| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45148167-45148625 | Common:1; Rare:160 | ||||
| chr17:46922869-46923212 | Common:4; Rare:104; Clinvar:3; Clinvar (benign):9 | ||||
| chr17:47323745-47323989 | Common:3; Rare:84 | ||||
| chr17:47649405-47649992 | Common:2; Rare:201 | ||||
| chr17:47650115-47650393 | Rare:105 | ||||
| chr17:47831477-47831656 | Rare:56 | ||||
| chr17:47941354-47941732 | Rare:102; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47970702-47971164 | Common:4; Rare:112 | ||||
| chr17:48048039-48048409 | Common:1; Rare:102 | ||||
| chr17:48048602-48048829 | Common:4; Rare:33 | ||||
| chr17:48107437-48107541 | Common:2; Rare:19 | ||||
| chr17:48107681-48107819 | Common:1; Rare:36 | ||||
| chr17:48543796-48544090 | Common:1; Rare:76 | ||||
| chr17:48544377-48544640 | Common:1; Rare:85 | ||||
| chr17:48544693-48544792 | Common:2; Rare:28 |