| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:45671745-45672076 | Common:8; Rare:286 | ||||
| chr22:45672140-45672580 | Common:5; Rare:194 | ||||
| chr22:45672634-45672924 | Common:6; Rare:65 | ||||
| chr22:45977071-45977289 | Common:3; Rare:116 | ||||
| chr22:46053715-46053929 | Rare:163 | ||||
| chr22:46054128-46054490 | Common:12; Rare:206 | ||||
| chr22:46150281-46150561 | Common:2; Rare:174 | ||||
| chr22:46250080-46250490 | Common:11; Rare:250 | ||||
| chr22:46250987-46251155 | Common:1; Rare:45 | ||||
| chr22:46267758-46268083 | Common:4; Rare:219 | ||||
| chr22:46296465-46297564 | Common:18; Rare:483 | ||||
| chr22:46335552-46336042 | Common:23; Rare:464; Clinvar:33; Clinvar (benign):31; Clinvar (pathogenic):5 | ||||
| chr22:46350085-46350866 | Common:15; Rare:398; Clinvar:10; Clinvar (benign):10; Clinvar (pathogenic):4 | ||||
| chr22:46377540-46377901 | Common:13; Rare:153 | ||||
| chr22:46536329-46536983 | Common:5; Rare:248 |