| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:109433732-109433998 | Common:1; Rare:92 | ||||
| chr4:109560075-109560424 | Common:5; Rare:102 | ||||
| chr4:109560867-109560998 | Common:1; Rare:32 | ||||
| chr4:109815399-109815842 | Common:2; Rare:110 | ||||
| chr4:110198504-110198672 | Rare:47 | ||||
| chr4:112145293-112145516 | Common:1; Rare:62 | ||||
| chr4:112231591-112231844 | Common:2; Rare:78 | ||||
| chr4:112232148-112232276 | Common:1; Rare:51 | ||||
| chr4:112285761-112285956 | Rare:59 | ||||
| chr4:112636839-112637237 | Common:2; Rare:108 | ||||
| chr4:112637394-112637573 | Common:3; Rare:48 | ||||
| chr4:113761115-113761439 | Common:2; Rare:71 | ||||
| chr4:113978997-113979426 | Common:5; Rare:79 | ||||
| chr4:113979562-113979859 | Common:6; Rare:68 | ||||
| chr4:118352653-118352904 | Common:2; Rare:89; Clinvar:2; Clinvar (benign):3 |