chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123745800537458006TC2GENIChomozygous115704184
123745905437459055AG5GENIChomozygous115380990
123746157837461579AG9GENIChomozygous115320436
123746183337461834GA12GENIChomozygous115475736
123746218637462187CT4GENIChomozygous115475738
123746282837462829AG6GENIChomozygous115320446
123746293637462937AT6GENIChomozygous115320448
123746335037463351TC12GENIChomozygous115380992
123746337437463375AC10GENIChomozygous115380994
123746388637463887AC9GENICpossibly homozygous115380998
123746438737464388CT3GENIChomozygous115381006
123746442337464424CT3GENIChomozygous115381008
123746450437464505AG7GENIChomozygous115381010
123746450737464508AG8GENIChomozygous115381012
123746460537464606GA5GENIChomozygous115381014
123746462937464630GA5GENIChomozygous115493835
123746472337464724TA4GENIChomozygous115381016
123746472637464727CA4GENIChomozygous115381018
123746475837464759GA5GENIChomozygous115475740
123746477437464775GA6GENIChomozygous115320452
123746481737464818GA5GENIChomozygous115381020
123746484337464844CA5GENIChomozygous115381022
123746485537464856TA5GENIChomozygous115381024
123746500237465003AC6GENIChomozygous115381028
123746500537465006CT6GENIChomozygous115381030
123746542637465427CG9GENIChomozygous115475742
123746580437465805CT12GENIChomozygous115475744
123746629537466296GA7GENIChomozygous115475746
123746763937467640AT4GENIChomozygous115475748