| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8186219-8186357 | Common:1; Rare:46 | ||||
| chr17:8186833-8186945 | Common:1; Rare:81 | ||||
| chr17:8189471-8190404 | Common:2; Rare:622 | ||||
| chr17:8192190-8192450 | Common:8; Rare:111 | ||||
| chr17:8200150-8200400 | Common:2; Rare:169 | ||||
| chr17:8220730-8221100 | Common:9; Rare:248 | ||||
| chr17:8222384-8222770 | Common:4; Rare:120 | ||||
| chr17:8222880-8223270 | Common:4; Rare:321 | ||||
| chr17:8223420-8223600 | Common:4; Rare:57 | ||||
| chr17:8236970-8237530 | Common:2; Rare:174; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr17:8375790-8376050 | Common:1; Rare:51 | ||||
| chr17:8631302-8631475 | Rare:92 | ||||
| chr17:9050671-9051110 | Common:14; Rare:266 | ||||
| chr17:9051159-9051559 | Common:1; Rare:100 | ||||
| chr17:9054220-9054610 | Common:6; Rare:151 |