| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42833365-42833505 | Rare:53 | ||||
| chr17:43125338-43125590 | Rare:54; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170292-43170479 | Common:2; Rare:37 | ||||
| chr17:43170962-43171274 | Common:1; Rare:107 | ||||
| chr17:43211748-43211912 | Common:2; Rare:36 | ||||
| chr17:43778922-43779055 | Rare:28 | ||||
| chr17:44070619-44070947 | Common:3; Rare:115; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44111225-44111319 | Rare:27 | ||||
| chr17:44123571-44123840 | Common:3; Rare:77 | ||||
| chr17:44186668-44187033 | Common:1; Rare:126 | ||||
| chr17:44187178-44187274 | Rare:26 | ||||
| chr17:44324750-44325023 | Common:2; Rare:98 | ||||
| chr17:44345067-44345321 | Rare:52; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:44503377-44503731 | Rare:136 | ||||
| chr17:44557094-44557349 | Common:1; Rare:46 |