| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42541565-42541666 | Rare:34 | ||||
| chr8:42541691-42541933 | Common:1; Rare:79; Clinvar (benign):1 | ||||
| chr8:42843045-42843092 | Rare:11; Clinvar:2 | ||||
| chr8:42843283-42843523 | Common:2; Rare:68; Clinvar (benign):3 | ||||
| chr8:42896613-42897037 | Common:1; Rare:171 | ||||
| chr8:43056185-43056463 | Common:1; Rare:110 | ||||
| chr8:47260803-47260982 | Common:3; Rare:75 | ||||
| chr8:47960106-47960212 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:47960693-47960974 | Common:2; Rare:104; Clinvar:9; Clinvar (benign):1 | ||||
| chr8:48008348-48008457 | Common:2; Rare:67 | ||||
| chr8:51898981-51899347 | Common:7; Rare:163 | ||||
| chr8:52714427-52714571 | Common:1; Rare:60 | ||||
| chr8:53843230-53843370 | Rare:33 | ||||
| chr8:54021921-54022052 | Rare:64 | ||||
| chr8:54022209-54022543 | Common:1; Rare:109 |