| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:105708641-105708859 | Common:2; Rare:72 | ||||
| chr4:105895237-105895521 | Rare:84 | ||||
| chr4:106316073-106316108 | Rare:8 | ||||
| chr4:106316129-106316601 | Common:5; Rare:152 | ||||
| chr4:107720175-107720522 | Common:7; Rare:139 | ||||
| chr4:107824468-107824746 | Common:1; Rare:55 | ||||
| chr4:107824762-107825104 | Common:1; Rare:102 | ||||
| chr4:107989675-107990052 | Common:6; Rare:158; Clinvar:5; Clinvar (benign):5 | ||||
| chr4:108620380-108620660 | Common:6; Rare:140 | ||||
| chr4:109433750-109433819 | Common:1; Rare:26 | ||||
| chr4:109703379-109703510 | Rare:52 | ||||
| chr4:109729927-109730210 | Common:4; Rare:72 | ||||
| chr4:109815380-109815553 | Common:1; Rare:46 | ||||
| chr4:112285827-112285993 | Rare:52 | ||||
| chr4:112636879-112637193 | Common:1; Rare:87 |