chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2140547129140547130TG5GENIChomozygous75822724
2140547130140547131GC5GENIChomozygous75822726
2140547178140547179TC4GENIChomozygous73959966
2140547180140547181TC4GENIChomozygous73959967
2140547183140547184AT7GENIChomozygous73959968
2140547612140547613TC20GENIChomozygous75244128
2140548496140548497TC21GENIChomozygous73959971
2140549533140549534GT26GENIChomozygous75244130
2140549869140549870GA22GENIChomozygous75244132
2140552446140552447CT31GENIChomozygous73959972
2140552447140552448CG31GENIChomozygous73959973
2140555242140555243GT28GENIChomozygous75244134
2140558537140558538CT20GENIChomozygous75244136
2140558784140558785TC30GENIChomozygous73959976
2140559142140559143CG14GENIChomozygous73959977
2140559265140559266CT17GENIChomozygous73959978
2140559561140559562GT8GENIChomozygous73959979
2140559695140559696AC5GENICheterozygous73959980
2140559697140559698GT5GENICheterozygous73959981
2140559752140559753TC15GENICpossibly homozygous73959983
2140559753140559754GA15GENICpossibly homozygous73959984
2140559757140559758CT14GENICpossibly homozygous73959985
2140559895140559896CT25GENICpossibly homozygous73959986
2140560233140560234TC19GENIChomozygous73959987
2140560592140560593GT18GENIChomozygous73959988
2140561035140561036GA22GENIChomozygous73959989
2140562233140562234AC12GENIChomozygous73959991
2140562886140562887TA23GENIChomozygous75244138
2140563317140563318GA21GENIChomozygous73959992
2140565976140565977TC26GENIChomozygous73959997
2140566224140566225GA25GENIChomozygous75244142
2140567262140567263TC23GENICheterozygous75244144