chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9119307398119307399AT14GENICheterozygous126534707
9119307469119307470CG9GENICheterozygous126613261
9119307940119307941TC12GENIChomozygous117653185
9119309769119309770TC11GENIChomozygous117653186
9119310000119310001AG13GENIChomozygous117653187
9119310338119310339TA15GENIChomozygous117653188
9119310574119310575TC13GENIChomozygous117653189
9119311324119311325AG10GENIChomozygous117653191
9119312406119312407GA15GENIChomozygous117743881
9119310083119310084CT13GENIChomozygous117743877
9119311523119311524GA9GENIChomozygous117743879
9119310931119310932CT9GENIChomozygous117778877
9119312604119312605CT13GENIChomozygous117653192
9119312906119312907GA16GENIChomozygous117445232
9119313114119313115TC11GENIChomozygous117743883
9119313210119313211TC16GENIChomozygous117653193
9119313366119313367TC8GENIChomozygous117653194
9119313651119313652GA11GENIChomozygous117653195
9119313770119313771TC9GENIChomozygous117653196
9119314820119314821CT10GENIChomozygous117653201
9119315230119315231CT15GENIChomozygous117653202
9119316171119316172TC12GENIChomozygous117653203
9119318475119318476AT18GENIChomozygous117653204
9119319358119319359AG14GENIChomozygous117653205
9119320114119320115AC4GENICheterozygous117653206
9119320462119320463CA20GENIChomozygous117653207
9119320815119320816TC15GENIChomozygous117653208