chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1288092118809212TC20GENIChomozygous50036222
1288092228809223GGGCCTCATCCCGGCA23GENIChomozygous50036226
1288092678809268AG29GENIChomozygous50036228
1288134358813436A-7GENICpossibly homozygous50036230
1288134548813455TA8GENIChomozygous50036232
1288158698815870TC13GENIChomozygous50036237
1288159328815933GA19GENIChomozygous50036239
1288159688815969CG19GENIChomozygous50036241
1288160438816044TC24GENIChomozygous50036243
1288160538816054AG24GENIChomozygous50036245
1288161028816103GA25GENIChomozygous50036247
1288161808816181CCACTT24GENIChomozygous50036249
1288163328816333AG22GENIChomozygous50036251
1288163628816363CT26GENIChomozygous50036253
1288164108816413CTT---23GENIChomozygous50036257
1288164358816436CT23GENIChomozygous50036261
1288180388818042ACAC----6GENICheterozygous50529127
1288174498817451TG--2GENICheterozygous50529121
1288179648817965CCCTCTCT3GENIChomozygous50529123
1288180368818042ACACAC------6GENICheterozygous50529125
1288183438818344AAT12GENICpossibly homozygous50036267
1288187178818718GGTGTCTCTC21GENIChomozygous50036270
1288188028818804TC--16GENIChomozygous50036274
1288192178819218AAAG4GENICheterozygous50529129
1288213408821341CG11GENIChomozygous50036276
1288214998821500CCTCCTCTCCTCTCCTCTCCTCTCCT2GENIChomozygous50529131
1288257868825788AT--1GENIChomozygous50036278