| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:23752875-23752942 | Rare:31 | ||||
| chr22:23800386-23800597 | Common:1; Rare:51 | ||||
| chr22:23801056-23801205 | Common:1; Rare:48; Clinvar:5 | ||||
| chr22:23803151-23803339 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:23847915-23848108 | Common:4; Rare:40 | ||||
| chr22:23895467-23895641 | Common:2; Rare:49 | ||||
| chr22:23913421-23913586 | Common:1; Rare:29 | ||||
| chr22:23913885-23914253 | Common:5; Rare:139 | ||||
| chr22:24146352-24146597 | Common:1; Rare:46 | ||||
| chr22:24157794-24157946 | Rare:25 | ||||
| chr22:24242810-24243048 | Common:2; Rare:55 | ||||
| chr22:24243345-24243372 | Rare:7 | ||||
| chr22:24400677-24401088 | Common:1; Rare:62 | ||||
| chr22:24429253-24429402 | Rare:28 | ||||
| chr22:24434158-24434390 | Rare:45 |