| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:124712121-124712530 | Common:1; Rare:106 | ||||
| chr4:124712658-124713110 | Common:1; Rare:136 | ||||
| chr4:127632864-127633035 | Rare:48 | ||||
| chr4:127782010-127782432 | Common:2; Rare:120 | ||||
| chr4:127782446-127782647 | Common:1; Rare:61 | ||||
| chr4:127782649-127782811 | Common:1; Rare:36 | ||||
| chr4:127782953-127783257 | Common:1; Rare:45 | ||||
| chr4:127880677-127881073 | Common:1; Rare:120 | ||||
| chr4:127881151-127881642 | Common:1; Rare:143 | ||||
| chr4:127964776-127964801 | Rare:5 | ||||
| chr4:127965076-127965495 | Common:2; Rare:137; Clinvar:7; Clinvar (benign):3 | ||||
| chr4:127965501-127965622 | Common:3; Rare:29 | ||||
| chr4:127965629-127965653 | Rare:4 | ||||
| chr4:127965669-127965729 | Rare:17 | ||||
| chr4:127965905-127966029 | Common:1; Rare:27; Clinvar (benign):1 |