| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63773470-63773858 | Common:2; Rare:126 | ||||
| chr17:64020591-64020823 | Common:2; Rare:41 | ||||
| chr17:64390642-64390957 | Common:1; Rare:56 | ||||
| chr17:64497044-64497082 | Common:1; Rare:12; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:64506617-64506789 | Common:2; Rare:67 | ||||
| chr17:67245152-67245339 | Rare:60 | ||||
| chr17:67717743-67717950 | Rare:66 | ||||
| chr17:68247813-68248114 | Common:5; Rare:137 | ||||
| chr17:68512302-68512495 | Common:1; Rare:66; Clinvar (benign):1 | ||||
| chr17:68543068-68543350 | Common:1; Rare:57 | ||||
| chr17:68955260-68955492 | Rare:40 | ||||
| chr17:70169338-70169550 | Common:1; Rare:55 | ||||
| chr17:72120793-72121020 | Rare:57 | ||||
| chr17:73232196-73232709 | Common:3; Rare:188 | ||||
| chr17:74431995-74432095 | Common:1; Rare:46 |