chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
145945961559459616CG11GENICheterozygous130590331
145945961859459619TA13GENICheterozygous130590332
145945964359459644GT13GENICheterozygous130590333
145946060259460603CT7GENIChomozygous118699431
145946640459466408ATGG14GENIChomozygous129164406
145946697959466979GAAC22GENIChomozygous129164407
145950066359500664G26GENIChomozygous129164418
145950067659500676A23GENIChomozygous129164419
145950069459500695T23GENIChomozygous129164420
145950073759500737G15GENIChomozygous129164421
145950079259500792C12GENIChomozygous129164422
145950085159500852A11GENIChomozygous129164423
145950085559500855C11GENIChomozygous129164424
145950090159500901A18GENIChomozygous129164425
145950091059500911AC18GENIChomozygous113472980
145950099059500990T20GENIChomozygous129164426
145950099959501000G21GENIChomozygous129164427
145950110459501104G14GENIChomozygous129164428
145950170959501709CTA4GENIChomozygous129164429
145950171659501716C4GENIChomozygous129164430
145950173159501731C7GENIChomozygous129164431