| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5420119-5420225 | Rare:43 | ||||
| chr17:5433297-5433564 | Common:1; Rare:71; Clinvar (pathogenic):1 | ||||
| chr17:5486160-5486393 | Common:4; Rare:103 | ||||
| chr17:5486517-5486929 | Common:7; Rare:118 | ||||
| chr17:6640641-6641077 | Common:7; Rare:133 | ||||
| chr17:6651542-6651767 | Common:1; Rare:77 | ||||
| chr17:7012315-7012734 | Rare:136 | ||||
| chr17:7219826-7220039 | Common:4; Rare:90; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7221254-7221637 | Common:9; Rare:116; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr17:7221737-7221993 | Common:3; Rare:61; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr17:7222321-7222815 | Common:4; Rare:157; Clinvar:11; Clinvar (pathogenic):8 | ||||
| chr17:7223068-7223369 | Rare:113; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr17:7223942-7224234 | Rare:106; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):10 | ||||
| chr17:7224302-7224910 | Common:4; Rare:221; Clinvar:17; Clinvar (benign):25; Clinvar (pathogenic):4 | ||||
| chr17:7234457-7234634 | Common:2; Rare:93 |