| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88823148-88823367 | Common:2; Rare:35 | ||||
| chr4:88823728-88823809 | Rare:18 | ||||
| chr4:89057075-89057310 | Common:3; Rare:55 | ||||
| chr4:89111097-89111171 | Rare:16 | ||||
| chr4:89111292-89111644 | Common:4; Rare:126 | ||||
| chr4:89837098-89837292 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:95548819-95549334 | Common:3; Rare:140 | ||||
| chr4:98143450-98143638 | Common:1; Rare:48 | ||||
| chr4:98261194-98261505 | Common:1; Rare:98 | ||||
| chr4:98929108-98929366 | Common:3; Rare:64 | ||||
| chr4:98995517-98995774 | Common:5; Rare:86 | ||||
| chr4:99088696-99088900 | Common:7; Rare:93 | ||||
| chr4:99321317-99321509 | Rare:46 | ||||
| chr4:99352961-99353168 | Common:2; Rare:46 | ||||
| chr4:99563606-99563822 | Common:2; Rare:67 |