chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171867864171867865TC23GENIChomozygous60944003
1171868343171868344AG27GENICpossibly homozygous60944004
1171868379171868380CT29GENICpossibly homozygous60944005
1171869399171869400TC29GENICpossibly homozygous60944006
1171869614171869615GC18GENIChomozygous60944007
1171870455171870456TC22GENICpossibly homozygous60944008
1171870910171870911TC20GENICpossibly homozygous60944009
1171871053171871054AG25GENIChomozygous60944010
1171871426171871427CT20GENICpossibly homozygous60944011
1171871793171871794CT15GENIChomozygous60944012
1171872250171872251GA17GENIChomozygous60944013
1171872814171872815CT28GENIChomozygous60944014
1171873229171873230CT4GENIChomozygous60944015
1171873512171873513TC31GENICpossibly homozygous60944016
1171873831171873832CT25GENIChomozygous60944017
1171873979171873980GA15GENICpossibly homozygous60944018
1171874454171874455GA3GENIChomozygous60944019
1171875022171875023CT29GENICpossibly homozygous60944020
1171875333171875334TC16GENICpossibly homozygous60944021
1171875436171875437CT14GENIChomozygous60944022
1171875478171875479TC20GENIChomozygous60944023
1171875760171875761AC17GENICpossibly homozygous60944024
1171877171171877172GA28GENIChomozygous60944025
1171877208171877209TC28GENIChomozygous60944026
1171877735171877736AG11GENIChomozygous60944027
1171877936171877937CT14GENICpossibly homozygous60944030
1171878199171878200AG20GENIChomozygous60944031
1171879454171879455GA22GENICpossibly homozygous60944033
1171881369171881370CT14GENIChomozygous60944034
1171881567171881568AG16GENIChomozygous60944035
1171882823171882824GGA2GENICheterozygous60944037
1171883032171883033CT9GENIChomozygous60944038
1171884241171884242GA9GENIChomozygous60944039
1171884259171884260AC5GENIChomozygous60944040
1171884278171884279AG13GENIChomozygous60944041
1171884511171884512TA29GENICpossibly homozygous60944042