chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116863452368634524CA61GENICpossibly homozygous781688167
116863478768634788GA53GENIChomozygous781688168
116863701368637014CT101GENICheterozygous781688169
116863702368637024AT102GENICheterozygous781688170
116863704968637050TC100GENICheterozygous781688171
116863706768637068TC91GENICheterozygous781688172
116863707068637071TG92GENICheterozygous781688173
116863759168637592CT54GENIChomozygous781688174
116864157868641579AG50GENIChomozygous781688175
116865279668652797GA72GENIChomozygous781688176
116865328768653288GA72GENIChomozygous781688177
116865397368653974CT77GENIChomozygous781688178
116865398268653983CG77GENIChomozygous781688179
116865399068653991CT79GENIChomozygous781688180
116865562068655621AG61GENICpossibly homozygous781688181
116865587468655875AT20GENIChomozygous781688182
116865589268655893GA14GENIChomozygous781688183
116865603868656039AT28GENIChomozygous781688184
116865604568656046GT24GENIChomozygous781688185
116865607968656080GA20GENIChomozygous781688186
116865608568656086GT17GENIChomozygous781688187
116865609768656098CG16GENIChomozygous781688188
116866274368662744TG64GENICpossibly homozygous781688189
116866420368664204CT63GENIChomozygous781688190
116866950168669502CT62GENICheterozygous781688191
116867016268670163CT199GENICheterozygous781688192
116867021368670214TC198GENICheterozygous781688193
116867022268670223CT196GENICheterozygous781688194
116867418468674185GT62GENIChomozygous781688195
116867690268676903TC51GENIChomozygous781688196
116867795668677957CT75GENICpossibly homozygous781688197
116868111468681115GA49GENIChomozygous781688198
116868458968684590AG64GENIChomozygous781688199
116868618468686185AG52GENIChomozygous781688200