| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:73878820-73879045 | Common:3; Rare:109 | ||||
| chr8:73970909-73971009 | Common:1; Rare:11 | ||||
| chr8:73972009-73972449 | Common:2; Rare:126 | ||||
| chr8:73976064-73976488 | Common:6; Rare:155; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:74350281-74350459 | Common:2; Rare:74; Clinvar (benign):2 | ||||
| chr8:77000051-77000312 | Common:1; Rare:89; Clinvar:5 | ||||
| chr8:80029911-80030021 | Common:1; Rare:45 | ||||
| chr8:80030037-80030098 | Rare:34 | ||||
| chr8:80171440-80171744 | Common:5; Rare:84 | ||||
| chr8:80485896-80486285 | Rare:100 | ||||
| chr8:81721264-81721425 | Rare:65 | ||||
| chr8:81732351-81732552 | Common:2; Rare:46 | ||||
| chr8:81842178-81842440 | Common:15; Rare:32 | ||||
| chr8:85177040-85177221 | Common:3; Rare:48 | ||||
| chr8:85220304-85220508 | Rare:70 |