chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170239257170239258TG12GENIChomozygous108375341
1170239558170239559TA24GENIChomozygous108375343
1170239646170239647CT26GENIChomozygous108375345
1170239746170239747TC26GENIChomozygous108375347
1170240018170240019AG28GENIChomozygous108375349
1170240072170240073AG22GENIChomozygous108375351
1170240142170240143TC37GENIChomozygous108375353
1170240229170240230AG27GENIChomozygous108375355
1170240493170240494TC27GENIChomozygous108375357
1170240851170240852CT27GENIChomozygous108375359
1170241108170241109TC27GENIChomozygous108375361
1170241153170241154AG33GENIChomozygous108375363
1170241325170241326CT28GENIChomozygous108375365
1170241380170241381AG24GENIChomozygous108375367
1170241608170241609CT34GENIChomozygous108375369
1170241983170241984GA26GENIChomozygous108375373
1170242169170242170TC31GENIChomozygous108375375
1170242437170242438GA30GENIChomozygous108375377
1170242844170242845CA17GENIChomozygous108375379
1170243342170243343GA20GENIChomozygous108375381
1170243410170243411CT29GENIChomozygous108375383
1170243568170243569TA18GENIChomozygous108375385
1170243701170243702CT13GENIChomozygous108375387
1170243732170243733AG14GENIChomozygous108375389
1170244720170244721AG22GENIChomozygous108375395
1170245331170245332AG21GENIChomozygous108375397
1170246029170246030TC28GENIChomozygous108375399
1170246206170246207CG23GENIChomozygous108375401
1170246435170246436TC23GENIChomozygous108375407
1170246827170246828CA21GENIChomozygous108375411