| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109009405-109009677 | Common:2; Rare:80 | ||||
| chr6:109094383-109094607 | Rare:53 | ||||
| chr6:109094810-109095210 | Common:5; Rare:122 | ||||
| chr6:109095421-109095551 | Rare:27 | ||||
| chr6:109440569-109440911 | Common:2; Rare:115 | ||||
| chr6:109455640-109455865 | Common:4; Rare:65 | ||||
| chr6:109691034-109691384 | Common:4; Rare:86; Clinvar:5; Clinvar (benign):3 | ||||
| chr6:110179962-110180127 | Common:2; Rare:51 | ||||
| chr6:110415511-110415670 | Rare:37 | ||||
| chr6:110874624-110874796 | Common:4; Rare:59 | ||||
| chr6:110958549-110958772 | Common:4; Rare:77 | ||||
| chr6:110981976-110982100 | Common:2; Rare:63 | ||||
| chr6:111406092-111406368 | Rare:50 | ||||
| chr6:111483136-111483505 | Common:1; Rare:119 | ||||
| chr6:111483644-111483769 | Common:1; Rare:49 |