chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1114043262114043264AG--2GENIChomozygous60804286
1114043291114043292GT8GENICheterozygous60804287
1114060000114060001G-5GENIChomozygous60804296
1114064163114064164CCA12GENIChomozygous60804315
1114064737114064738AT3GENICheterozygous60804318
1114104229114104230C-1GENIChomozygous60804445
1114106744114106745A-6GENIChomozygous60804447
1114106761114106762G-4GENIChomozygous60804448
1114106783114106784GT1GENIChomozygous60804449
1114108753114108754CT9GENICpossibly homozygous60804453
1114108768114108769CT7GENICheterozygous60804454
1114108769114108770CT7GENICheterozygous60804455
1114109457114109458AAG3GENIChomozygous60804456
1114109458114109459TA3GENIChomozygous62086157
1114109486114109487TA1GENIChomozygous60804457
1114125150114125151T-7GENICheterozygous61956451
1114150400114150401AG9GENICheterozygous60804563
1114170826114170827C-17GENIChomozygous60804626
1114176809114176810C-1GENIChomozygous62294154
1114253772114253887CTTCTTTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTAGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCC-------------------------------------------------------------------------------------------------------------------7GENIChomozygous62086169
1114255254114255255TG12GENICheterozygous61744253