| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38996481-38996826 | Common:2; Rare:105 | ||||
| chr8:38996903-38997124 | Common:2; Rare:104 | ||||
| chr8:40153341-40153602 | Common:2; Rare:75 | ||||
| chr8:41797561-41797776 | Common:2; Rare:58; Clinvar (pathogenic):2 | ||||
| chr8:42338385-42338509 | Common:1; Rare:52 | ||||
| chr8:42540918-42541189 | Common:1; Rare:69 | ||||
| chr8:42541494-42541661 | Common:2; Rare:45 | ||||
| chr8:42541675-42541741 | Rare:21 | ||||
| chr8:42843277-42843511 | Common:2; Rare:67; Clinvar (benign):3 | ||||
| chr8:42896292-42896382 | Rare:38 | ||||
| chr8:42896591-42896939 | Common:1; Rare:153 | ||||
| chr8:43056210-43056454 | Rare:98 | ||||
| chr8:47260781-47260989 | Common:3; Rare:92 | ||||
| chr8:47960106-47960215 | Common:1; Rare:38; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:47960799-47960990 | Common:1; Rare:71; Clinvar:6 |