| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102827442-102828135 | Common:4; Rare:230 | ||||
| chr4:102868850-102869063 | Common:2; Rare:72 | ||||
| chr4:103076303-103076311 | Rare:3 | ||||
| chr4:105552523-105552880 | Common:1; Rare:74 | ||||
| chr4:105708641-105708922 | Common:3; Rare:85 | ||||
| chr4:105895349-105895515 | Rare:44 | ||||
| chr4:106316135-106316171 | Rare:12 | ||||
| chr4:106316185-106316617 | Common:5; Rare:141 | ||||
| chr4:107720175-107720533 | Common:7; Rare:146 | ||||
| chr4:107824468-107824746 | Common:1; Rare:55 | ||||
| chr4:107824778-107825029 | Common:1; Rare:67 | ||||
| chr4:107989661-107989935 | Common:6; Rare:121; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620390-108620615 | Common:6; Rare:112 | ||||
| chr4:109433757-109433954 | Common:1; Rare:65 | ||||
| chr4:109730044-109730249 | Common:2; Rare:51 |