| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:72120777-72121068 | Rare:77 | ||||
| chr17:72121173-72121316 | Common:2; Rare:38; Clinvar:3; Clinvar (benign):4 | ||||
| chr17:72121497-72121829 | Rare:70; Clinvar (benign):1 | ||||
| chr17:73092620-73092776 | Common:2; Rare:39 | ||||
| chr17:73192516-73192725 | Common:5; Rare:53 | ||||
| chr17:73192742-73193155 | Common:16; Rare:159; Clinvar:6; Clinvar (benign):1 | ||||
| chr17:73193252-73193395 | Rare:53; Clinvar:4 | ||||
| chr17:73193527-73193686 | Rare:34 | ||||
| chr17:73232227-73232481 | Common:1; Rare:105 | ||||
| chr17:73233099-73233274 | Common:2; Rare:41 | ||||
| chr17:73310655-73310904 | Common:2; Rare:60 | ||||
| chr17:73310963-73311304 | Common:1; Rare:81 | ||||
| chr17:73311551-73311666 | Common:2; Rare:23 | ||||
| chr17:73311903-73312166 | Rare:69 | ||||
| chr17:73312169-73312305 | Rare:30 |