| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47531321-47531454 | Common:1; Rare:44 | ||||
| chr17:47649534-47649849 | Common:1; Rare:94 | ||||
| chr17:47649888-47649980 | Rare:47 | ||||
| chr17:47679846-47680103 | Common:1; Rare:55 | ||||
| chr17:47831503-47831614 | Rare:33 | ||||
| chr17:47941358-47941732 | Rare:102; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47957090-47957453 | Common:1; Rare:68 | ||||
| chr17:47957650-47957995 | Common:2; Rare:53 | ||||
| chr17:47970732-47971170 | Common:4; Rare:108 | ||||
| chr17:48048039-48048405 | Common:1; Rare:100 | ||||
| chr17:48048668-48048916 | Common:4; Rare:46 | ||||
| chr17:48107689-48107802 | Common:1; Rare:27 | ||||
| chr17:48610525-48610706 | Common:1; Rare:60 | ||||
| chr17:48625845-48625922 | Rare:25 | ||||
| chr17:48830996-48831069 | Common:1; Rare:22 |