| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44220813-44221087 | Rare:92 | ||||
| chr17:44268096-44268417 | Rare:64; Clinvar:3 | ||||
| chr17:44324735-44324993 | Common:3; Rare:96 | ||||
| chr17:44503366-44503713 | Rare:134 | ||||
| chr17:44899375-44899741 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:45060964-45061339 | Common:2; Rare:98 | ||||
| chr17:45148152-45148489 | Common:1; Rare:101 | ||||
| chr17:45490719-45490867 | Rare:51 | ||||
| chr17:46922869-46923187 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47188839-47188916 | Rare:11 | ||||
| chr17:47189207-47189523 | Common:1; Rare:85 | ||||
| chr17:47323838-47324013 | Common:3; Rare:67 | ||||
| chr17:47649630-47649969 | Common:1; Rare:131 | ||||
| chr17:47650136-47650393 | Rare:100 | ||||
| chr17:47831513-47831646 | Rare:34 |