| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166382860-166383189 | Common:3; Rare:115 | ||||
| chr6:166627944-166628257 | Common:1; Rare:69 | ||||
| chr6:166956165-166956367 | Common:1; Rare:48; Clinvar:8; Clinvar (benign):1 | ||||
| chr6:166956501-166956725 | Common:6; Rare:78; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:166999129-166999472 | Common:2; Rare:118 | ||||
| chr6:166999889-166999969 | Common:1; Rare:29 | ||||
| chr6:167826377-167826558 | Common:4; Rare:60 | ||||
| chr6:167826731-167827191 | Common:2; Rare:242 | ||||
| chr6:167932547-167932650 | Common:2; Rare:16 | ||||
| chr6:169701951-169702347 | Common:5; Rare:168 | ||||
| chr6:169751480-169751648 | Common:1; Rare:73; Clinvar (benign):2 | ||||
| chr6:170306548-170306808 | Common:1; Rare:87 | ||||
| chr6:170554211-170554452 | Common:2; Rare:75 | ||||
| chr7:519120-519294 | Rare:47 | ||||
| chr7:727214-727308 | Rare:32; Clinvar:2 |