| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107824485-107824564 | Rare:13 | ||||
| chr4:107824591-107824740 | Rare:32 | ||||
| chr4:107824793-107825035 | Common:1; Rare:68 | ||||
| chr4:107989690-107989935 | Common:5; Rare:111; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620393-108620647 | Common:6; Rare:128 | ||||
| chr4:112285827-112285986 | Rare:48 | ||||
| chr4:112637039-112637182 | Common:1; Rare:42 | ||||
| chr4:112637390-112637570 | Common:3; Rare:47 | ||||
| chr4:118352979-118353111 | Rare:44 | ||||
| chr4:118685243-118685458 | Common:3; Rare:70 | ||||
| chr4:119212496-119212767 | Common:4; Rare:81 | ||||
| chr4:119213141-119213294 | Rare:23 | ||||
| chr4:120066838-120066955 | Common:3; Rare:30 | ||||
| chr4:121801228-121801394 | Common:2; Rare:57 | ||||
| chr4:122732432-122732764 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 |