| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42614930-42615244 | Common:3; Rare:126 | ||||
| chr22:42649328-42649482 | Common:1; Rare:61 | ||||
| chr22:42857172-42857430 | Common:3; Rare:108 | ||||
| chr22:43955348-43955556 | Common:2; Rare:60 | ||||
| chr22:45163786-45164003 | Common:2; Rare:80 | ||||
| chr22:46053794-46053863 | Rare:26 | ||||
| chr22:46250276-46250408 | Common:1; Rare:42 | ||||
| chr22:46296711-46296924 | Common:2; Rare:77 | ||||
| chr22:46335621-46335760 | Common:2; Rare:57; Clinvar:4; Clinvar (benign):6 | ||||
| chr22:46762506-46762669 | Common:3; Rare:58 | ||||
| chr22:50244986-50245114 | Common:1; Rare:52 | ||||
| chr22:50582800-50583150 | Common:6; Rare:117; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:50783611-50783859 | Common:2; Rare:74 | ||||
| chr3:3126784-3126984 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr3:4467229-4467350 | Rare:47; Clinvar:1; Clinvar (benign):1 |