| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17159190-17159393 | Common:5; Rare:101 | ||||
| chr22:17628675-17628866 | Common:1; Rare:68 | ||||
| chr22:17638647-17638851 | Rare:78 | ||||
| chr22:18077814-18078058 | Common:4; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19122389-19122652 | Common:3; Rare:60 | ||||
| chr22:19178449-19178527 | Common:1; Rare:19 | ||||
| chr22:19291656-19291992 | Common:12; Rare:124 | ||||
| chr22:19432296-19432614 | Common:4; Rare:136 | ||||
| chr22:19447678-19447963 | Common:2; Rare:115 | ||||
| chr22:19479698-19479960 | Common:4; Rare:72 | ||||
| chr22:19719053-19719147 | Rare:33 | ||||
| chr22:19854806-19854972 | Rare:58 | ||||
| chr22:19941773-19941891 | Rare:50; Clinvar:2 | ||||
| chr22:20016686-20017002 | Common:6; Rare:107 | ||||
| chr22:20020897-20021151 | Common:1; Rare:86 |