| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43546281-43546647 | Common:2; Rare:86 | ||||
| chr17:43661896-43662150 | Common:1; Rare:42 | ||||
| chr17:43900586-43900743 | Rare:48 | ||||
| chr17:44070624-44070954 | Common:3; Rare:120; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44111231-44111432 | Rare:56 | ||||
| chr17:44186658-44187002 | Common:1; Rare:127 | ||||
| chr17:44345072-44345321 | Rare:52; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:44503352-44503750 | Rare:148 | ||||
| chr17:44899374-44899736 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:44947679-44947903 | Common:1; Rare:61 | ||||
| chr17:45060964-45061339 | Common:2; Rare:98 | ||||
| chr17:45148147-45148478 | Common:1; Rare:94 | ||||
| chr17:45894278-45894572 | Common:3; Rare:86; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:46225353-46225521 | Common:3; Rare:46 | ||||
| chr17:46922858-46923190 | Common:4; Rare:93; Clinvar:1; Clinvar (benign):7 |