chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121011997210119973AC5GENICheterozygous50041799
121017007710170078TC17GENICheterozygous50041956
121017384710173848CT14GENICheterozygous50041992
121017588410175885TC40GENICheterozygous50042022
121018553910185540GA16GENICheterozygous50042090
121018555610185557AG23GENICheterozygous50042092
121018570410185705CT42GENICheterozygous50042094
121018619410186195GA5GENICheterozygous50042124
121018622110186222GA5GENICheterozygous50042126
121018831710188318CT6GENICheterozygous50042188
121018834610188347TC13GENICheterozygous50042190
121018844010188441AG17GENICheterozygous50042192
121018849210188493TC13GENICheterozygous50042194
121018850310188504GA14GENICheterozygous50042196
121018873310188734GA18GENICheterozygous50042198
121018878810188789TC19GENICheterozygous50042200
121018886810188869CT17GENICheterozygous50042202
121018893110188932AG15GENICheterozygous50042204
121018894910188950GA14GENICheterozygous50042206
121018895610188957AG16GENICheterozygous50042208
121018896110188962CT16GENICheterozygous50042210
121018901410189015G-12GENICheterozygous50042212
121018917510189176GT14GENICheterozygous50042214
121018917610189177GC14GENICheterozygous50042216
121018919810189199AT15GENICheterozygous50042218
121018929510189296CT35GENICheterozygous50042220
121018934310189344CA31GENICheterozygous50042222
121018936710189368GA32GENICheterozygous50042224
121018937510189376TC31GENICheterozygous50042226
121018950610189507CT27GENICheterozygous50042228
121018966110189662CT21GENICheterozygous50042230
121019004810190049TC37GENICheterozygous50042232
121019024410190245AG25GENICheterozygous50042238
121019068710190688CT52GENICheterozygous50042240
121019089610190897AG47GENICheterozygous50042242
121019135210191353CT32GENICheterozygous50042246
121019224410192245GA57GENICheterozygous50042248
121019239410192395AG42GENICheterozygous50042250
121019254010192541AG34GENICheterozygous50042252