| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17628698-17628848 | Common:1; Rare:49 | ||||
| chr22:17638689-17638827 | Rare:50 | ||||
| chr22:18077814-18078038 | Common:4; Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18149763-18149991 | Common:1; Rare:38 | ||||
| chr22:19178437-19178533 | Common:1; Rare:28 | ||||
| chr22:19291684-19291924 | Common:10; Rare:77 | ||||
| chr22:19432296-19432606 | Common:4; Rare:134 | ||||
| chr22:19447513-19447836 | Common:2; Rare:148 | ||||
| chr22:19479084-19479466 | Common:4; Rare:138 | ||||
| chr22:19524398-19524715 | Common:2; Rare:90 | ||||
| chr22:19854791-19854997 | Rare:71 | ||||
| chr22:19941712-19941888 | Rare:75; Clinvar:6; Clinvar (benign):4 | ||||
| chr22:19963102-19963271 | Common:1; Rare:44 | ||||
| chr22:19963886-19964183 | Rare:71 | ||||
| chr22:20079921-20080302 | Common:1; Rare:125 |