| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:106316173-106316617 | Common:5; Rare:142 | ||||
| chr4:107720181-107720496 | Common:7; Rare:129 | ||||
| chr4:107824323-107824739 | Common:1; Rare:81 | ||||
| chr4:107824778-107825089 | Common:1; Rare:95 | ||||
| chr4:107989679-107989948 | Common:6; Rare:117; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620393-108620636 | Common:6; Rare:121 | ||||
| chr4:109815260-109815553 | Common:2; Rare:81 | ||||
| chr4:112285761-112285994 | Rare:73 | ||||
| chr4:112637038-112637182 | Common:1; Rare:42 | ||||
| chr4:112637392-112637570 | Common:3; Rare:47 | ||||
| chr4:113761129-113761375 | Common:1; Rare:55 | ||||
| chr4:113979598-113979837 | Common:6; Rare:55 | ||||
| chr4:118685318-118685560 | Common:2; Rare:68 | ||||
| chr4:119212355-119212860 | Common:5; Rare:142 | ||||
| chr4:119213109-119213338 | Rare:34 |