| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80261646-80262114 | Common:8; Rare:107 | ||||
| chr17:80307884-80307916 | Rare:8 | ||||
| chr17:80367550-80367682 | Rare:37 | ||||
| chr17:80367839-80368141 | Common:1; Rare:84; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr17:80383516-80383798 | Common:1; Rare:78 | ||||
| chr17:80413896-80414027 | Rare:38 | ||||
| chr17:80782630-80782818 | Common:1; Rare:39 | ||||
| chr17:80789680-80789906 | Common:1; Rare:36 | ||||
| chr17:80791953-80792224 | Rare:54 | ||||
| chr17:80927985-80928001 | Rare:1 | ||||
| chr17:81029165-81029285 | Rare:26 | ||||
| chr17:81251566-81251677 | Rare:40 | ||||
| chr17:81397140-81397272 | Rare:42 | ||||
| chr17:81456833-81457078 | Common:1; Rare:60 | ||||
| chr17:81510803-81510877 | Common:1; Rare:33; Clinvar:1; Clinvar (benign):4 |