chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7887107678871077TC8GENIChomozygous108277332
X7887136178871362TC11GENIChomozygous108277334
X7887450978874510CT16GENIChomozygous108277336
X7887548278875483CT13GENIChomozygous108277338
X7887647878876479CT9GENIChomozygous108277340
X7887920078879201CG12GENIChomozygous108277342
X7888043978880440TA11GENIChomozygous108277344
X7888135578881356GA6GENIChomozygous108277346
X7888405678884057GT6GENIChomozygous108277348
X7888937778889378GA15GENIChomozygous108277350
X7889235478892355CT10GENIChomozygous108277352
X7889236778892368TC10GENIChomozygous108277354
X7889467478894675TC12GENIChomozygous108277356
X7889692978896930GT7GENIChomozygous108277358
X7889774178897742AG11GENIChomozygous108620201
X7889810978898110AG18GENIChomozygous108277360
X7890214978902150TC15GENIChomozygous108277362
X7890312978903130TC9GENIChomozygous108277364
X7890440678904407GC11GENIChomozygous108620203
X7890477778904778GA8GENIChomozygous108277366
X7890607178906072AG4GENIChomozygous108277368
X7890752878907529GT11GENIChomozygous108277370
X7890813978908140GA16GENIChomozygous108277372
X7891029678910297AG2GENIChomozygous108632407