chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124345841124345842TA5GENICheterozygous877271538
7124345843124345844TA5GENICheterozygous877271537
7124346015124346016TC16GENIChomozygous877271536
7124346975124346976AG11GENIChomozygous877271535
7124347454124347455GA22GENIChomozygous877271534
7124349087124349088AC26GENIChomozygous877271533
7124351263124351264TC4GENIChomozygous877271532
7124354042124354043AG5GENIChomozygous877271531
7124354541124354542AG23GENIChomozygous877271530
7124357260124357261GA18GENIChomozygous877271529
7124357588124357589GA16GENIChomozygous877271528
7124357875124357876GA11GENIChomozygous877271527
7124358195124358196GA25GENIChomozygous877271526
7124359640124359641GA20GENIChomozygous877271525
7124360476124360477CT12GENIChomozygous877271524
7124362633124362634GA26GENIChomozygous877271523
7124363341124363342CA27GENIChomozygous877271522
7124364483124364484CT8GENIChomozygous877271521
7124366143124366144AG19GENIChomozygous877271520
7124366322124366323GA29GENIChomozygous877271519
7124367434124367435GT23GENIChomozygous877271518