| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1078949-1079053 | Rare:36 | ||||
| chr17:1491615-1491889 | Common:1; Rare:81 | ||||
| chr17:1492631-1492783 | Rare:32 | ||||
| chr17:1516578-1516995 | Common:2; Rare:147 | ||||
| chr17:1645720-1645965 | Common:2; Rare:48 | ||||
| chr17:1648851-1649195 | Common:3; Rare:117 | ||||
| chr17:1684792-1685038 | Common:2; Rare:80; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1829779-1830072 | Common:8; Rare:124 | ||||
| chr17:2030012-2030166 | Common:1; Rare:56 | ||||
| chr17:2303722-2303987 | Common:2; Rare:101 | ||||
| chr17:2336430-2336550 | Rare:46 | ||||
| chr17:2511766-2511947 | Common:2; Rare:48 | ||||
| chr17:2593486-2593658 | Common:2; Rare:64 | ||||
| chr17:2593857-2593987 | Common:1; Rare:38; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:2711781-2712043 | Common:2; Rare:71 |