| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1628812-1629134 | Rare:105 | ||||
| chr17:1629157-1629383 | Rare:46 | ||||
| chr17:1643899-1644093 | Common:1; Rare:34 | ||||
| chr17:1644101-1644148 | Rare:9 | ||||
| chr17:1644507-1644853 | Common:4; Rare:73 | ||||
| chr17:1645660-1645956 | Common:4; Rare:76 | ||||
| chr17:1648864-1649275 | Common:4; Rare:149 | ||||
| chr17:1649489-1649695 | Common:2; Rare:81 | ||||
| chr17:1684395-1684519 | Common:1; Rare:51; Clinvar:1 | ||||
| chr17:1684754-1685096 | Common:3; Rare:120; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:1716149-1716571 | Common:4; Rare:139 | ||||
| chr17:1716574-1716781 | Common:1; Rare:56 | ||||
| chr17:1716783-1716882 | Rare:26 | ||||
| chr17:1716994-1717374 | Common:1; Rare:76 | ||||
| chr17:1724524-1724820 | Common:2; Rare:99 |