| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:64391200-64391628 | Common:8; Rare:173 | ||||
| chr17:64448760-64449240 | Common:11; Rare:190 | ||||
| chr17:64496730-64496832 | Rare:39; Clinvar (benign):1 | ||||
| chr17:64496940-64497277 | Common:12; Rare:643; Clinvar:18; Clinvar (benign):18 | ||||
| chr17:64504754-64506101 | Common:69; Rare:2248 | ||||
| chr17:64506083-64507756 | Common:53; Rare:1956 | ||||
| chr17:64661486-64661886 | Common:5; Rare:133 | ||||
| chr17:64662069-64662173 | Rare:38 | ||||
| chr17:64662193-64662682 | Common:5; Rare:473 | ||||
| chr17:64918770-64919185 | Common:5; Rare:234 | ||||
| chr17:64919322-64919801 | Common:60; Rare:476 | ||||
| chr17:65055662-65056486 | Common:11; Rare:477 | ||||
| chr17:65056492-65057129 | Common:28; Rare:1010 | ||||
| chr17:65137026-65137462 | Common:8; Rare:222 | ||||
| chr17:65560874-65561274 | Common:1; Rare:232 |