chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2228504640228504641TC2GENIChomozygous624252638
2228504686228504687TC7GENICpossibly homozygous624252639
2228504691228504692T-5GENIChomozygous740472165
2228505272228505273TC11GENIChomozygous624252640
2228505292228505293AAT7GENIChomozygous740472166
2228505606228505607CT13GENIChomozygous624252641
2228505670228505671CT25GENICpossibly homozygous624252642
2228506041228506042TC14GENIChomozygous624252643
2228506325228506326TC13GENICpossibly homozygous624252644
2228506491228506492CT11GENIChomozygous624252645
2228506503228506504CT16GENICpossibly homozygous624252646
2228506548228506549CT11GENIChomozygous624252647
2228506621228506622AG15GENICpossibly homozygous624252648
2228506779228506780GA9GENICheterozygous624252649
2228507182228507183AG11GENIChomozygous624252650
2228507496228507497CG3GENIChomozygous624252651
2228507944228507945CA1GENIChomozygous624252652
2228507947228507948TC2GENICheterozygous624252653
2228508507228508508TA7GENICpossibly homozygous624252654
2228508825228508826GA6GENIChomozygous624252655
2228508827228508828GA7GENIChomozygous624252656
2228508897228508904GGGTTTA-------3GENICheterozygous740472167
2228509255228509256AC15GENIChomozygous624252657
2228509321228509322TA10GENICpossibly homozygous624252658
2228509339228509340TC12GENIChomozygous624252659
2228509520228509521CT22GENICpossibly homozygous624252660
2228509594228509595GA14GENICpossibly homozygous624252661
2228509664228509665CT6GENICheterozygous624252662