| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:32780419-32780691 | Common:4; Rare:80 | ||||
| chr22:32810251-32810646 | Common:3; Rare:77 | ||||
| chr22:33335712-33336251 | Common:17; Rare:250 | ||||
| chr22:33539750-33540680 | Common:16; Rare:283 | ||||
| chr22:33573660-33573824 | Common:2; Rare:52 | ||||
| chr22:33920983-33921269 | Common:2; Rare:225 | ||||
| chr22:35301560-35301960 | Common:3; Rare:138 | ||||
| chr22:35328505-35328905 | Common:9; Rare:138 | ||||
| chr22:35403441-35403665 | Common:2; Rare:55 | ||||
| chr22:35406495-35407050 | Common:9; Rare:233 | ||||
| chr22:35412122-35412610 | Common:4; Rare:260 | ||||
| chr22:36251870-36252260 | Common:4; Rare:129 | ||||
| chr22:36348619-36349470 | Common:12; Rare:348; Clinvar:10; Clinvar (benign):18; Clinvar (pathogenic):2 | ||||
| chr22:36352010-36352360 | Common:6; Rare:129 | ||||
| chr22:36352720-36353130 | Common:15; Rare:100 |