| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50278562-50279027 | Common:1; Rare:141 | ||||
| chr22:50280487-50280919 | Common:4; Rare:134 | ||||
| chr22:50280955-50281164 | Rare:79 | ||||
| chr22:50281795-50282409 | Common:6; Rare:200 | ||||
| chr22:50285988-50286295 | Common:1; Rare:108 | ||||
| chr22:50301639-50301890 | Common:1; Rare:53 | ||||
| chr22:50301906-50302178 | Common:1; Rare:61 | ||||
| chr22:50443321-50443533 | Common:3; Rare:72 | ||||
| chr22:50454812-50455067 | Rare:107; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:50455107-50455257 | Rare:58 | ||||
| chr22:50525532-50525718 | Common:4; Rare:91; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50526728-50526798 | Rare:29 | ||||
| chr22:50532140-50532251 | Rare:26 | ||||
| chr22:50562887-50563065 | Common:3; Rare:47 | ||||
| chr22:50579243-50579277 | Rare:11; Clinvar:1 |