| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44899388-44899736 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:45061103-45061339 | Common:1; Rare:67 | ||||
| chr17:47189235-47189579 | Rare:85 | ||||
| chr17:47831513-47831684 | Rare:49 | ||||
| chr17:47941352-47941726 | Rare:103; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48037666-48038023 | Common:7; Rare:69 | ||||
| chr17:48107681-48107784 | Common:1; Rare:25 | ||||
| chr17:48590239-48590428 | Common:1; Rare:42 | ||||
| chr17:48610531-48610684 | Rare:48 | ||||
| chr17:48944765-48944920 | Common:2; Rare:54 | ||||
| chr17:49788381-49788736 | Common:2; Rare:111 | ||||
| chr17:50188740-50189011 | Rare:72; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50189223-50189702 | Rare:105; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:50192473-50192694 | Common:1; Rare:49; Clinvar:3; Clinvar (benign):6 | ||||
| chr17:50192797-50193040 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 |