| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:108560726-108560984 | Rare:107 | ||||
| chr6:108848294-108848482 | Rare:69 | ||||
| chr6:109009405-109009682 | Common:2; Rare:81 | ||||
| chr6:109094366-109094571 | Rare:49 | ||||
| chr6:109094809-109095153 | Common:3; Rare:97 | ||||
| chr6:109095415-109095557 | Rare:30 | ||||
| chr6:109382066-109382299 | Common:4; Rare:96 | ||||
| chr6:109382304-109382358 | Rare:20; Clinvar (benign):1 | ||||
| chr6:109382365-109382798 | Common:5; Rare:147; Clinvar (benign):1 | ||||
| chr6:109440541-109440880 | Common:2; Rare:124 | ||||
| chr6:109483140-109483274 | Rare:57 | ||||
| chr6:109691145-109691339 | Common:3; Rare:48; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179947-110180162 | Common:2; Rare:62 | ||||
| chr6:110415549-110415693 | Rare:31 | ||||
| chr6:110874616-110874794 | Common:4; Rare:61 |