| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2400746-2400788 | Rare:9 | ||||
| chr17:2511766-2511930 | Common:2; Rare:42 | ||||
| chr17:2593464-2593690 | Common:3; Rare:86; Clinvar (benign):2 | ||||
| chr17:2593857-2594001 | Common:1; Rare:38; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:2711742-2712052 | Common:2; Rare:87 | ||||
| chr17:2796202-2796478 | Common:1; Rare:64 | ||||
| chr17:3636215-3636507 | Common:4; Rare:88; Clinvar (benign):1 | ||||
| chr17:3636691-3636814 | Common:1; Rare:35; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:3668452-3668829 | Common:3; Rare:156 | ||||
| chr17:3723723-3723922 | Common:1; Rare:104 | ||||
| chr17:3845904-3846042 | Rare:35 | ||||
| chr17:3892949-3893271 | Common:3; Rare:111 | ||||
| chr17:3916414-3916628 | Common:1; Rare:43 | ||||
| chr17:3964223-3964551 | Common:3; Rare:105 | ||||
| chr17:4032977-4033065 | Rare:21 |