| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:46922869-46923187 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47188830-47188935 | Rare:14 | ||||
| chr17:47189187-47189619 | Common:1; Rare:116 | ||||
| chr17:47323864-47323992 | Common:1; Rare:44 | ||||
| chr17:47649534-47649927 | Common:1; Rare:140 | ||||
| chr17:47941382-47941733 | Rare:97; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048061-48048405 | Rare:92 | ||||
| chr17:48048630-48048813 | Common:3; Rare:25 | ||||
| chr17:48101377-48101620 | Common:2; Rare:78 | ||||
| chr17:48613465-48613760 | Common:4; Rare:87 | ||||
| chr17:48614279-48614286 | Rare:1 | ||||
| chr17:48614360-48614447 | Rare:38 | ||||
| chr17:48908606-48908729 | Rare:24 | ||||
| chr17:48944765-48944901 | Common:1; Rare:48 | ||||
| chr17:49210141-49210436 | Common:2; Rare:47 |