| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:49853469-49853929 | Common:10; Rare:741 | ||||
| chr22:49917443-49917843 | Common:5; Rare:84 | ||||
| chr22:49917980-49918231 | Common:6; Rare:107 | ||||
| chr22:49918273-49919242 | Common:43; Rare:1063; Clinvar (benign):11 | ||||
| chr22:49959998-49960917 | Common:25; Rare:1033 | ||||
| chr22:50085040-50085640 | Common:7; Rare:257; Clinvar:7; Clinvar (benign):3 | ||||
| chr22:50085650-50086072 | Common:10; Rare:277; Clinvar:20; Clinvar (benign):8 | ||||
| chr22:50170029-50170429 | Common:10; Rare:214 | ||||
| chr22:50170477-50170877 | Rare:163 | ||||
| chr22:50185624-50186024 | Common:20; Rare:454 | ||||
| chr22:50190255-50190655 | Common:11; Rare:239 | ||||
| chr22:50200550-50201095 | Common:24; Rare:519 | ||||
| chr22:50244172-50244788 | Common:10; Rare:524; Clinvar:4; Clinvar (benign):3 | ||||
| chr22:50244848-50246005 | Common:25; Rare:1072 | ||||
| chr22:50250380-50250870 | Common:6; Rare:258 |