chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124871898748718988GT5GENIChomozygous50229013
124871899148718992AG2GENIChomozygous50229015
124871987348719874GGGAGAGAGAGAGAGAGAGAGAGAGA1GENIChomozygous50575499
124872034248720343AG5GENIChomozygous50229017
124872134348721344CCCCTCCCTCCCTT1GENIChomozygous50513636
124872215448722155TC17GENICpossibly homozygous50229025
124872256648722567AT12GENIChomozygous50229027
124872270948722710CT17GENICpossibly homozygous50229029
124872447948724480TTA15GENIChomozygous50229035
124872466048724661AG7GENIChomozygous50229037
124872475848724762AGGG----4GENIChomozygous50229039
124872488048724881CT13GENICpossibly homozygous50229041
124872539048725391TC15GENIChomozygous50229043
124872632348726324AG12GENIChomozygous50229049
124872671948726720AG15GENICpossibly homozygous50229051
124872697548726976CT10GENICheterozygous50229053
124872699848726999GA13GENICpossibly homozygous50229055
124872703648727037TC20GENIChomozygous50229057