| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1829766-1830039 | Common:7; Rare:116 | ||||
| chr17:2041268-2041536 | Common:2; Rare:92 | ||||
| chr17:2303305-2303401 | Rare:36 | ||||
| chr17:2303450-2303639 | Rare:70 | ||||
| chr17:2303722-2303987 | Common:2; Rare:101 | ||||
| chr17:2336423-2336551 | Rare:50 | ||||
| chr17:2511778-2512021 | Common:2; Rare:72 | ||||
| chr17:2593470-2593709 | Common:3; Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:2593875-2593998 | Common:1; Rare:32; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:2711762-2712073 | Common:2; Rare:82 | ||||
| chr17:2796324-2796498 | Rare:51 | ||||
| chr17:3557796-3557950 | Common:4; Rare:30; Clinvar:4; Clinvar (benign):4 | ||||
| chr17:3636193-3636779 | Common:8; Rare:170; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:3668489-3668826 | Common:3; Rare:139 | ||||
| chr17:3696106-3696194 | Rare:23 |