| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102760927-102761067 | Rare:48; Clinvar:1 | ||||
| chr4:102826758-102826928 | Rare:45 | ||||
| chr4:102827443-102827890 | Common:4; Rare:147 | ||||
| chr4:102827900-102828137 | Rare:77 | ||||
| chr4:102868854-102869083 | Common:2; Rare:79 | ||||
| chr4:105145753-105145967 | Common:1; Rare:44 | ||||
| chr4:105552534-105552725 | Rare:30 | ||||
| chr4:105708636-105708827 | Rare:61 | ||||
| chr4:106316173-106316593 | Common:5; Rare:132 | ||||
| chr4:107824751-107825029 | Common:1; Rare:70 | ||||
| chr4:107989679-107989870 | Common:5; Rare:83; Clinvar:2; Clinvar (benign):4 | ||||
| chr4:108620380-108620647 | Common:6; Rare:135 | ||||
| chr4:109433750-109433926 | Common:1; Rare:59 | ||||
| chr4:109815414-109815553 | Rare:40 | ||||
| chr4:112231582-112231831 | Common:2; Rare:79 |