| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102868850-102869083 | Common:2; Rare:83 | ||||
| chr4:103019638-103019785 | Common:1; Rare:43 | ||||
| chr4:103076295-103076594 | Common:1; Rare:91 | ||||
| chr4:105473963-105474191 | Common:5; Rare:112 | ||||
| chr4:105552421-105552696 | Rare:40 | ||||
| chr4:105708636-105708827 | Rare:61 | ||||
| chr4:106316173-106316657 | Common:5; Rare:154 | ||||
| chr4:107720166-107720505 | Common:7; Rare:137 | ||||
| chr4:107824485-107824740 | Common:1; Rare:52 | ||||
| chr4:107989679-107989927 | Common:6; Rare:114; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620357-108620711 | Common:6; Rare:160 | ||||
| chr4:109302701-109303053 | Common:5; Rare:105 | ||||
| chr4:109433750-109433836 | Common:1; Rare:31 | ||||
| chr4:109560068-109560389 | Common:5; Rare:93 | ||||
| chr4:109815458-109815798 | Common:1; Rare:90 |