| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2303751-2303980 | Common:2; Rare:88 | ||||
| chr17:2336423-2336512 | Rare:33 | ||||
| chr17:2337429-2337718 | Common:1; Rare:97 | ||||
| chr17:2511812-2511997 | Common:2; Rare:54 | ||||
| chr17:2593507-2593658 | Common:2; Rare:48 | ||||
| chr17:2711717-2712031 | Common:2; Rare:89 | ||||
| chr17:3636241-3636541 | Common:4; Rare:84; Clinvar (benign):1 | ||||
| chr17:3636712-3636814 | Common:1; Rare:28; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:3668545-3668824 | Common:2; Rare:110 | ||||
| chr17:3723802-3723917 | Rare:63 | ||||
| chr17:3892971-3893282 | Common:2; Rare:104 | ||||
| chr17:4142991-4143225 | Rare:82 | ||||
| chr17:4143605-4143733 | Common:4; Rare:74 | ||||
| chr17:4533106-4533360 | Rare:113 | ||||
| chr17:4704116-4704203 | Rare:55 |