| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:41577985-41578256 | Rare:85 | ||||
| chr8:41797613-41797775 | Common:2; Rare:41; Clinvar (pathogenic):2 | ||||
| chr8:42051977-42052266 | Common:1; Rare:84 | ||||
| chr8:42338377-42338525 | Common:1; Rare:63 | ||||
| chr8:42391550-42391925 | Common:4; Rare:114 | ||||
| chr8:42541103-42541188 | Common:1; Rare:18 | ||||
| chr8:42541494-42541741 | Common:2; Rare:75 | ||||
| chr8:42842799-42843014 | Common:2; Rare:66 | ||||
| chr8:42843041-42843128 | Rare:28; Clinvar:3 | ||||
| chr8:42843215-42843527 | Common:3; Rare:86; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:42896289-42896383 | Rare:39 | ||||
| chr8:42896522-42897177 | Common:1; Rare:244 | ||||
| chr8:43056196-43056463 | Rare:106 | ||||
| chr8:43140373-43140597 | Common:2; Rare:80; Clinvar:9 | ||||
| chr8:47260834-47261003 | Common:3; Rare:71 |