| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107824672-107824749 | Rare:16 | ||||
| chr4:107989681-107989935 | Common:6; Rare:115; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620404-108620647 | Common:6; Rare:125 | ||||
| chr4:109703406-109703557 | Rare:54 | ||||
| chr4:109729835-109730195 | Common:4; Rare:96 | ||||
| chr4:112636886-112637187 | Common:1; Rare:84 | ||||
| chr4:112637394-112637570 | Common:3; Rare:47 | ||||
| chr4:113761129-113761252 | Common:1; Rare:29 | ||||
| chr4:118685318-118685440 | Common:2; Rare:40 | ||||
| chr4:119212355-119212742 | Common:4; Rare:119 | ||||
| chr4:119300536-119301003 | Common:2; Rare:187 | ||||
| chr4:119627291-119627398 | Rare:31 | ||||
| chr4:120066769-120066904 | Common:1; Rare:42 | ||||
| chr4:120922813-120922962 | Rare:45; Clinvar:2 | ||||
| chr4:121801233-121801371 | Common:1; Rare:43 |