chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105548856055488561CT25GENIChomozygous51889964
105548918655489187G-43GENIChomozygous51889967
105549100655491007TC35GENIChomozygous51889969
105549145055491451CT11GENIChomozygous51652993
105549169955491700TC19GENIChomozygous51652995
105549175755491758AG14GENICpossibly homozygous51652997
105549179955491810TGCCATTTTAT-----------7GENIChomozygous51652999
105549186655491867TTCA5GENIChomozygous51889972
105549198755491988AC10GENIChomozygous51889975
105549210355492104CT16GENIChomozygous51653003
105549316055493161A-16GENIChomozygous51653005
105549367555493676CT30GENIChomozygous51653009
105549370755493708TC26GENIChomozygous51889978
105549443255494433TG41GENIChomozygous51459640
105549637855496379GA16GENIChomozygous51653011
105549638055496381GGCACACACACACACACCCACACA9GENIChomozygous52377343
105549729155497292GA29GENIChomozygous51653013
105549748955497490CT6GENIChomozygous51653015
105549777955497780GA4GENIChomozygous51653017
105549782355497824TTG5GENIChomozygous51986538
105549813355498134AC32GENIChomozygous51653023
105549831655498317CT31GENIChomozygous51653025
105549855355498554GA17GENIChomozygous51653027
105549861455498615T-24GENIChomozygous51459644
105549892055498921GA26GENIChomozygous51653029
105549892155498922GA26GENIChomozygous51653031
105549895755498958TC31GENIChomozygous51653032