| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46150320-46150646 | Common:1; Rare:107 | ||||
| chr22:46250254-46250408 | Common:2; Rare:47 | ||||
| chr22:46267826-46268041 | Common:1; Rare:66 | ||||
| chr22:46296601-46297030 | Common:4; Rare:131 | ||||
| chr22:46335601-46335819 | Common:5; Rare:103; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762458-46762669 | Common:3; Rare:78 | ||||
| chr22:50185725-50185953 | Common:4; Rare:95 | ||||
| chr22:50244960-50245080 | Common:2; Rare:48 | ||||
| chr22:50525531-50525712 | Common:4; Rare:88; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50578381-50578717 | Common:1; Rare:89 | ||||
| chr22:50582370-50582440 | Rare:33 | ||||
| chr22:50582784-50583136 | Common:7; Rare:114; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628059-50628289 | Common:9; Rare:106; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783616-50783882 | Common:2; Rare:80 | ||||
| chr3:2098643-2098962 | Common:4; Rare:126 |