chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160812356160812357C33GENIChomozygous404434788
5160812356160812357CT33GENICheterozygous404434789
5160812364160812365CA33GENICheterozygous403164627
5160812364160812365C33GENIChomozygous403164628
5160825147160825150ACC14GENIChomozygous141002947
5160860116160860117CT7GENICheterozygous403164640
5160860116160860117C7GENICheterozygous403164641
5160872274160872275A16GENICheterozygous403164644
5160872274160872275AG16GENICheterozygous403164645
5160906062160906063T17GENICheterozygous403601713
5160906062160906063TC17GENICheterozygous403601714
5160906064160906065T22GENICheterozygous403601715
5160906064160906065TC22GENICheterozygous403601716
5160917212160917213CG22GENICheterozygous154251870
5160832063160832064AG57GENIChomozygous137661197
5160917212160917213C22GENICheterozygous403164657
5160917214160917215C22GENICheterozygous403164658
5160917214160917215CG22GENICheterozygous403164659
5160924701160924702T11GENIChomozygous403164662
5160924701160924702TC11GENICheterozygous403164663
5160926841160926842TG6GENICheterozygous137661206
5160956703160956704A29GENICheterozygous403164673
5160956703160956704AG29GENICheterozygous403164674
5160970744160970745TG17GENICheterozygous154252831
5160970744160970745T17GENICheterozygous403164677
5160981142160981143G22GENICheterozygous403164678
5160981142160981143GC22GENICheterozygous403164679
5160986409160986410C13GENICheterozygous403164696
5160986409160986410CT13GENICheterozygous403164697
5161018580161018582TG16GENICheterozygous141002948
5161077772161077773TC49GENIChomozygous137661344
5161078749161078749TTCTTC8GENIChomozygous141002949
5161081137161081138AC15GENIChomozygous154254611
5161081137161081138A15GENICheterozygous403601717
5161084819161084820T9GENICheterozygous137351730