| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17199458-17199689 | Common:1; Rare:64 | ||||
| chr22:17368739-17368898 | Rare:43 | ||||
| chr22:17369030-17369131 | Common:1; Rare:29 | ||||
| chr22:17369282-17369499 | Common:1; Rare:99 | ||||
| chr22:17628735-17628979 | Common:1; Rare:78 | ||||
| chr22:17638592-17638832 | Rare:84 | ||||
| chr22:17773886-17774109 | Common:1; Rare:57 | ||||
| chr22:18001671-18001906 | Common:4; Rare:54 | ||||
| chr22:18077795-18078028 | Common:5; Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18078159-18078559 | Rare:225; Clinvar:22; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr22:19122388-19122732 | Common:3; Rare:87 | ||||
| chr22:19144627-19144916 | Common:5; Rare:104 | ||||
| chr22:19178697-19179050 | Common:4; Rare:129; Clinvar (benign):1 | ||||
| chr22:19291630-19292120 | Common:15; Rare:155 | ||||
| chr22:19431680-19431874 | Rare:45 |