| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46267804-46268070 | Common:1; Rare:83 | ||||
| chr22:46296739-46296924 | Common:1; Rare:62 | ||||
| chr22:46335621-46335922 | Common:8; Rare:139; Clinvar:9; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr22:46377588-46377839 | Common:5; Rare:62 | ||||
| chr22:46762496-46762703 | Common:3; Rare:77 | ||||
| chr22:49918373-49918702 | Common:2; Rare:125; Clinvar (benign):1 | ||||
| chr22:50185708-50185953 | Common:4; Rare:103 | ||||
| chr22:50190314-50190613 | Common:4; Rare:85 | ||||
| chr22:50206132-50206309 | Common:1; Rare:54 | ||||
| chr22:50525531-50525683 | Common:4; Rare:75; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50530953-50531168 | Rare:70 | ||||
| chr22:50532117-50532178 | Rare:13 | ||||
| chr22:50562887-50563080 | Common:3; Rare:51 | ||||
| chr22:50582365-50582429 | Rare:28 | ||||
| chr22:50582794-50583151 | Common:8; Rare:121; Clinvar:2; Clinvar (benign):3 |