| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:30606993-30607321 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):3 | ||||
| chr22:31081128-31081345 | Common:1; Rare:56 | ||||
| chr22:31107422-31107759 | Common:2; Rare:105 | ||||
| chr22:31290718-31290906 | Rare:76 | ||||
| chr22:31292419-31292519 | Rare:24 | ||||
| chr22:31489784-31490164 | Common:3; Rare:153 | ||||
| chr22:31630829-31631037 | Common:4; Rare:50 | ||||
| chr22:31750037-31750330 | Common:3; Rare:84 | ||||
| chr22:31753805-31754028 | Common:1; Rare:80 | ||||
| chr22:35299733-35299979 | Common:2; Rare:66 | ||||
| chr22:35615574-35615798 | Common:4; Rare:43 | ||||
| chr22:35617076-35617523 | Rare:107 | ||||
| chr22:36529078-36529519 | Common:6; Rare:138 | ||||
| chr22:37019402-37019784 | Common:5; Rare:109 | ||||
| chr22:37560331-37560516 | Common:1; Rare:64 |