| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:73164879-73165012 | Common:2; Rare:42 | ||||
| chr17:73191696-73192520 | Common:8; Rare:180 | ||||
| chr17:73192584-73192707 | Common:3; Rare:31 | ||||
| chr17:73192749-73193110 | Common:15; Rare:141; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:73232242-73232445 | Rare:90 | ||||
| chr17:73233287-73233687 | Common:3; Rare:110 | ||||
| chr17:73262130-73262700 | Common:3; Rare:116 | ||||
| chr17:73310135-73310363 | Rare:32 | ||||
| chr17:73310956-73311629 | Common:2; Rare:247 | ||||
| chr17:73311985-73312166 | Rare:46 | ||||
| chr17:73643915-73644063 | Common:1; Rare:41 | ||||
| chr17:73644432-73644572 | Common:1; Rare:34 | ||||
| chr17:74203376-74203774 | Common:3; Rare:117 | ||||
| chr17:74213397-74213575 | Common:3; Rare:44 | ||||
| chr17:74274090-74274360 | Common:3; Rare:52; Clinvar:2; Clinvar (benign):2 |