chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186227907162279072AG19GENIChomozygous787525164
186227928462279285CT22GENIChomozygous787525165
186227939462279395AG19GENIChomozygous787525166
186227943562279436CT23GENIChomozygous787525167
186227944662279447CT21GENIChomozygous787525168
186227954462279545TC7GENIChomozygous787525169
186227958962279590AG13GENIChomozygous787525170
186227960862279609CA15GENIChomozygous787525171
186227962962279630GA17GENIChomozygous787525172
186227967662279677TC19GENIChomozygous787525173
186227971562279716TC17GENIChomozygous787525174
186228039162280392CT11GENICpossibly homozygous787525175
186228048362280484CA17GENIChomozygous787525176
186228055362280554TA15GENIChomozygous787525177
186228060362280604CT13GENIChomozygous787525178
186228074362280744CT19GENIChomozygous787525179
186228079562280796TC15GENIChomozygous787525180
186228080162280802AG13GENIChomozygous787525181
186228082462280825TC17GENIChomozygous787525182
186228089062280891TC19GENIChomozygous787525183
186228105962281060GC21GENIChomozygous787525184
186228133462281335CT23GENIChomozygous787525185
186228160862281609AT27GENIChomozygous787525186
186228222262282223TC13GENIChomozygous787525187
186228226062282261AG12GENICheterozygous787525188
186228228662282287TC12GENICpossibly homozygous787525189
186228232162282322TC10GENICpossibly homozygous787525190
186228235762282358CT21GENICheterozygous787525191
186228264262282643CT19GENICpossibly homozygous787525192
186228264362282644AG19GENIChomozygous787525193
186228266562282666TC18GENICpossibly homozygous787525194
186228278962282790CA12GENIChomozygous787525195
186228280462282805AG14GENIChomozygous787525196
186228288962282890CT74GENICheterozygous787525197
186228304562283046AT70GENICheterozygous787525198
186228711162287112TA14GENIChomozygous787525199
186228727462287275AG23GENIChomozygous787525200
186228730062287301TC24GENIChomozygous787525201
186228735662287357CT23GENIChomozygous787525202