| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:128811092-128811320 | Rare:46 | ||||
| chr4:129093478-129093736 | Common:1; Rare:78 | ||||
| chr4:133149085-133149323 | Common:2; Rare:73 | ||||
| chr4:139301227-139301557 | Common:4; Rare:95 | ||||
| chr4:139302445-139302491 | Rare:17 | ||||
| chr4:139453685-139453749 | Common:2; Rare:19 | ||||
| chr4:139453774-139454327 | Common:3; Rare:162; Clinvar:11; Clinvar (benign):4 | ||||
| chr4:139556103-139556290 | Rare:46 | ||||
| chr4:139556383-139556603 | Rare:33 | ||||
| chr4:140373398-140373693 | Common:2; Rare:121 | ||||
| chr4:141636204-141636260 | Rare:10 | ||||
| chr4:141636315-141636662 | Common:3; Rare:70 | ||||
| chr4:141636769-141637135 | Common:1; Rare:79 | ||||
| chr4:143336863-143336912 | Rare:14 | ||||
| chr4:143513280-143513538 | Common:3; Rare:96 |