chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101300117413001175GA30GENICpossibly homozygous528100314
101300118313001184TTAC24GENIChomozygous692749404
101300165313001654CCTTCT2GENIChomozygous692749406
101300167513001676TC28GENICheterozygous525321054
101300167713001678T-20GENICheterozygous692749407
101300370513003706GGAC24GENIChomozygous692749408
101300380413003805GGA11GENICheterozygous692749410
101300416313004164CT25GENIChomozygous528100315
101300472713004728CT19GENIChomozygous525321055
101300546013005461TC24GENIChomozygous525321056
101300652613006527GGACCA11GENIChomozygous692749411
101300653013006531AG37GENICheterozygous528100316