| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50345926-50346136 | Common:4; Rare:69 | ||||
| chr17:50373160-50373254 | Common:3; Rare:42 | ||||
| chr17:50719456-50719652 | Rare:77 | ||||
| chr17:50866355-50866629 | Common:3; Rare:80 | ||||
| chr17:51260385-51260581 | Common:3; Rare:96 | ||||
| chr17:54968608-54968792 | Common:3; Rare:89 | ||||
| chr17:56914016-56914127 | Rare:30 | ||||
| chr17:57084980-57085105 | Rare:43 | ||||
| chr17:57850006-57850270 | Common:1; Rare:86 | ||||
| chr17:58352134-58352372 | Common:4; Rare:110 | ||||
| chr17:59106669-59106977 | Common:3; Rare:102; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:59155112-59155552 | Common:2; Rare:106 | ||||
| chr17:59155583-59155700 | Rare:32 | ||||
| chr17:59331481-59331763 | Common:2; Rare:92 | ||||
| chr17:59619569-59620010 | Common:3; Rare:157 |