| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42553714-42554023 | Common:1; Rare:102 | ||||
| chr22:42614853-42615251 | Common:3; Rare:166 | ||||
| chr22:42649322-42649483 | Common:1; Rare:65 | ||||
| chr22:43015104-43015384 | Common:2; Rare:116 | ||||
| chr22:43089325-43089480 | Common:3; Rare:53 | ||||
| chr22:43110563-43110778 | Common:3; Rare:58 | ||||
| chr22:43151469-43151582 | Common:1; Rare:27 | ||||
| chr22:43812292-43812448 | Common:2; Rare:56 | ||||
| chr22:43955289-43955562 | Common:3; Rare:81 | ||||
| chr22:45163674-45164008 | Common:4; Rare:121 | ||||
| chr22:45309722-45309975 | Common:1; Rare:99 | ||||
| chr22:45671744-45672066 | Common:3; Rare:115 | ||||
| chr22:46250236-46250423 | Common:3; Rare:58 | ||||
| chr22:46296584-46296924 | Common:2; Rare:105 | ||||
| chr22:46335621-46335776 | Common:4; Rare:66; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 |