| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:30833446-30833710 | Rare:54 | ||||
| chr22:30841410-30841770 | Common:2; Rare:112 | ||||
| chr22:30968984-30969316 | Common:6; Rare:200 | ||||
| chr22:31347350-31347900 | Common:3; Rare:329 | ||||
| chr22:32532420-32532980 | Common:4; Rare:161 | ||||
| chr22:32591694-32591949 | Common:3; Rare:101 | ||||
| chr22:35301610-35301960 | Common:2; Rare:96 | ||||
| chr22:35403264-35403480 | Rare:67 | ||||
| chr22:35406380-35406680 | Common:3; Rare:101 | ||||
| chr22:35408251-35408678 | Rare:234 | ||||
| chr22:35587530-35587764 | Common:2; Rare:78 | ||||
| chr22:35627500-35628057 | Rare:263 | ||||
| chr22:35894994-35895106 | Rare:32 | ||||
| chr22:36028936-36029285 | Common:6; Rare:137 | ||||
| chr22:36348780-36349500 | Common:10; Rare:206; Clinvar:6; Clinvar (benign):10; Clinvar (pathogenic):2 |