| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:37762487-37762678 | Common:2; Rare:71 | ||||
| chr8:37899477-37899776 | Common:3; Rare:113 | ||||
| chr8:38105356-38105556 | Common:2; Rare:61 | ||||
| chr8:38105773-38105960 | Rare:53 | ||||
| chr8:38150732-38151112 | Common:1; Rare:108; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr8:38176430-38176564 | Common:1; Rare:49 | ||||
| chr8:38176657-38176881 | Common:4; Rare:61 | ||||
| chr8:38231518-38231776 | Rare:73 | ||||
| chr8:38269110-38269469 | Rare:120 | ||||
| chr8:38728288-38728669 | Common:2; Rare:73 | ||||
| chr8:38901057-38901442 | Common:3; Rare:94 | ||||
| chr8:38901700-38902011 | Common:3; Rare:54 | ||||
| chr8:38996220-38996288 | Rare:32 | ||||
| chr8:38996428-38997073 | Common:7; Rare:243 | ||||
| chr8:41490360-41490664 | Common:1; Rare:77 |