| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42609326-42609745 | Common:8; Rare:179; Clinvar (benign):2 | ||||
| chr17:42659158-42659449 | Rare:88 | ||||
| chr17:42682462-42682588 | Rare:30 | ||||
| chr17:42745023-42745183 | Common:3; Rare:57 | ||||
| chr17:42760453-42760892 | Common:5; Rare:122 | ||||
| chr17:42760962-42761264 | Rare:77 | ||||
| chr17:42773338-42773484 | Rare:42 | ||||
| chr17:42798661-42798863 | Rare:63 | ||||
| chr17:42833085-42833161 | Rare:17 | ||||
| chr17:42833328-42833520 | Rare:69 | ||||
| chr17:42964428-42964547 | Rare:56 | ||||
| chr17:42980467-42980562 | Common:1; Rare:35 | ||||
| chr17:42998337-42998537 | Common:4; Rare:59 | ||||
| chr17:43022365-43022494 | Rare:34 | ||||
| chr17:43125317-43125694 | Rare:96; Clinvar:3; Clinvar (benign):3 |