| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46635351-46635694 | Common:8; Rare:125 | ||||
| chr22:17199582-17199686 | Common:1; Rare:31 | ||||
| chr22:17628706-17628890 | Common:1; Rare:66 | ||||
| chr22:17638653-17638819 | Rare:58 | ||||
| chr22:18077820-18078014 | Common:3; Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:19178497-19178517 | Rare:3 | ||||
| chr22:19447667-19447967 | Common:2; Rare:124 | ||||
| chr22:19479125-19479247 | Common:2; Rare:58 | ||||
| chr22:19479687-19479949 | Common:4; Rare:66 | ||||
| chr22:19854811-19855013 | Rare:77 | ||||
| chr22:20117181-20117606 | Common:3; Rare:136 | ||||
| chr22:20319998-20320159 | Common:1; Rare:54 | ||||
| chr22:20393950-20394194 | Common:1; Rare:75 | ||||
| chr22:20495771-20495925 | Common:2; Rare:56 | ||||
| chr22:20982196-20982347 | Common:2; Rare:34; Clinvar (benign):2; Clinvar (pathogenic):1 |