| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:100881245-100881482 | Common:5; Rare:92 | ||||
| chr6:106325547-106325896 | Common:1; Rare:114 | ||||
| chr6:106629462-106629661 | Common:3; Rare:47 | ||||
| chr6:107459537-107459703 | Common:1; Rare:38 | ||||
| chr6:108294787-108295079 | Common:1; Rare:79 | ||||
| chr6:108560726-108560984 | Rare:107 | ||||
| chr6:108848190-108848456 | Common:1; Rare:86 | ||||
| chr6:109095407-109095557 | Rare:33 | ||||
| chr6:109382066-109382231 | Common:4; Rare:66 | ||||
| chr6:109382348-109382827 | Common:6; Rare:161; Clinvar (benign):1 | ||||
| chr6:109440575-109440842 | Common:1; Rare:91 | ||||
| chr6:109455726-109455854 | Common:1; Rare:32 | ||||
| chr6:109483179-109483218 | Rare:19 | ||||
| chr6:109691145-109691329 | Common:3; Rare:46; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110958435-110958545 | Common:2; Rare:31 |