chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5124701935124701936AG22GENIChomozygous504044107
5124701985124701986TC18GENIChomozygous501836183
5124701992124701993CT18GENIChomozygous504044108
5124701998124702003AAAAA-----9GENIChomozygous683972186
5124702109124702110CA52GENIChomozygous504044109
5124702262124702263CA37GENIChomozygous501836184
5124702395124702396GC28GENIChomozygous501836185
5124702480124702481GC21GENIChomozygous501836186
5124702548124702549CCT27GENIChomozygous683972187
5124702611124702612TC41GENIChomozygous501836187
5124702961124702962TC31GENIChomozygous504044110
5124703055124703056GA36GENICheterozygous504044111
5124703092124703093GA59GENICheterozygous504044112
5124703118124703119GT73GENICheterozygous504044113
5124703138124703139CA89GENICheterozygous504044114
5124703141124703142CT95GENICheterozygous504044115
5124703147124703148GA104GENICheterozygous504044116
5124703167124703168AC124GENICheterozygous504044117
5124703201124703202GA156GENICheterozygous504044118
5124703270124703271GA130GENICheterozygous504044119
5124703298124703299GA108GENICheterozygous504044120
5124703324124703325AG80GENICheterozygous504044121
5124703328124703329TG74GENICheterozygous504044122
5124703355124703356AC70GENIChomozygous501836188
5124703365124703366AC65GENICheterozygous504044123
5124703378124703379TG54GENICheterozygous504044124
5124703433124703434CT40GENICpossibly homozygous501836189
5124703520124703521CG56GENIChomozygous501836190
5124703596124703597AC53GENIChomozygous501836191
5124703675124703676CA51GENICpossibly homozygous501836192
5124703741124703742TC42GENIChomozygous501836193
5124703993124703994TC53GENIChomozygous501836194