chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134746028947460290CT54GENIChomozygous139289166
134746030947460309A48GENIChomozygous139171929
134746035347460354TA49GENIChomozygous139289167
134746039247460393GA39GENIChomozygous139289168
134746052147460522TA48GENICpossibly homozygous139289169
134746087047460871TG65GENICpossibly homozygous139289170
134746093447460935GA63GENIChomozygous139289171
134746107147461072CT37GENIChomozygous139289172
134746132647461326GTGT29GENIChomozygous139171930
134746315447463155CT52GENIChomozygous139289176
134746118847461189TC55GENIChomozygous139289173
134746119447461195AG57GENIChomozygous139289174
134746258247462583GA54GENICpossibly homozygous139289175
134746380047463801TC53GENIChomozygous139289177
134746452847464529GA53GENIChomozygous139289178
134746497247464973GA41GENIChomozygous139289179
134746506247465063TC46GENIChomozygous139289180
134746646547466466TC63GENIChomozygous139289181
134746648547466486T56GENICpossibly homozygous139171931
134746663047466631TC55GENIChomozygous139289182
134746665847466658AAAAA50GENIChomozygous139171932
134746682847466828ATGAGTG24GENIChomozygous139171933
134746685147466852CT31GENIChomozygous139289183
134746687847466879CT36GENIChomozygous139289184
134746690147466902AT38GENIChomozygous139289185
134746699147466992TC45GENIChomozygous139289186
134746704947467050GA52GENIChomozygous139289187
134746734547467346AG44GENIChomozygous139289188
134746771947467720GA60GENIChomozygous139289189
134747183747471838AG58GENIChomozygous139289190
134746689447466894T38GENIChomozygous139171934
134746691247466912G37GENIChomozygous139171935
134746753347467534T43GENIChomozygous139171936
134747240047472404GTGG59GENIChomozygous139171937
134747377247473773TG55GENIChomozygous139289191
134747433647474337CT42GENIChomozygous139289192
134747525447475255AG53GENIChomozygous139289193
134747541747475418CA64GENIChomozygous139289194