| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19717742-19718651 | Common:16; Rare:822 | ||||
| chr22:19718960-19719430 | Rare:192 | ||||
| chr22:19722279-19722472 | Common:1; Rare:72 | ||||
| chr22:19722407-19722825 | Common:9; Rare:268 | ||||
| chr22:19723260-19724342 | Common:12; Rare:775; Clinvar (benign):1; Clinvar (pathogenic):6 | ||||
| chr22:19756451-19757209 | Common:7; Rare:545 | ||||
| chr22:19760410-19760903 | Common:5; Rare:384 | ||||
| chr22:19760895-19761580 | Common:4; Rare:241; Clinvar:5; Clinvar (benign):7 | ||||
| chr22:19765113-19765590 | Common:6; Rare:197; Clinvar:1 | ||||
| chr22:19854301-19854701 | Rare:116 | ||||
| chr22:19854653-19855198 | Common:30; Rare:1346 | ||||
| chr22:19855199-19855599 | Common:2; Rare:90 | ||||
| chr22:19918690-19919090 | Common:6; Rare:126; Clinvar:4; Clinvar (benign):5 | ||||
| chr22:19941084-19942743 | Common:37; Rare:1145; Clinvar:34; Clinvar (benign):28 | ||||
| chr22:19961835-19963654 | Common:19; Rare:815; Clinvar:2; Clinvar (benign):2 |