chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4144204903144204904AG36GENIChomozygous56964165
4144205353144205354CT44GENIChomozygous59643752
4144205800144205801AC65GENIChomozygous56964168
4144205923144205924CT37GENIChomozygous56964169
4144205934144205935GA37GENIChomozygous59643754
4144206050144206051A-26GENIChomozygous56964170
4144208472144208482ACACACACAC----------6GENICheterozygous59643756
4144210725144210726AG33GENIChomozygous56964180
4144211252144211253GT30GENIChomozygous59643758
4144211329144211330GGTA17GENICpossibly homozygous59130116
4144211806144211807AT30GENIChomozygous59643760
4144212437144212438CT21GENIChomozygous59643762
4144208119144208120CT38GENIChomozygous59314393
4144211933144211934GGCACACACACACACACACACACA12GENIChomozygous58343422
4144210026144210032ACACAC------12GENICheterozygous59059537