| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4967748-4968016 | Common:1; Rare:98 | ||||
| chr17:4987621-4987814 | Common:2; Rare:66 | ||||
| chr17:4997900-4998154 | Common:2; Rare:101; Clinvar (benign):1 | ||||
| chr17:5078372-5078524 | Common:4; Rare:49 | ||||
| chr17:5191824-5192112 | Common:2; Rare:89 | ||||
| chr17:5234816-5234976 | Rare:35 | ||||
| chr17:5419618-5419882 | Common:3; Rare:89 | ||||
| chr17:5420129-5420227 | Rare:39 | ||||
| chr17:5486163-5486577 | Common:5; Rare:139 | ||||
| chr17:5486778-5486930 | Common:4; Rare:49 | ||||
| chr17:6556383-6556714 | Common:2; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:6640651-6641090 | Common:7; Rare:138 | ||||
| chr17:6651558-6651747 | Common:1; Rare:65 | ||||
| chr17:7012315-7012758 | Rare:146 | ||||
| chr17:7219841-7219981 | Common:3; Rare:67; Clinvar:6; Clinvar (benign):2 |