chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228264664228264667GGC---24GENIChomozygous61106912
1228265074228265075AG27GENIChomozygous61106913
1228265567228265568CG26GENIChomozygous61106914
1228265940228265941TC23GENIChomozygous61106915
1228266157228266159TT--22GENICheterozygous61603466
1228266158228266159T-22GENICpossibly homozygous61603467
1228266176228266177TC27GENICpossibly homozygous61106917
1228266357228266358AC24GENIChomozygous61106918
1228266532228266533AG31GENIChomozygous61106919
1228267209228267210G-2GENIChomozygous61106920
1228267446228267447T-15GENIChomozygous61106921
1228267969228267970TC13GENICpossibly homozygous61106923
1228268107228268109TT--3GENIChomozygous61683222
1228268129228268130GT10GENICpossibly homozygous61106924
1228268788228268796TCCTTCCC--------8GENICheterozygous61106928
1228268795228268796CT12GENICheterozygous61106929
1228268955228268956CT36GENIChomozygous61603468
1228271086228271087TTTG17GENIChomozygous61106932
1228271104228271105AG24GENIChomozygous61106934
1228271241228271242T-11GENICheterozygous61106935
1228271244228271245G-9GENICheterozygous61106936
1228271368228271370TG--3GENIChomozygous61106937
1228271396228271397AG1GENIChomozygous61106938
1228273207228273208CA6GENIChomozygous61106939
1228273239228273240GA11GENIChomozygous61106940
1228273704228273705TC29GENIChomozygous61106941
1228273898228273899AG30GENIChomozygous61106942
1228274276228274277AAT19GENIChomozygous61967706
1228274338228274339CT30GENIChomozygous61967707
1228274438228274439GA32GENIChomozygous61967708
1228274519228274520CT32GENIChomozygous61967709
1228274969228274970GA24GENICpossibly homozygous61967710
1228275967228275968TC27GENIChomozygous61106947
1228276286228276287CA23GENIChomozygous61106948
1228276957228276958CT25GENIChomozygous61106949
1228277831228277832A-31GENIChomozygous61603481
1228277844228277845CG32GENIChomozygous61603483