| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:64130692-64130786 | Rare:19 | ||||
| chr17:64497017-64497150 | Common:1; Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:64506159-64506815 | Common:8; Rare:266 | ||||
| chr17:64662297-64662459 | Common:1; Rare:83 | ||||
| chr17:65056577-65056911 | Common:4; Rare:130 | ||||
| chr17:67245165-67245351 | Rare:58 | ||||
| chr17:67366442-67366710 | Rare:88 | ||||
| chr17:67717740-67717972 | Rare:80 | ||||
| chr17:68247886-68248142 | Common:6; Rare:105 | ||||
| chr17:68512284-68512548 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:68512621-68512936 | Rare:115 | ||||
| chr17:68955334-68955459 | Rare:25 | ||||
| chr17:72120793-72121029 | Rare:62 | ||||
| chr17:73232137-73232726 | Common:4; Rare:226 | ||||
| chr17:73311973-73312207 | Rare:58 |