| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:61863283-61863362 | Rare:17; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:61863376-61863797 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:61926991-61927284 | Rare:56 | ||||
| chr17:61927389-61927614 | Common:1; Rare:52 | ||||
| chr17:61927865-61928156 | Common:3; Rare:107 | ||||
| chr17:62064920-62064961 | Rare:9 | ||||
| chr17:62065052-62065182 | Rare:46 | ||||
| chr17:62065651-62066011 | Common:3; Rare:110 | ||||
| chr17:62423713-62424069 | Common:2; Rare:129 | ||||
| chr17:62478132-62478238 | Common:1; Rare:29 | ||||
| chr17:62478450-62478888 | Common:4; Rare:124 | ||||
| chr17:62627478-62627708 | Common:1; Rare:69 | ||||
| chr17:63445706-63445757 | Common:1; Rare:11 | ||||
| chr17:63445761-63445853 | Rare:16 | ||||
| chr17:63446075-63446462 | Common:1; Rare:119 |