chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134197078134197079CT10GENIChomozygous955089762
5134197761134197762TA21GENIChomozygous955089763
5134199531134199532TG14GENIChomozygous955089764
5134201404134201405GA18GENIChomozygous955089765
5134202316134202317TG19GENIChomozygous955089766
5134203699134203700CT19GENIChomozygous955089767
5134206183134206184AT35GENICheterozygous955089768
5134206188134206189CT37GENICheterozygous955089769
5134206205134206206GC40GENICheterozygous955089770
5134206206134206207GC41GENICheterozygous955089771
5134206221134206222GA38GENICheterozygous955089772
5134206223134206224AG39GENICheterozygous955089773
5134206332134206333GA20GENICheterozygous955089774
5134206406134206407TG39GENICheterozygous955089775
5134206440134206441GT40GENICheterozygous955089776
5134206476134206477AG36GENICheterozygous955089777
5134206615134206616CT44GENICheterozygous955089778
5134206617134206618GT43GENICheterozygous955089779
5134206707134206708CT33GENICheterozygous955089780
5134206744134206745AG43GENICheterozygous955089781
5134206769134206770GA43GENICheterozygous955089782
5134206790134206791AG41GENICheterozygous955089783