| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:73063202-73063324 | Common:3; Rare:17 | ||||
| chr8:73064080-73064287 | Common:3; Rare:34 | ||||
| chr8:73064403-73064731 | Common:2; Rare:43 | ||||
| chr8:81281405-81281507 | Common:1; Rare:16 | ||||
| chr8:86344731-86344954 | Common:2; Rare:37 | ||||
| chr8:86462179-86462348 | Common:1; Rare:30 | ||||
| chr8:86466652-86466741 | Rare:18 | ||||
| chr8:86471559-86471826 | Rare:57 | ||||
| chr8:86476103-86476136 | Rare:4 | ||||
| chr8:89964443-89964717 | Common:3; Rare:67; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr8:92083918-92084072 | Rare:21 | ||||
| chr8:92101584-92101963 | Common:2; Rare:75 | ||||
| chr8:92102088-92102364 | Common:1; Rare:53 | ||||
| chr8:98032982-98033089 | Rare:18 | ||||
| chr8:98699241-98699319 | Common:1; Rare:13 |