| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36462122-36462553 | Common:15; Rare:268 | ||||
| chr22:36465321-36465760 | Common:4; Rare:204 | ||||
| chr22:36465780-36466110 | Common:2; Rare:83 | ||||
| chr22:36569990-36570380 | Common:5; Rare:93 | ||||
| chr22:36648060-36648540 | Rare:83 | ||||
| chr22:36659690-36660130 | Common:2; Rare:160 | ||||
| chr22:36660168-36660490 | Common:2; Rare:64 | ||||
| chr22:36806230-36806760 | Common:4; Rare:108 | ||||
| chr22:36808700-36809170 | Common:2; Rare:82 | ||||
| chr22:36870230-36870840 | Common:9; Rare:259; Clinvar:10; Clinvar (benign):4 | ||||
| chr22:37032040-37032522 | Common:2; Rare:132 | ||||
| chr22:37032767-37033469 | Common:6; Rare:271 | ||||
| chr22:37063465-37063714 | Common:2; Rare:52 | ||||
| chr22:37178826-37179235 | Common:6; Rare:170 | ||||
| chr22:37183380-37183800 | Common:3; Rare:78 |