| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49763255-49764131 | Common:4; Rare:334 | ||||
| chr17:49764157-49764796 | Common:2; Rare:245 | ||||
| chr17:49788375-49788818 | Common:8; Rare:635 | ||||
| chr17:49788898-49789380 | Common:7; Rare:330 | ||||
| chr17:49968310-49968784 | Common:4; Rare:189 | ||||
| chr17:49968970-49969360 | Common:8; Rare:289 | ||||
| chr17:49971650-49972090 | Common:1; Rare:164 | ||||
| chr17:50149755-50150257 | Common:22; Rare:209; Clinvar:9 | ||||
| chr17:50151004-50151295 | Common:1; Rare:164 | ||||
| chr17:50199657-50200057 | Common:7; Rare:154; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:50274184-50274602 | Common:7; Rare:407 | ||||
| chr17:50345800-50346190 | Common:21; Rare:413 | ||||
| chr17:50372760-50373490 | Common:29; Rare:818 | ||||
| chr17:50384851-50385450 | Common:11; Rare:263 | ||||
| chr17:50396705-50397105 | Common:2; Rare:83 |