| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44070612-44070922 | Common:3; Rare:105; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44186695-44187002 | Rare:102 | ||||
| chr17:44220845-44221025 | Rare:54 | ||||
| chr17:44324765-44324946 | Common:1; Rare:67 | ||||
| chr17:44899374-44899729 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:45060993-45061332 | Common:2; Rare:89 | ||||
| chr17:45490719-45490887 | Rare:56 | ||||
| chr17:46225353-46225458 | Common:1; Rare:31 | ||||
| chr17:46923084-46923179 | Common:1; Rare:38; Clinvar (benign):6 | ||||
| chr17:47831516-47831656 | Rare:36 | ||||
| chr17:47941382-47941712 | Rare:92; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048092-48048409 | Rare:76 | ||||
| chr17:48048643-48048812 | Common:3; Rare:22 | ||||
| chr17:48590200-48590428 | Common:1; Rare:51 | ||||
| chr17:48610556-48610673 | Rare:37 |