| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:67062085-67062465 | Rare:96 | ||||
| chr8:67064221-67064475 | Common:3; Rare:108; Clinvar (benign):2 | ||||
| chr8:69833618-69833742 | Rare:17 | ||||
| chr8:69833939-69834161 | Common:2; Rare:50 | ||||
| chr8:69835025-69835107 | Common:2; Rare:12 | ||||
| chr8:70402061-70402271 | Rare:68 | ||||
| chr8:70403771-70403931 | Rare:64 | ||||
| chr8:70608188-70608594 | Common:3; Rare:118 | ||||
| chr8:70669116-70669400 | Common:2; Rare:106 | ||||
| chr8:71356660-71356852 | Rare:40 | ||||
| chr8:71361723-71361842 | Rare:32; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:71361865-71361886 | Rare:1 | ||||
| chr8:71361907-71362031 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:71843801-71844171 | Rare:134 | ||||
| chr8:72537690-72537864 | Common:2; Rare:33 |