| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41947089-41947225 | Rare:50 | ||||
| chr22:41998656-41998811 | Common:1; Rare:53 | ||||
| chr22:42070646-42071049 | Common:4; Rare:96 | ||||
| chr22:42079614-42079763 | Common:1; Rare:48 | ||||
| chr22:42090658-42091060 | Common:2; Rare:164; Clinvar (pathogenic):1 | ||||
| chr22:42519746-42519893 | Common:1; Rare:66 | ||||
| chr22:42614815-42615256 | Common:3; Rare:199 | ||||
| chr22:42649311-42649482 | Common:1; Rare:67 | ||||
| chr22:42857151-42857450 | Common:3; Rare:120 | ||||
| chr22:42946643-42946749 | Common:1; Rare:19 | ||||
| chr22:42947069-42947521 | Common:4; Rare:79 | ||||
| chr22:42959763-42959999 | Common:1; Rare:41 | ||||
| chr22:42960255-42960367 | Common:1; Rare:16 | ||||
| chr22:43015087-43015387 | Common:2; Rare:124 | ||||
| chr22:43089325-43089507 | Common:3; Rare:58 |