chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161437123414371235GA20GENIChomozygous111733136
161437131614371317GA18GENICheterozygous111939967
161437313714373138AG22GENIChomozygous111733138
161437324414373245TC27GENIChomozygous111733140
161437443914374440CT19GENIChomozygous111733142
161437457214374573CA24GENICpossibly homozygous111733144
161437635914376360AG39GENIChomozygous111733146
161437639514376396AC36GENIChomozygous111733148
161437653614376537CT28GENICpossibly homozygous111733150
161437673014376731TA29GENIChomozygous111733152
161437682114376822AG29GENIChomozygous111733154
161437684714376848CT21GENIChomozygous111733156
161437698614376987CT37GENIChomozygous111733158
161437702114377022AG35GENIChomozygous111733160
161437718414377185CT39GENIChomozygous111733162
161437769114377692CA28GENIChomozygous111733164
161437790014377901CT24GENIChomozygous111733166
161437866514378666CA28GENIChomozygous111733168
161437911614379117GA33GENIChomozygous111733170
161437924314379244GA29GENIChomozygous111733173
161437933214379333CT22GENIChomozygous111733175
161437934114379342AT20GENIChomozygous111733177
161437936514379366CA21GENIChomozygous111733179
161437937114379372CT22GENIChomozygous111733181
161437938314379384CT21GENIChomozygous111733183
161437941914379420CG23GENIChomozygous111733185
161437943714379438CA23GENIChomozygous111733187
161437950914379510GA31GENIChomozygous111733189
161438010714380108TC20GENIChomozygous111733191
161438038914380390CA26GENIChomozygous111733193
161438042614380427TC26GENIChomozygous111733195
161438085014380851AG36GENIChomozygous111733197
161438090614380907TA40GENIChomozygous111733199
161438125014381251CT27GENIChomozygous111733201
161438140014381401TA17GENIChomozygous111733203
161438155614381557TG24GENIChomozygous111733205
161438156214381563CG23GENIChomozygous111733207
161438183514381836GT28GENIChomozygous111733209
161438185114381852CT28GENIChomozygous111733211