| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:44678369-44678465 | Rare:29 | ||||
| chr4:44678639-44678714 | Rare:35 | ||||
| chr4:47485198-47485346 | Common:1; Rare:54 | ||||
| chr4:48016624-48016789 | Common:1; Rare:48 | ||||
| chr4:48780151-48780472 | Common:3; Rare:108 | ||||
| chr4:51842819-51843212 | Common:1; Rare:118 | ||||
| chr4:56387423-56387528 | Rare:35 | ||||
| chr4:56435568-56435746 | Common:3; Rare:63 | ||||
| chr4:56467542-56467699 | Common:2; Rare:66; Clinvar (benign):5 | ||||
| chr4:65670461-65670622 | Common:1; Rare:39 | ||||
| chr4:67701121-67701358 | Common:4; Rare:111 | ||||
| chr4:73069707-73069946 | Common:1; Rare:98 | ||||
| chr4:75514273-75514517 | Common:1; Rare:84 | ||||
| chr4:75630484-75630666 | Rare:43 | ||||
| chr4:75724390-75724713 | Common:1; Rare:89 |