chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1219000943219000944GC26GENIChomozygous109367698
1219002652219002653TA22GENIChomozygous109367699
1219002893219002894CG27GENIChomozygous109367700
1219003121219003122GA26GENIChomozygous108540034
1219004730219004731GC12GENIChomozygous109367701
1219005311219005312TC33GENIChomozygous108540036
1219006137219006138TG32GENIChomozygous109367702
1219007358219007359TC14GENIChomozygous108540040
1219008046219008047TC25GENIChomozygous108540042
1219010153219010154TC4GENIChomozygous108540044
1219010775219010776AG26GENIChomozygous108540046
1219013678219013679CT23GENIChomozygous108993801
1219014181219014182AG32GENIChomozygous108540052
1219014841219014842GA35GENIChomozygous108993802
1219016898219016899CA27GENIChomozygous108540054
1219021331219021332GC35GENICheterozygous108540060
1219021335219021336GC35GENICheterozygous108540062
1219021366219021367AG30GENIChomozygous109367703
1219022426219022427CT41GENICheterozygous109367704
1219024812219024813GT17GENICpossibly homozygous108540068
1219026088219026089TC16GENIChomozygous108540072
1219026787219026788GA34GENICpossibly homozygous108540074
1219027538219027539CA11GENIChomozygous108540076
1219030837219030838AT41GENICheterozygous109367705
1219031340219031341AG33GENIChomozygous108540078
1219031833219031834CT21GENIChomozygous109367706
1219033095219033096GC15GENIChomozygous108540082
1219033367219033368GA30GENIChomozygous108993803
1219036556219036557GA25GENIChomozygous108540084
1219037120219037121AG11GENIChomozygous108993805
1219037762219037763AC29GENIChomozygous108540086
1219038065219038066AT34GENIChomozygous108540088
1219040526219040527AG33GENIChomozygous108540090
1219040723219040724AG26GENIChomozygous108540092
1219041923219041924GC34GENIChomozygous108993809
1219042635219042636TG18GENIChomozygous108540094
1219044114219044115TC37GENIChomozygous108993810
1219044308219044309AG24GENIChomozygous108993811
1219045657219045658AG22GENIChomozygous108540100