| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:96521679-96521887 | Common:7; Rare:101 | ||||
| chr6:96897725-96898044 | Common:4; Rare:118; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:99424668-99424926 | Rare:65 | ||||
| chr6:99425214-99425442 | Common:2; Rare:68 | ||||
| chr6:99425657-99425770 | Rare:26 | ||||
| chr6:99515400-99515602 | Common:1; Rare:65 | ||||
| chr6:100881179-100881501 | Common:6; Rare:117 | ||||
| chr6:105137059-105137299 | Common:1; Rare:87 | ||||
| chr6:106325551-106325859 | Common:1; Rare:99 | ||||
| chr6:106629462-106629645 | Common:3; Rare:42 | ||||
| chr6:107459528-107459700 | Common:1; Rare:38 | ||||
| chr6:107490451-107490589 | Common:2; Rare:49 | ||||
| chr6:108074647-108074928 | Common:1; Rare:101; Clinvar:1 | ||||
| chr6:108260766-108261028 | Rare:116 | ||||
| chr6:108294828-108295076 | Common:1; Rare:68 |