| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38176398-38176864 | Common:5; Rare:137 | ||||
| chr8:38269115-38269288 | Rare:69 | ||||
| chr8:38382161-38382440 | Common:2; Rare:89 | ||||
| chr8:38386321-38386518 | Common:1; Rare:42 | ||||
| chr8:38757161-38757303 | Common:2; Rare:30 | ||||
| chr8:38787005-38787242 | Rare:90 | ||||
| chr8:38996475-38996793 | Common:2; Rare:99 | ||||
| chr8:41578007-41578213 | Rare:58 | ||||
| chr8:41797509-41797808 | Common:2; Rare:86; Clinvar (pathogenic):2 | ||||
| chr8:42051976-42052272 | Common:1; Rare:86 | ||||
| chr8:42338377-42338525 | Common:1; Rare:63 | ||||
| chr8:42391695-42391912 | Common:3; Rare:76 | ||||
| chr8:42541562-42541854 | Rare:107 | ||||
| chr8:42843046-42843116 | Rare:20; Clinvar:3 | ||||
| chr8:42843227-42843514 | Common:2; Rare:84; Clinvar:1; Clinvar (benign):3 |