chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X8404898784048988TC10GENICheterozygous825029240
X8404974784049748CT13GENICheterozygous825029241
X8405074184050742TG9GENICheterozygous825029242
X8405283684052837GT11GENICheterozygous825029243
X8405448784054488AG7GENICheterozygous825029244
X8405519984055200T-14GENIChomozygous825029245
X8405678584056786CG9GENICheterozygous825029246
X8405697484056975TC12GENICheterozygous825029247
X8406163084061631GT9GENICheterozygous825029248
X8406226684062267AG10GENICheterozygous825029249
X8406331884063319CT10GENICheterozygous825029250
X8406813284068133T-10GENICheterozygous825029251
X8406834584068346AG7GENICheterozygous825029252
X8407195284071953TC7GENICheterozygous825029253
X8407267684072677AC6GENIChomozygous825029254
X8407268184072682AT7GENIChomozygous825029255
X8407301084073011G-10GENICheterozygous825029256
X8407798284077983TC7GENICheterozygous825029257
X8407910584079106A-7GENICheterozygous825029258
X8408084484080845GT14GENICheterozygous825029259
X8408146984081470CG17GENICheterozygous825029260
X8408357384083574AT10GENICheterozygous825029261
X8408453884084539GGA17GENICheterozygous825029262
X8408544084085441AATCACCT12GENIChomozygous825029263
X8409072884090729AC6GENICheterozygous825029264
X8409121484091215GA11GENICheterozygous825029265
X8409128084091281CT10GENICheterozygous825029266
X8409130084091301TTAC10GENICheterozygous825029267
X8409570484095705TC8GENICheterozygous825029268
X8410068084100681AT11GENICheterozygous825029269
X8410121984101220GC9GENICheterozygous825029270
X8410349584103496AAT12GENICheterozygous825029271
X8410745884107459AG8GENICheterozygous825029272
X8410748384107484AT7GENICheterozygous825029273
X8411311784113118AT14GENICheterozygous825029274
X8411323484113235GA9GENICheterozygous825029275
X8411451784114527GGTATGTACA----------8GENICheterozygous825029276