| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109009476-109009682 | Common:2; Rare:65 | ||||
| chr6:109382379-109382577 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr6:109455706-109455804 | Common:1; Rare:30 | ||||
| chr6:109455939-109456074 | Rare:20 | ||||
| chr6:109691145-109691332 | Common:3; Rare:46; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179911-110180163 | Common:2; Rare:72 | ||||
| chr6:110874587-110874805 | Common:4; Rare:74 | ||||
| chr6:110959126-110959169 | Common:1; Rare:15 | ||||
| chr6:110981975-110982109 | Common:2; Rare:72 | ||||
| chr6:111483133-111483562 | Common:1; Rare:150 | ||||
| chr6:112087468-112087684 | Rare:62 | ||||
| chr6:112254272-112254756 | Rare:86 | ||||
| chr6:113857213-113857490 | Common:2; Rare:67 | ||||
| chr6:113857494-113857577 | Rare:13 | ||||
| chr6:113857586-113857632 | Common:1; Rare:12 |