| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:35840366-35840545 | Rare:33 | ||||
| chr22:36296981-36297071 | Rare:31; Clinvar (benign):1 | ||||
| chr22:36481548-36481651 | Common:1; Rare:37 | ||||
| chr22:36507031-36507147 | Common:2; Rare:39 | ||||
| chr22:36529075-36529542 | Common:6; Rare:148 | ||||
| chr22:37019403-37019803 | Common:5; Rare:114 | ||||
| chr22:37560324-37560556 | Common:1; Rare:77 | ||||
| chr22:37608808-37609059 | Common:2; Rare:77 | ||||
| chr22:37849316-37849480 | Rare:93 | ||||
| chr22:37953609-37953755 | Rare:63 | ||||
| chr22:38181798-38182024 | Common:2; Rare:58 | ||||
| chr22:38505980-38506016 | Rare:9 | ||||
| chr22:38506285-38506619 | Common:1; Rare:105 | ||||
| chr22:38570155-38570493 | Common:5; Rare:64 | ||||
| chr22:38656391-38656706 | Common:1; Rare:70 |