| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38105775-38105931 | Rare:46 | ||||
| chr8:38176365-38176564 | Common:1; Rare:73 | ||||
| chr8:38176650-38176890 | Common:5; Rare:66 | ||||
| chr8:38231701-38231858 | Rare:34 | ||||
| chr8:38901208-38901352 | Rare:28 | ||||
| chr8:38996443-38997155 | Common:8; Rare:268; Clinvar (benign):1 | ||||
| chr8:41309126-41309141 | Rare:7 | ||||
| chr8:42271247-42271442 | Common:1; Rare:67 | ||||
| chr8:42541135-42541175 | Rare:9 | ||||
| chr8:42541549-42541783 | Rare:82 | ||||
| chr8:42541907-42542045 | Rare:38; Clinvar:3 | ||||
| chr8:42843079-42843092 | Rare:1 | ||||
| chr8:42896274-42897173 | Common:3; Rare:375 | ||||
| chr8:42897275-42897379 | Rare:30 | ||||
| chr8:43056153-43056457 | Common:1; Rare:117 |