chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117223808972238090CT17GENICheterozygous50825132
117224259472242595AG16GENICheterozygous50825153
117225385772253858GT23GENICheterozygous50825264
117226381772263818AG13GENICheterozygous50825348
117226398172263982TC17GENICheterozygous50825352
117226401272264013TC14GENICheterozygous50825354
117232413872324139TC28GENICheterozygous50826037
117234061072340611TC29GENICheterozygous50826171
117234072572340726GT20GENICheterozygous50826173
117234078772340788TC15GENICheterozygous50826175
117234079272340793AG12GENICheterozygous50826177
117236741372367414T-30INTERGENICheterozygous50826381
117236748572367486AG25INTERGENICheterozygous50826383
117237400972374010GA8GENICheterozygous50826452
117237420972374210AG15GENICheterozygous50826454
117237433172374332CT13GENICheterozygous50826456
117237474672374747CT27GENICheterozygous50826458
117237610172376102CT12GENICheterozygous50826466
117237622272376223AG25GENICheterozygous50826468
117237642672376427CT9GENICheterozygous50826470