chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116823142116823143TC20GENICpossibly homozygous631465261
7116823343116823344T-3GENICheterozygous745667892
7116823521116823522TC14GENIChomozygous631465262
7116824211116824212TC17GENICpossibly homozygous631465263
7116825093116825094GA14GENICpossibly homozygous631465264
7116825103116825104GA12GENIChomozygous631465265
7116825628116825629AT14GENIChomozygous631465266
7116825974116825975TTA6GENICheterozygous745667893
7116826543116826544AG11GENIChomozygous631465267
7116826982116826983GA14GENIChomozygous631465268
7116828351116828352GT7GENICpossibly homozygous631465269
7116829856116829857GT15GENIChomozygous631465270
7116832075116832076CCCTG1GENIChomozygous745667894
7116832310116832311TG21GENICpossibly homozygous631465271
7116832608116832611AAA---2GENIChomozygous745667895
7116833048116833049CCT1GENIChomozygous745667898
7116833888116833889TC18GENICpossibly homozygous631465272
7116834093116834094AG8GENIChomozygous631465273
7116834099116834100TA9GENIChomozygous631465274
7116834100116834101CA9GENIChomozygous631465275
7116834256116834257A-12GENICpossibly homozygous745667899
7116834291116834292CA17GENICheterozygous631465276
7116834292116834293TG17GENICheterozygous631465277