| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:108294802-108295159 | Common:2; Rare:120 | ||||
| chr6:108560730-108560866 | Rare:61 | ||||
| chr6:108848332-108848508 | Rare:63 | ||||
| chr6:108848650-108848813 | Rare:40 | ||||
| chr6:109009432-109009689 | Common:2; Rare:80 | ||||
| chr6:109094317-109094535 | Rare:48 | ||||
| chr6:109094790-109095197 | Common:5; Rare:120 | ||||
| chr6:109095421-109095557 | Rare:28 | ||||
| chr6:109382075-109382196 | Common:4; Rare:52 | ||||
| chr6:109382239-109382358 | Rare:49; Clinvar (benign):1 | ||||
| chr6:109382365-109382838 | Common:6; Rare:157; Clinvar (benign):1 | ||||
| chr6:109440552-109440863 | Common:1; Rare:116 | ||||
| chr6:109691145-109691329 | Common:3; Rare:46; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110415502-110415670 | Rare:41 | ||||
| chr6:110815850-110815996 | Common:1; Rare:42 |