| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:64532746-64532871 | Rare:30 | ||||
| chr17:65056549-65056955 | Common:4; Rare:168 | ||||
| chr17:67366470-67366965 | Rare:125 | ||||
| chr17:67717696-67717971 | Rare:94 | ||||
| chr17:68247813-68248142 | Common:6; Rare:145 | ||||
| chr17:68259101-68259205 | Rare:36 | ||||
| chr17:68525518-68525892 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr17:70169344-70169550 | Common:1; Rare:53 | ||||
| chr17:73232243-73232708 | Common:3; Rare:165 | ||||
| chr17:74431285-74431390 | Rare:27 | ||||
| chr17:74431874-74432141 | Common:1; Rare:99 | ||||
| chr17:74432399-74432503 | Common:1; Rare:23 | ||||
| chr17:74776281-74776506 | Common:4; Rare:71 | ||||
| chr17:75012546-75012689 | Common:1; Rare:35 | ||||
| chr17:75046929-75047211 | Common:1; Rare:86 |