| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:108260917-108261106 | Rare:88 | ||||
| chr6:109009434-109009682 | Common:2; Rare:77 | ||||
| chr6:109094317-109094587 | Rare:58 | ||||
| chr6:109382348-109382844 | Common:6; Rare:165; Clinvar (benign):1 | ||||
| chr6:109440581-109440856 | Common:1; Rare:91 | ||||
| chr6:109455726-109455835 | Rare:24 | ||||
| chr6:109691158-109691322 | Common:3; Rare:40; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179962-110180170 | Common:2; Rare:62 | ||||
| chr6:110981959-110982100 | Common:2; Rare:68 | ||||
| chr6:111483214-111483537 | Common:1; Rare:115 | ||||
| chr6:112087446-112087684 | Rare:74 | ||||
| chr6:116100709-116100886 | Rare:65 | ||||
| chr6:116254062-116254201 | Common:2; Rare:36 | ||||
| chr6:116279873-116280120 | Common:2; Rare:78 | ||||
| chr6:116571183-116571595 | Common:3; Rare:118 |