| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17639002-17639402 | Common:3; Rare:160 | ||||
| chr22:17773195-17774280 | Common:11; Rare:519 | ||||
| chr22:17774380-17774830 | Rare:287 | ||||
| chr22:18001034-18001434 | Common:7; Rare:162 | ||||
| chr22:18001404-18001960 | Common:15; Rare:356 | ||||
| chr22:18077567-18078265 | Common:28; Rare:666; Clinvar:19; Clinvar (benign):14 | ||||
| chr22:18078490-18078960 | Common:7; Rare:213; Clinvar:8; Clinvar (benign):2 | ||||
| chr22:18149517-18150289 | Common:9; Rare:453 | ||||
| chr22:19121633-19122077 | Common:5; Rare:270 | ||||
| chr22:19122264-19122850 | Common:36; Rare:777 | ||||
| chr22:19143880-19144980 | Common:31; Rare:889 | ||||
| chr22:19177597-19178231 | Common:3; Rare:213; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:19178178-19178339 | Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:19178357-19178680 | Common:8; Rare:284; Clinvar (benign):3 | ||||
| chr22:19178600-19179170 | Common:25; Rare:842; Clinvar (benign):9 |