| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43170268-43170554 | Common:3; Rare:58 | ||||
| chr17:43171024-43171245 | Rare:68 | ||||
| chr17:44070619-44070947 | Common:3; Rare:115; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44186688-44187060 | Common:1; Rare:118 | ||||
| chr17:44324771-44324982 | Common:2; Rare:76 | ||||
| chr17:44350506-44350735 | Rare:78; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:44503374-44503639 | Rare:116 | ||||
| chr17:44899383-44899729 | Common:2; Rare:108; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:45060987-45061339 | Common:2; Rare:93 | ||||
| chr17:45148164-45148478 | Common:1; Rare:93 | ||||
| chr17:47189250-47189587 | Rare:85 | ||||
| chr17:47941368-47941702 | Rare:91; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048638-48048821 | Common:3; Rare:26 | ||||
| chr17:48944783-48944918 | Common:2; Rare:39 | ||||
| chr17:50189223-50189480 | Rare:57; Clinvar:3; Clinvar (benign):1 |