| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46635467-46635689 | Common:4; Rare:74 | ||||
| chr22:17159200-17159375 | Common:4; Rare:82 | ||||
| chr22:17219373-17219451 | Common:2; Rare:15 | ||||
| chr22:17594721-17594949 | Common:3; Rare:50 | ||||
| chr22:17628706-17628872 | Common:1; Rare:56 | ||||
| chr22:17638668-17638811 | Rare:49 | ||||
| chr22:17774393-17774569 | Rare:61 | ||||
| chr22:18077820-18078014 | Common:3; Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:19122389-19122667 | Common:3; Rare:65 | ||||
| chr22:19432303-19432607 | Common:4; Rare:130 | ||||
| chr22:19447677-19447878 | Common:2; Rare:83 | ||||
| chr22:19479132-19479471 | Common:4; Rare:120 | ||||
| chr22:19479698-19479977 | Common:4; Rare:77 | ||||
| chr22:19854811-19855033 | Rare:87 | ||||
| chr22:19941715-19941877 | Rare:70; Clinvar:5; Clinvar (benign):4 |