| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:109801919-109802249 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chr4:109815458-109815762 | Common:1; Rare:82 | ||||
| chr4:110475953-110476287 | Common:1; Rare:62 | ||||
| chr4:112231591-112231852 | Common:2; Rare:80 | ||||
| chr4:112285789-112285987 | Rare:61 | ||||
| chr4:112636880-112637187 | Common:1; Rare:85 | ||||
| chr4:112637364-112637570 | Common:3; Rare:56 | ||||
| chr4:113761123-113761231 | Rare:26 | ||||
| chr4:113979582-113979837 | Common:6; Rare:60 | ||||
| chr4:118685347-118685450 | Common:2; Rare:35 | ||||
| chr4:118835946-118836224 | Common:1; Rare:64 | ||||
| chr4:119212406-119212730 | Common:2; Rare:98 | ||||
| chr4:119300502-119301087 | Common:2; Rare:218 | ||||
| chr4:120066754-120066955 | Common:3; Rare:62 | ||||
| chr4:121696862-121697133 | Common:5; Rare:74 |