| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:37762478-37762699 | Common:2; Rare:80 | ||||
| chr8:37796366-37796418 | Rare:11 | ||||
| chr8:38030278-38030580 | Common:3; Rare:86 | ||||
| chr8:38105356-38105553 | Common:2; Rare:60 | ||||
| chr8:38105779-38105939 | Rare:47 | ||||
| chr8:38176430-38176557 | Common:1; Rare:46 | ||||
| chr8:38176674-38176883 | Common:4; Rare:59 | ||||
| chr8:38231556-38231772 | Rare:54 | ||||
| chr8:38269167-38269252 | Rare:32 | ||||
| chr8:38901082-38901179 | Common:1; Rare:25 | ||||
| chr8:38996443-38997038 | Common:7; Rare:225 | ||||
| chr8:40153352-40153541 | Common:1; Rare:49 | ||||
| chr8:41797582-41797776 | Common:2; Rare:46; Clinvar (pathogenic):2 | ||||
| chr8:42391697-42391925 | Common:3; Rare:81 | ||||
| chr8:42541039-42541433 | Common:2; Rare:94 |