| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107989663-107989907 | Common:6; Rare:112; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620397-108620647 | Common:6; Rare:126 | ||||
| chr4:109433750-109433942 | Common:1; Rare:62 | ||||
| chr4:109730063-109730218 | Common:2; Rare:33 | ||||
| chr4:110475953-110476279 | Common:1; Rare:58 | ||||
| chr4:112297200-112297412 | Common:1; Rare:35 | ||||
| chr4:112636880-112637184 | Common:1; Rare:85 | ||||
| chr4:112637375-112637570 | Common:3; Rare:53 | ||||
| chr4:113979602-113979837 | Common:6; Rare:53 | ||||
| chr4:118685291-118685450 | Common:3; Rare:51 | ||||
| chr4:118836039-118836208 | Common:1; Rare:36 | ||||
| chr4:118888721-118888999 | Common:1; Rare:74 | ||||
| chr4:119212516-119212772 | Common:4; Rare:71 | ||||
| chr4:119300497-119300928 | Common:2; Rare:190 | ||||
| chr4:120066769-120066977 | Common:4; Rare:61 |