chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2140547129140547130TG15GENIChomozygous75822724
2140547130140547131GC14GENIChomozygous75822726
2140547178140547179TC11GENICpossibly homozygous73959966
2140547180140547181TC12GENICheterozygous73959967
2140547183140547184AT14GENICheterozygous73959968
2140547228140547229GA16GENICheterozygous78679737
2140547236140547237AG14GENICheterozygous73959969
2140547977140547978GC42GENIChomozygous73959970
2140548496140548497TC14GENIChomozygous73959971
2140552446140552447CT22GENIChomozygous73959972
2140552447140552448CG22GENIChomozygous73959973
2140558784140558785TC32GENIChomozygous73959976
2140559142140559143CG31GENIChomozygous73959977
2140559265140559266CT20GENIChomozygous73959978
2140559561140559562GT8GENIChomozygous73959979
2140559695140559696AC12GENICheterozygous73959980
2140559697140559698GT13GENICheterozygous73959981
2140559752140559753TC23GENICheterozygous73959983
2140559753140559754GA23GENICheterozygous73959984
2140559757140559758CT22GENICheterozygous73959985
2140559895140559896CT24GENICpossibly homozygous73959986
2140560233140560234TC26GENIChomozygous73959987
2140560592140560593GT23GENIChomozygous73959988
2140561035140561036GA28GENIChomozygous73959989
2140561712140561713CT28GENIChomozygous73959990
2140562233140562234AC21GENIChomozygous73959991
2140563317140563318GA16GENIChomozygous73959992
2140564136140564137GA26GENIChomozygous73959993
2140565484140565485AT23GENIChomozygous73959995
2140565485140565486CT24GENIChomozygous73959996
2140565976140565977TC24GENIChomozygous73959997
2140567262140567263TC27GENIChomozygous75244144
2140568255140568256TC27GENIChomozygous73959998