| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44899375-44899746 | Common:2; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:44947656-44947930 | Common:1; Rare:77 | ||||
| chr17:45061012-45061339 | Common:2; Rare:88 | ||||
| chr17:45132340-45132626 | Common:2; Rare:82 | ||||
| chr17:45148150-45148478 | Common:1; Rare:94 | ||||
| chr17:45161664-45161915 | Common:1; Rare:60 | ||||
| chr17:45490719-45490867 | Rare:51 | ||||
| chr17:46923071-46923181 | Common:1; Rare:49; Clinvar (benign):6 | ||||
| chr17:47649702-47649965 | Rare:107 | ||||
| chr17:47831507-47831656 | Rare:40 | ||||
| chr17:47941350-47941732 | Rare:103; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47970825-47971152 | Common:1; Rare:75 | ||||
| chr17:48048023-48048409 | Common:1; Rare:106 | ||||
| chr17:48048627-48048833 | Common:3; Rare:33 | ||||
| chr17:48544719-48544988 | Common:6; Rare:86 |