chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161094344210943443T-20INTERGENIChomozygous47729316
161094368910943690CG32INTERGENIChomozygous47729318
161094465310944654AG19INTERGENIChomozygous47273108
161094612910946130GT30INTERGENIChomozygous47729320
161094711610947117TC19INTERGENIChomozygous47273116
161094878110948782CT13INTERGENIChomozygous47729322
161095011210950114TT--26INTERGENIChomozygous47273127
161095044310950444CT15INTERGENIChomozygous47729324
161095139810951399AG29INTERGENIChomozygous47273131
161095362110953622CT20INTERGENIChomozygous47729328
161096006110960062GGT11INTERGENIChomozygous47729332
161096053910960540TC15INTERGENIChomozygous47273167
161096142510961426GT15INTERGENIChomozygous47729334
161096164010961641CT30INTERGENIChomozygous47729336
161096202110962022AAT29INTERGENIChomozygous47729338
161096401210964013CT27INTERGENIChomozygous47729340
161096426710964268TC23INTERGENIChomozygous47273183
161096449010964491AG23INTERGENIChomozygous47273187
161096505310965054CT28INTERGENICpossibly homozygous47729342
161096585310965854TC27INTERGENIChomozygous47273213
161094739010947394GTGT----15INTERGENICheterozygous47834938
161094739210947394GT--15INTERGENICheterozygous48053443
161096507010965071CG29INTERGENICpossibly homozygous48137177