| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43545862-43546139 | Common:2; Rare:42 | ||||
| chr17:43778896-43779049 | Rare:37 | ||||
| chr17:44066252-44066359 | Rare:37 | ||||
| chr17:44070583-44070958 | Common:3; Rare:127; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123608-44123849 | Common:3; Rare:68 | ||||
| chr17:44186687-44187050 | Common:1; Rare:119 | ||||
| chr17:44187162-44187515 | Common:1; Rare:81 | ||||
| chr17:44219466-44219985 | Common:1; Rare:187 | ||||
| chr17:44222073-44222333 | Rare:57 | ||||
| chr17:44324765-44324996 | Common:2; Rare:84 | ||||
| chr17:44345089-44345342 | Rare:51; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:44503374-44503686 | Rare:129 | ||||
| chr17:44899369-44899739 | Common:2; Rare:114; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:44968296-44968587 | Rare:80 | ||||
| chr17:45051368-45051680 | Common:1; Rare:98 |