| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43211640-43211898 | Common:2; Rare:59 | ||||
| chr17:43483661-43484034 | Rare:103 | ||||
| chr17:43778917-43779081 | Rare:38 | ||||
| chr17:44070636-44070947 | Common:3; Rare:110; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123636-44123883 | Common:3; Rare:64 | ||||
| chr17:44186672-44187002 | Common:1; Rare:117 | ||||
| chr17:44187184-44187283 | Rare:26 | ||||
| chr17:44221273-44221427 | Rare:46 | ||||
| chr17:44324765-44324966 | Common:2; Rare:73 | ||||
| chr17:44503377-44503714 | Rare:132 | ||||
| chr17:44899367-44899799 | Common:3; Rare:132; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:45060992-45061339 | Common:2; Rare:91 | ||||
| chr17:45148165-45148623 | Common:1; Rare:160 | ||||
| chr17:45161530-45161804 | Common:1; Rare:61 | ||||
| chr17:45490713-45490867 | Rare:53 |