| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38105441-38105556 | Common:1; Rare:42 | ||||
| chr8:38105719-38105954 | Common:1; Rare:74 | ||||
| chr8:38176389-38176869 | Common:5; Rare:141 | ||||
| chr8:38269125-38269256 | Rare:51 | ||||
| chr8:38996457-38997061 | Common:7; Rare:225 | ||||
| chr8:41578007-41578256 | Rare:80 | ||||
| chr8:42051976-42052263 | Common:1; Rare:84 | ||||
| chr8:42541102-42541178 | Rare:17 | ||||
| chr8:42541565-42541661 | Rare:32 | ||||
| chr8:42541680-42542070 | Common:1; Rare:119; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:42843045-42843092 | Rare:11; Clinvar:2 | ||||
| chr8:42843268-42843520 | Common:2; Rare:73; Clinvar (benign):3 | ||||
| chr8:42896596-42897027 | Common:1; Rare:175 | ||||
| chr8:43056105-43056463 | Common:1; Rare:127 | ||||
| chr8:47260796-47260977 | Common:3; Rare:78 |