| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45490678-45490949 | Common:7; Rare:85 | ||||
| chr17:45620171-45620485 | Common:1; Rare:70 | ||||
| chr17:45894189-45894532 | Common:3; Rare:111; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:46192498-46192661 | Common:3; Rare:32; Clinvar (benign):3 | ||||
| chr17:46193932-46194161 | Common:5; Rare:40 | ||||
| chr17:46194174-46194308 | Rare:15 | ||||
| chr17:46225226-46225576 | Common:4; Rare:81 | ||||
| chr17:46922781-46923284 | Common:5; Rare:163; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr17:46923531-46923630 | Rare:21 | ||||
| chr17:47188305-47188618 | Rare:50 | ||||
| chr17:47188880-47189670 | Common:4; Rare:199 | ||||
| chr17:47253871-47254034 | Common:3; Rare:54; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:47323635-47324051 | Common:5; Rare:142 | ||||
| chr17:47530960-47531217 | Rare:64 | ||||
| chr17:47649237-47649707 | Common:2; Rare:138 |