| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:13017957-13018255 | Common:5; Rare:84; Clinvar (benign):2 | ||||
| chr17:14069347-14069624 | Common:2; Rare:103; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:15260734-15260928 | Rare:75; Clinvar (benign):3 | ||||
| chr17:15262442-15262657 | Rare:48 | ||||
| chr17:15563446-15563755 | Common:1; Rare:100 | ||||
| chr17:15699506-15699774 | Common:3; Rare:72 | ||||
| chr17:15999583-16000032 | Common:3; Rare:190; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16215493-16215628 | Rare:64 | ||||
| chr17:16217092-16217259 | Rare:60; Clinvar:2 | ||||
| chr17:16380590-16381183 | Common:7; Rare:187 | ||||
| chr17:17281175-17281365 | Rare:73 | ||||
| chr17:17496388-17496575 | Common:2; Rare:51 | ||||
| chr17:17507057-17507263 | Common:4; Rare:62 | ||||
| chr17:17591573-17591926 | Common:2; Rare:103 | ||||
| chr17:18039039-18039390 | Common:3; Rare:86; Clinvar:1; Clinvar (benign):1 |