| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:108074661-108074919 | Common:1; Rare:89; Clinvar:1 | ||||
| chr6:108260764-108260815 | Rare:14 | ||||
| chr6:108294806-108295082 | Common:1; Rare:74 | ||||
| chr6:108560726-108560963 | Rare:100 | ||||
| chr6:109009396-109009689 | Common:2; Rare:86 | ||||
| chr6:109094392-109094571 | Rare:43 | ||||
| chr6:109095434-109095551 | Rare:24 | ||||
| chr6:109382374-109382829 | Common:6; Rare:149; Clinvar (benign):1 | ||||
| chr6:109440571-109440872 | Common:2; Rare:108 | ||||
| chr6:109691161-109691339 | Common:3; Rare:42; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179934-110180160 | Common:2; Rare:66 | ||||
| chr6:110958603-110958772 | Common:3; Rare:61 | ||||
| chr6:110981975-110982100 | Common:2; Rare:64 | ||||
| chr6:111483145-111483537 | Common:1; Rare:136 | ||||
| chr6:111483616-111483775 | Common:1; Rare:61 |