| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49209202-49209456 | Common:2; Rare:47 | ||||
| chr17:49210210-49210484 | Common:2; Rare:43 | ||||
| chr17:49210503-49210713 | Rare:36 | ||||
| chr17:49362251-49362424 | Common:3; Rare:52 | ||||
| chr17:49414810-49415172 | Common:3; Rare:93 | ||||
| chr17:49788567-49788831 | Common:1; Rare:90 | ||||
| chr17:50055682-50056604 | Common:7; Rare:218 | ||||
| chr17:50063886-50064143 | Common:1; Rare:43 | ||||
| chr17:50076350-50076678 | Common:3; Rare:116; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:50094463-50094594 | Rare:24 | ||||
| chr17:50186639-50187113 | Common:2; Rare:140; Clinvar:7; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr17:50188743-50189415 | Rare:167; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr17:50190571-50190926 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:50195230-50195474 | Rare:71; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:50197016-50197236 | Rare:56; Clinvar:2; Clinvar (benign):2 |