| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68126768-68127054 | Common:2; Rare:60 | ||||
| chr17:68128861-68129143 | Common:1; Rare:48 | ||||
| chr17:68129372-68129401 | Common:1; Rare:3 | ||||
| chr17:68137982-68138149 | Common:3; Rare:30 | ||||
| chr17:68205281-68205500 | Common:7; Rare:60 | ||||
| chr17:68205997-68206086 | Common:3; Rare:20 | ||||
| chr17:68301763-68301919 | Common:1; Rare:28 | ||||
| chr17:68302244-68302541 | Common:2; Rare:54 | ||||
| chr17:68426091-68426253 | Common:3; Rare:77 | ||||
| chr17:68452959-68453241 | Common:2; Rare:49 | ||||
| chr17:68519482-68519636 | Common:1; Rare:29 | ||||
| chr17:68520330-68520455 | Rare:17 | ||||
| chr17:68522739-68522765 | Rare:8; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:68523723-68524136 | Common:3; Rare:109; Clinvar:2; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:68524902-68525046 | Rare:31; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 |