| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:64503991-64504341 | Common:2; Rare:122 | ||||
| chr17:64534457-64534728 | Rare:101 | ||||
| chr17:64662266-64662449 | Common:1; Rare:91 | ||||
| chr17:65137262-65137448 | Common:1; Rare:66 | ||||
| chr17:66302453-66302616 | Common:1; Rare:76 | ||||
| chr17:67245169-67245282 | Rare:37 | ||||
| chr17:67366430-67366702 | Common:1; Rare:89 | ||||
| chr17:67377150-67377401 | Common:1; Rare:62 | ||||
| chr17:67377792-67378066 | Common:1; Rare:69 | ||||
| chr17:67717744-67718097 | Rare:113 | ||||
| chr17:68042793-68042999 | Common:3; Rare:73 | ||||
| chr17:68247987-68248227 | Common:4; Rare:89 | ||||
| chr17:68511871-68512111 | Common:1; Rare:56 | ||||
| chr17:68512302-68512513 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:68512605-68512742 | Rare:47 |