| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45490695-45490954 | Common:7; Rare:83 | ||||
| chr17:45894080-45894572 | Common:6; Rare:146; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:46192846-46193058 | Common:1; Rare:53 | ||||
| chr17:46193062-46193132 | Common:2; Rare:15 | ||||
| chr17:46193284-46193670 | Common:8; Rare:107 | ||||
| chr17:46193943-46194140 | Common:4; Rare:35 | ||||
| chr17:46225359-46225545 | Common:4; Rare:52 | ||||
| chr17:46851357-46851636 | Common:2; Rare:73 | ||||
| chr17:46922787-46923246 | Common:5; Rare:146; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr17:46923608-46923833 | Common:3; Rare:55 | ||||
| chr17:47188979-47189051 | Rare:18 | ||||
| chr17:47189075-47189143 | Rare:21 | ||||
| chr17:47189171-47189662 | Common:1; Rare:130 | ||||
| chr17:47253751-47253828 | Common:1; Rare:16 | ||||
| chr17:47253862-47253994 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):3 |