| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20508140-20508877 | Common:4; Rare:285 | ||||
| chr22:20858663-20859169 | Common:25; Rare:658; Clinvar:11; Clinvar (benign):16; Clinvar (pathogenic):2 | ||||
| chr22:20916668-20917170 | Common:13; Rare:165 | ||||
| chr22:20917215-20917574 | Rare:329 | ||||
| chr22:20917840-20918460 | Common:4; Rare:193 | ||||
| chr22:20981859-20982094 | Common:2; Rare:101; Clinvar (benign):1 | ||||
| chr22:20982124-20982369 | Common:6; Rare:168; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr22:21001545-21002359 | Common:22; Rare:485 | ||||
| chr22:21002284-21002684 | Common:4; Rare:152 | ||||
| chr22:21567252-21567857 | Common:8; Rare:232 | ||||
| chr22:21568120-21568610 | Common:7; Rare:180 | ||||
| chr22:21629923-21630229 | Common:5; Rare:271 | ||||
| chr22:21641948-21642405 | Common:6; Rare:355 | ||||
| chr22:21651901-21652244 | Common:4; Rare:182 | ||||
| chr22:21665923-21666125 | Common:1; Rare:154 |