| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44198737-44198845 | Rare:36 | ||||
| chr17:44210838-44211183 | Common:1; Rare:104 | ||||
| chr17:44221211-44221364 | Rare:46 | ||||
| chr17:44324657-44324997 | Common:4; Rare:112 | ||||
| chr17:44350437-44350801 | Rare:127; Clinvar:9; Clinvar (benign):5 | ||||
| chr17:44351032-44351647 | Common:1; Rare:173; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr17:44351649-44352042 | Rare:121; Clinvar:7 | ||||
| chr17:44503366-44503719 | Rare:136 | ||||
| chr17:44899374-44899759 | Common:3; Rare:121; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:44947641-44947892 | Common:1; Rare:62 | ||||
| chr17:45051410-45051696 | Common:1; Rare:92 | ||||
| chr17:45060937-45061339 | Common:3; Rare:102 | ||||
| chr17:45148148-45148641 | Common:1; Rare:165 | ||||
| chr17:45161568-45161915 | Common:1; Rare:85 | ||||
| chr17:45431915-45432069 | Common:2; Rare:21 |