chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101300062813000629CT30GENIChomozygous610314745
101300118313001184TTAC19GENICpossibly homozygous734033899
101300118413001186AC--19GENICheterozygous734033898
101300124913001251CA--13GENIChomozygous734033900
101300165413001678TTCTTTCTTTCTTTCTTTCTTTCT------------------------13GENIChomozygous734033903
101300380413003805GGAA9GENICpossibly homozygous734033906
101300396013003961AATT9GENICpossibly homozygous734033907
101300429613004297TTCTCTCTCACACA21GENICheterozygous734033908
101300472713004728CT21GENIChomozygous610314746
101300544613005447CT25GENIChomozygous612358659
101300546013005461TC28GENIChomozygous610314747
101300652613006527GGACCAACCAACCA5GENIChomozygous734033913
101300741113007412TC26GENIChomozygous612358660