chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71207629712076298TC7GENIChomozygous53790179
71207688012076881GC15GENIChomozygous53790180
71207689512076896GC14GENIChomozygous53790181
71207690012076901TC13GENIChomozygous53790182
71207718212077183GGT9GENICpossibly homozygous56141855
71207737912077380CG7GENIChomozygous53790183
71207769312077694CT8GENIChomozygous56141858
71207786812077869TC4GENIChomozygous53790184
71207808612078091TTTTT-----2GENICheterozygous54954752
71207869112078692GA4GENIChomozygous56141861
71207893812078939TC5GENIChomozygous53790189
71208163412081635AG6GENIChomozygous53790193
71208186912081870AG4GENIChomozygous53790194
71208281912082820AG3GENIChomozygous56141864
71208290512082906TG4GENIChomozygous53790195
71208513712085138TG12GENIChomozygous56141867
71208579812085800TT--4GENICheterozygous54954754
71208603312086068CTCCTAGGCATCTGAGTTCTCAGCCATCAGTATGA-----------------------------------3GENIChomozygous56141870
71208579712085800TTT---4GENICheterozygous55057491