| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:22899494-22899642 | Common:5; Rare:66 | ||||
| chr22:22900876-22900919 | Common:2; Rare:4 | ||||
| chr22:22900961-22901318 | Common:6; Rare:148 | ||||
| chr22:22906169-22906379 | Rare:60 | ||||
| chr22:22906442-22906465 | Rare:7 | ||||
| chr22:22906467-22906569 | Common:1; Rare:51 | ||||
| chr22:22906642-22906813 | Common:4; Rare:60 | ||||
| chr22:22922694-22922751 | Rare:26 | ||||
| chr22:23152903-23153088 | Rare:50 | ||||
| chr22:23833489-23833614 | Rare:29; Clinvar:2; Clinvar (benign):4 | ||||
| chr22:24243679-24243929 | Common:2; Rare:53 | ||||
| chr22:26657379-26657639 | Common:2; Rare:46 | ||||
| chr22:26672613-26673137 | Common:4; Rare:148 | ||||
| chr22:26705500-26705808 | Common:1; Rare:49 | ||||
| chr22:26708206-26708488 | Common:4; Rare:38 |