| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42744530-42744820 | Rare:102 | ||||
| chr17:42745002-42745183 | Common:6; Rare:128 | ||||
| chr17:42773358-42773497 | Rare:83 | ||||
| chr17:42798665-42798863 | Rare:92 | ||||
| chr17:42832930-42833512 | Common:2; Rare:245 | ||||
| chr17:42964333-42964603 | Common:1; Rare:166 | ||||
| chr17:42980394-42980582 | Common:2; Rare:109 | ||||
| chr17:42980650-42981163 | Common:2; Rare:182 | ||||
| chr17:42997970-42998556 | Common:9; Rare:207 | ||||
| chr17:43022329-43022494 | Rare:89 | ||||
| chr17:43125091-43125729 | Common:1; Rare:271; Clinvar:12; Clinvar (benign):16 | ||||
| chr17:43170182-43170522 | Common:4; Rare:146 | ||||
| chr17:43170960-43171305 | Common:2; Rare:212 | ||||
| chr17:43398876-43399019 | Common:2; Rare:83 | ||||
| chr17:43483611-43484028 | Rare:210 |