| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46296655-46296977 | Common:2; Rare:111 | ||||
| chr22:46335621-46335933 | Common:8; Rare:144; Clinvar:9; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr22:46537602-46537721 | Common:2; Rare:56 | ||||
| chr22:46762436-46762942 | Common:5; Rare:179 | ||||
| chr22:48489233-48489586 | Common:3; Rare:130 | ||||
| chr22:49827821-49827980 | Common:1; Rare:61 | ||||
| chr22:49917930-49918166 | Common:5; Rare:63 | ||||
| chr22:49918301-49918733 | Common:4; Rare:156; Clinvar (benign):3 | ||||
| chr22:49960295-49960509 | Common:1; Rare:75 | ||||
| chr22:50170598-50170832 | Rare:71 | ||||
| chr22:50185690-50186006 | Common:5; Rare:123 | ||||
| chr22:50200781-50201028 | Common:4; Rare:88 | ||||
| chr22:50244991-50245164 | Rare:68 | ||||
| chr22:50261641-50261996 | Common:4; Rare:108 | ||||
| chr22:50307563-50307836 | Common:8; Rare:56 |