chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7887107678871077TC6GENIChomozygous108277332
X7887136178871362TC10GENIChomozygous108277334
X7887450978874510CT15GENIChomozygous108277336
X7887548278875483CT6GENIChomozygous108277338
X7887647878876479CT10GENIChomozygous108277340
X7887920078879201CG8GENIChomozygous108277342
X7888043978880440TA6GENIChomozygous108277344
X7888135578881356GA4GENIChomozygous108277346
X7888405678884057GT3GENIChomozygous108277348
X7888937778889378GA11GENIChomozygous108277350
X7889235478892355CT16GENIChomozygous108277352
X7889236778892368TC17GENIChomozygous108277354
X7889467478894675TC14GENIChomozygous108277356
X7889692978896930GT3GENIChomozygous108277358
X7889810978898110AG16GENIChomozygous108277360
X7889774178897742AG12GENIChomozygous108620201
X7890041178900412GA43GENICheterozygous120106038
X7890214978902150TC7GENIChomozygous108277362
X7890312978903130TC8GENIChomozygous108277364
X7890440678904407GC7GENIChomozygous108620203
X7890477778904778GA9GENIChomozygous108277366
X7890607178906072AG7GENIChomozygous108277368
X7890752878907529GT5GENIChomozygous108277370
X7890813978908140GA7GENIChomozygous108277372