chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105548856055488561CT36GENIChomozygous51889964
105548918655489187G-34GENIChomozygous51889967
105549100655491007TC23GENIChomozygous51889969
105549145055491451CT29GENIChomozygous51652993
105549169955491700TC22GENIChomozygous51652995
105549175755491758AG21GENIChomozygous51652997
105549179955491810TGCCATTTTAT-----------23GENIChomozygous51652999
105549186655491867TTCA23GENICpossibly homozygous51889972
105549198755491988AC24GENIChomozygous51889975
105549210355492104CT22GENIChomozygous51653003
105549316055493161A-21GENIChomozygous51653005
105549367555493676CT47GENIChomozygous51653009
105549370755493708TC47GENIChomozygous51889978
105549443255494433TG39GENIChomozygous51459640
105549637855496379GA25GENIChomozygous51653011
105549638055496381GGCACACACACACACACCCACACA20GENIChomozygous52377343
105549729155497292GA20GENIChomozygous51653013
105549748955497490CT15GENIChomozygous51653015
105549777955497780GA4GENIChomozygous51653017
105549782355497824TTG3GENIChomozygous51986538
105549813355498134AC42GENIChomozygous51653023
105549831655498317CT41GENIChomozygous51653025
105549855355498554GA33GENIChomozygous51653027
105549861455498615T-45GENIChomozygous51459644
105549892055498921GA29GENIChomozygous51653029
105549892155498922GA29GENIChomozygous51653031
105549895755498958TC34GENIChomozygous51653032