| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17774400-17774593 | Rare:65 | ||||
| chr22:18001106-18001247 | Common:3; Rare:40 | ||||
| chr22:18001398-18001945 | Common:10; Rare:268 | ||||
| chr22:18023730-18025001 | Common:11; Rare:300 | ||||
| chr22:18077741-18078096 | Common:17; Rare:293; Clinvar:9; Clinvar (benign):9 | ||||
| chr22:18078439-18078810 | Common:3; Rare:259; Clinvar:30; Clinvar (benign):6 | ||||
| chr22:18110240-18110365 | Common:1; Rare:14 | ||||
| chr22:18110304-18110746 | Common:1; Rare:131 | ||||
| chr22:18149570-18150070 | Common:4; Rare:203 | ||||
| chr22:19121400-19122040 | Common:3; Rare:324 | ||||
| chr22:19122304-19122752 | Common:15; Rare:295 | ||||
| chr22:19143950-19144260 | Common:2; Rare:86 | ||||
| chr22:19144566-19144787 | Common:2; Rare:96 | ||||
| chr22:19178249-19179092 | Common:18; Rare:688; Clinvar (benign):14 | ||||
| chr22:19291654-19291977 | Common:33; Rare:290 |