| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36252990-36253140 | Rare:29 | ||||
| chr22:36387986-36388276 | Common:2; Rare:84; Clinvar (benign):1 | ||||
| chr22:36529094-36529504 | Common:6; Rare:127 | ||||
| chr22:37199383-37199554 | Common:2; Rare:39 | ||||
| chr22:37608665-37608875 | Common:2; Rare:64 | ||||
| chr22:37675969-37676188 | Rare:35 | ||||
| chr22:37805566-37805868 | Rare:92 | ||||
| chr22:37807767-37807958 | Common:4; Rare:64 | ||||
| chr22:37849297-37849480 | Rare:109 | ||||
| chr22:37953550-37953745 | Rare:78 | ||||
| chr22:38181734-38181984 | Common:3; Rare:66; Clinvar:1 | ||||
| chr22:38505980-38506215 | Common:1; Rare:83 | ||||
| chr22:38570155-38570500 | Common:5; Rare:65 | ||||
| chr22:38656357-38656706 | Common:1; Rare:90 | ||||
| chr22:38681817-38681991 | Common:1; Rare:72 |