chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116823142116823143TC19GENIChomozygous597090441
7116823343116823344T-2GENIChomozygous727204241
7116823521116823522TC17GENICpossibly homozygous597090442
7116824211116824212TC20GENICheterozygous597090443
7116825093116825094GA12GENIChomozygous597090444
7116825103116825104GA11GENIChomozygous597090445
7116825628116825629AT23GENICpossibly homozygous597090446
7116826213116826214CCA3GENICheterozygous727204243
7116826543116826544AG23GENIChomozygous597090447
7116826982116826983GA32GENICpossibly homozygous597090448
7116828351116828352GT7GENICheterozygous597090449
7116829856116829857GT25GENICpossibly homozygous597090450
7116832075116832076CCCTG5GENIChomozygous727204244
7116832310116832311TG27GENICpossibly homozygous597090451
7116833888116833889TC29GENICpossibly homozygous597090452
7116834093116834094AG15GENICpossibly homozygous597090453
7116834099116834100TA17GENICpossibly homozygous597605241
7116834100116834101CA18GENICpossibly homozygous597605242
7116834256116834257A-27GENICpossibly homozygous727204245
7116834291116834292CA21GENICheterozygous597090454
7116834292116834293TG21GENICheterozygous597090455