chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225953768225953769CCT2GENICheterozygous61103399
1225955993225955994GGGT1GENIChomozygous62546842
1225956100225956101TC3GENIChomozygous61321617
1225956101225956102CT3GENIChomozygous62102893
1225956387225956388A-4GENIChomozygous61103409
1225956399225956400A-4GENIChomozygous61103410
1225956402225956403AT4GENIChomozygous61103411
1225956409225956410TC4GENIChomozygous61601601
1225956410225956411AT4GENIChomozygous61601603
1225960659225960660GGCTTTAGA8GENIChomozygous61103426
1225960699225960700GGT6GENIChomozygous61103427
1225961785225961786A-5GENICheterozygous61321618
1225973178225973179C-3GENICheterozygous62201608
1225973640225973641A-5GENICheterozygous61321619
1225974352225974353CCAT5GENIChomozygous61103471
1225974353225974354GGT5GENIChomozygous61103472
1225984587225984588CA2GENIChomozygous61103488
1225989023225989024TTAGAA7GENIChomozygous62201610
1225989751225989752CCA5GENICheterozygous61103500
1225993946225993947T-7GENICheterozygous62355257