| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47896494-47896565 | Rare:18 | ||||
| chr17:47941348-47941758 | Rare:108; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47957733-47958118 | Common:3; Rare:66 | ||||
| chr17:48048057-48048405 | Rare:93 | ||||
| chr17:48048643-48048833 | Common:3; Rare:30 | ||||
| chr17:48107691-48107802 | Common:1; Rare:27 | ||||
| chr17:48544693-48545018 | Common:8; Rare:102 | ||||
| chr17:48908295-48908407 | Common:1; Rare:27 | ||||
| chr17:48944765-48944888 | Common:1; Rare:44 | ||||
| chr17:49210228-49210432 | Common:2; Rare:29 | ||||
| chr17:49210581-49210718 | Rare:20 | ||||
| chr17:49677961-49678261 | Rare:71 | ||||
| chr17:49708144-49708321 | Rare:55 | ||||
| chr17:49788546-49788745 | Common:1; Rare:63 | ||||
| chr17:49995194-49995458 | Common:4; Rare:46; Clinvar:1 |