| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49210591-49210718 | Rare:20 | ||||
| chr17:49362136-49362375 | Common:3; Rare:95 | ||||
| chr17:49708150-49708379 | Common:1; Rare:72 | ||||
| chr17:49788552-49788777 | Common:1; Rare:76 | ||||
| chr17:50055762-50056155 | Common:4; Rare:84 | ||||
| chr17:50095553-50095630 | Rare:18 | ||||
| chr17:50194615-50194803 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr17:50274424-50274494 | Rare:19 | ||||
| chr17:50373151-50373246 | Common:3; Rare:42 | ||||
| chr17:50397437-50397693 | Common:2; Rare:67 | ||||
| chr17:50426070-50426315 | Common:1; Rare:64 | ||||
| chr17:50463790-50464074 | Rare:70 | ||||
| chr17:50465027-50465072 | Rare:8 | ||||
| chr17:50634778-50635100 | Common:2; Rare:77 | ||||
| chr17:50657694-50658032 | Rare:61 |