| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:30653850-30653984 | Common:3; Rare:18 | ||||
| chr22:30661195-30661405 | Common:1; Rare:32 | ||||
| chr22:30937585-30937875 | Common:1; Rare:77; Clinvar:3 | ||||
| chr22:30937939-30938168 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:30961292-30961368 | Rare:13 | ||||
| chr22:30968978-30969534 | Common:3; Rare:136 | ||||
| chr22:30969788-30969930 | Common:1; Rare:40 | ||||
| chr22:30969969-30970280 | Common:1; Rare:74 | ||||
| chr22:30970282-30970535 | Common:2; Rare:52 | ||||
| chr22:30972230-30972474 | Common:1; Rare:50 | ||||
| chr22:31091422-31091740 | Common:4; Rare:95 | ||||
| chr22:31098706-31099117 | Common:2; Rare:135 | ||||
| chr22:31177963-31178087 | Rare:22 | ||||
| chr22:31185000-31185031 | Rare:4 | ||||
| chr22:31483112-31483202 | Rare:16 |