chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
25096638350966384AC41GENIChomozygous58817781
25096652150966522TTAC8GENIChomozygous59689470
25096656750966568TG28GENIChomozygous58817783
25096676750966768CA26GENIChomozygous60209667
25096692050966921CA44GENIChomozygous59689472
25096699850966999A-20GENIChomozygous60209668
25096964450969645TA27GENIChomozygous60209669
25096978450969785AG21GENIChomozygous58817791
25096991650969917AG13GENIChomozygous58817792
25096996550969966A-22GENIChomozygous60112351
25097006850970069G-22GENIChomozygous58817793
25097076750970768GGA12GENIChomozygous60209670
25097078550970787AT--12GENICpossibly homozygous58817795
25097114650971147CT34GENIChomozygous60209671
25097178950971790GT17GENIChomozygous60209672
25097217750972178AT31GENICpossibly homozygous60209673
25097399750974000GGA---14GENIChomozygous58817807
25097419950974200TC25GENICpossibly homozygous60209674
25097422550974226AG23GENIChomozygous58817809
25097396650973982GAAAGAGGGAGGGAGG----------------18GENIChomozygous60566680
25096947650969477CCCACACACA6GENIChomozygous60479532
25097438150974382AAGG20GENICheterozygous60209675
25097438150974382AAG20GENICpossibly homozygous60566681