| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:100881193-100881485 | Common:6; Rare:105 | ||||
| chr6:105137105-105137276 | Common:1; Rare:65 | ||||
| chr6:106629454-106629620 | Common:1; Rare:35 | ||||
| chr6:107957255-107957424 | Rare:35 | ||||
| chr6:109094818-109095153 | Common:3; Rare:94 | ||||
| chr6:109382392-109382567 | Common:4; Rare:71; Clinvar (benign):1 | ||||
| chr6:109440604-109440914 | Common:2; Rare:103 | ||||
| chr6:109691135-109691329 | Common:3; Rare:49; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179896-110180122 | Common:2; Rare:64 | ||||
| chr6:110981979-110982097 | Common:2; Rare:58 | ||||
| chr6:111483121-111483602 | Common:1; Rare:173 | ||||
| chr6:112087463-112087688 | Rare:63 | ||||
| chr6:113970983-113971495 | Common:4; Rare:181 | ||||
| chr6:116100703-116100886 | Rare:67 | ||||
| chr6:116254045-116254224 | Common:5; Rare:50 |