| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102828097-102828291 | Common:3; Rare:68 | ||||
| chr4:102868850-102869063 | Common:2; Rare:72 | ||||
| chr4:105708636-105708827 | Rare:61 | ||||
| chr4:106316183-106316597 | Common:5; Rare:134 | ||||
| chr4:107720183-107720496 | Common:7; Rare:127 | ||||
| chr4:107824489-107824735 | Common:1; Rare:52 | ||||
| chr4:107824762-107825081 | Common:1; Rare:95 | ||||
| chr4:107989661-107989989 | Common:6; Rare:143; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620373-108620622 | Common:6; Rare:126 | ||||
| chr4:109815473-109815544 | Rare:22 | ||||
| chr4:112285757-112285978 | Rare:70 | ||||
| chr4:112637055-112637187 | Common:1; Rare:37 | ||||
| chr4:119212410-119212725 | Common:2; Rare:95 | ||||
| chr4:119300711-119300805 | Common:1; Rare:39 | ||||
| chr4:120066819-120066964 | Common:4; Rare:38 |