| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48610537-48610705 | Common:1; Rare:57 | ||||
| chr17:48892366-48892509 | Common:7; Rare:54 | ||||
| chr17:48944754-48944937 | Common:2; Rare:67 | ||||
| chr17:49414828-49415134 | Common:2; Rare:72 | ||||
| chr17:49708132-49708327 | Common:1; Rare:62 | ||||
| chr17:49788470-49788718 | Common:1; Rare:78 | ||||
| chr17:50056421-50056458 | Rare:11 | ||||
| chr17:50095163-50095402 | Common:1; Rare:70 | ||||
| chr17:50188527-50189172 | Rare:167; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
| chr17:50189174-50189684 | Rare:114; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:50191835-50191993 | Common:1; Rare:46; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr17:50192825-50193040 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:50195432-50195598 | Rare:35; Clinvar (benign):2 | ||||
| chr17:50196499-50196647 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:50373151-50373277 | Common:3; Rare:54 |