| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99088680-99088950 | Common:7; Rare:124 | ||||
| chr4:99089092-99089273 | Common:1; Rare:27 | ||||
| chr4:99563367-99563783 | Common:3; Rare:107 | ||||
| chr4:99564001-99564192 | Common:2; Rare:62; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:99894391-99894649 | Common:3; Rare:86 | ||||
| chr4:99946542-99946674 | Rare:52 | ||||
| chr4:99950228-99950725 | Rare:130 | ||||
| chr4:101347033-101347207 | Common:2; Rare:46 | ||||
| chr4:101347498-101347786 | Common:4; Rare:86 | ||||
| chr4:101348021-101348175 | Rare:41 | ||||
| chr4:102344790-102345205 | Common:3; Rare:138 | ||||
| chr4:102500998-102501285 | Common:1; Rare:85 | ||||
| chr4:102501300-102501621 | Common:1; Rare:120 | ||||
| chr4:102501841-102501971 | Common:2; Rare:36 | ||||
| chr4:102502198-102502446 | Common:7; Rare:70 |