chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83149982331499824GT24GENIChomozygous116446849
83149982631499827CT24GENIChomozygous117101669
83149991331499914TG19GENIChomozygous116446850
83150035431500355CT23GENIChomozygous117101670
83150316331503164AC26GENIChomozygous117101671
83150343331503434TG25GENIChomozygous116446855
83150356631503567AG26GENIChomozygous116446856
83150667331506674CT26GENIChomozygous116788770
83150722831507229GA20GENIChomozygous117101672
83150840031508401TA27GENIChomozygous116446863
83150945531509456GA30GENIChomozygous117101673
83150531831505322CTCC8GENIChomozygous128579022
83150528631505287CG11GENIChomozygous118089805
83150529031505291CG12GENICpossibly homozygous131058363
83151220031512201TC31GENIChomozygous116446866
83151468831514689GA35GENIChomozygous116446870
83151588331515884GA26GENIChomozygous117101674
83151658831516589AG21GENIChomozygous116788772
83151780131517802TC37GENIChomozygous116446878
83152026731520268GA15GENIChomozygous117101675
83152111831521119GT20GENIChomozygous116446884
83152112531521126C21GENIChomozygous128579026
83152291531522916CT10GENIChomozygous126663150
83152353131523532CT11GENIChomozygous116446885
83152741631527417GA34GENIChomozygous117101680
83152744631527447AC35GENIChomozygous116446891
83152790231527903GT29GENIChomozygous117101681
83152822231528223TC33GENIChomozygous116446892
83152892831528929TC28GENIChomozygous116446893
83152997331529974AT35GENIChomozygous116446894
83153050431530505AG22GENIChomozygous117101682
83153197531531976TG35GENIChomozygous116446897
83153251031532511AG20GENIChomozygous117101683
83153273631532737TC31GENIChomozygous116446899
83153326231533263AG19GENIChomozygous117101684
83151653731516537CAGGTGTGCACTGCCAGTGAAGGAA23GENIChomozygous132121391