| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:108167763-108168056 | Rare:76 | ||||
| chr4:108168438-108168556 | Rare:24 | ||||
| chr4:108168728-108168785 | Rare:10 | ||||
| chr4:108168818-108168880 | Common:1; Rare:15 | ||||
| chr4:108620373-108620647 | Common:6; Rare:139 | ||||
| chr4:109433750-109433956 | Common:1; Rare:67 | ||||
| chr4:109730044-109730378 | Common:2; Rare:70 | ||||
| chr4:109815471-109815804 | Common:1; Rare:88 | ||||
| chr4:110475963-110476286 | Common:1; Rare:61 | ||||
| chr4:112231586-112231897 | Common:2; Rare:95 | ||||
| chr4:112232131-112232276 | Common:1; Rare:61 | ||||
| chr4:112285742-112285985 | Rare:75 | ||||
| chr4:112636892-112637199 | Common:1; Rare:81 | ||||
| chr4:112637390-112637570 | Common:3; Rare:47 | ||||
| chr4:113049313-113049711 | Common:1; Rare:69; Clinvar (benign):1 |