| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42649311-42649482 | Common:1; Rare:67 | ||||
| chr22:42857184-42857471 | Common:3; Rare:119 | ||||
| chr22:43015086-43015384 | Common:2; Rare:122 | ||||
| chr22:43812279-43812431 | Common:1; Rare:50 | ||||
| chr22:43955291-43955562 | Common:3; Rare:81 | ||||
| chr22:44024185-44024426 | Common:1; Rare:78 | ||||
| chr22:44312805-44312936 | Rare:33 | ||||
| chr22:45163747-45164216 | Common:6; Rare:186 | ||||
| chr22:45671972-45672058 | Rare:38 | ||||
| chr22:46053786-46053901 | Rare:40 | ||||
| chr22:46250254-46250385 | Common:2; Rare:36 | ||||
| chr22:46267865-46268037 | Common:1; Rare:54 | ||||
| chr22:46335632-46335776 | Common:4; Rare:61; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr22:46762450-46762670 | Common:3; Rare:82 | ||||
| chr22:49918408-49918710 | Common:1; Rare:113 |