare:74 | ||||
| chr4:151105120-151105405 | Common:7; Rare:60 | ||||
| chr4:151324569-151324840 | Common:1; Rare:50 | ||||
| chr4:158705979-158706354 | Rare:95; Clinvar:2; Clinvar (pathogenic):4 | ||||
| chr4:159102890-159103163 | Common:3; Rare:104 | ||||
| chr4:165331052-165331177 | Common:2; Rare:19 | ||||
| chr4:169213974-169214111 | Rare:26 | ||||
| chr4:184348809-184349050 | Rare:49 |