| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:99013156-99013355 | Rare:42; Clinvar:1 | ||||
| chr8:99013742-99013886 | Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:99893634-99893796 | Common:2; Rare:64 | ||||
| chr8:100150514-100150699 | Common:1; Rare:68 | ||||
| chr8:100157790-100158190 | Common:2; Rare:80 | ||||
| chr8:100158442-100158603 | Common:1; Rare:28 | ||||
| chr8:100212840-100213330 | Common:7; Rare:149; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr8:100309904-100310296 | Common:1; Rare:142 | ||||
| chr8:100559690-100559902 | Common:1; Rare:55 | ||||
| chr8:100720665-100721421 | Common:10; Rare:384 | ||||
| chr8:100722078-100722352 | Common:1; Rare:98 | ||||
| chr8:100950536-100950706 | Common:8; Rare:92 | ||||
| chr8:100951960-100952301 | Common:1; Rare:131 | ||||
| chr8:100952415-100952675 | Common:1; Rare:83 | ||||
| chr8:100952845-100953122 | Common:4; Rare:84 |