chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1117909010117909011CT9GENIChomozygous575197477
1117909079117909080AG1GENIChomozygous575197478
1117909081117909082GA1GENIChomozygous575197479
1117909444117909445TTG2GENICheterozygous712789336
1117909448117909449G-2GENICheterozygous712789337
1117909608117909609GT48GENIChomozygous573039062
1117909700117909701CCA34GENIChomozygous712789338
1117910380117910381GC31GENICheterozygous573039063
1117910514117910516AT--7GENIChomozygous712789339
1117910521117910522GGTC4GENIChomozygous712789340
1117910522117910523GGA4GENIChomozygous712789341
1117910676117910677G-6GENICheterozygous712789342
1117910715117910716CG6GENICheterozygous575197480
1117910718117910719CT5GENICheterozygous575197481
1117910719117910720CT5GENICheterozygous575197482
1117910719117910720CA5GENICheterozygous575197483
1117910722117910723CG5GENIChomozygous573039064
1117910730117910731T-4GENICheterozygous712789343
1117910735117910736AG3GENIChomozygous575197484
1117910935117910936G-32GENICheterozygous712789344
1117911018117911019CCT33GENIChomozygous712789345