chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2239134871239134872GT7GENIChomozygous110631830
2239135104239135105GT22GENIChomozygous110329261
2239136045239136046AC12GENICheterozygous110329263
2239136281239136282CG6GENIChomozygous125631158
2239136349239136350AG7GENIChomozygous125631159
2239136463239136464GC24GENIChomozygous125609634
2239137737239137738CT15GENIChomozygous125609635
2239138434239138435TG17GENICheterozygous125673729
2239141459239141460GA9GENIChomozygous110841615
2239142953239142954CG16GENIChomozygous110329267
2239143042239143043CT19GENIChomozygous110841616
2239144081239144082AG7GENIChomozygous110329271
2239145370239145371CT18GENIChomozygous110329273
2239145888239145889AT17GENIChomozygous110841617
2239146152239146153TC19GENIChomozygous110329277
2239149933239149934GT22GENIChomozygous110329309
2239150161239150162TC6GENIChomozygous110841627
2239155085239155086CT20GENIChomozygous110329313
2239157704239157705GA24GENIChomozygous110329323
2239158071239158072CA21GENIChomozygous110329325
2239159328239159329TG14GENIChomozygous110329334
2239160335239160336TC13GENIChomozygous110329340
2239160397239160398TC10GENIChomozygous110329342
2239160844239160845CG15GENIChomozygous110329344
2239162313239162314GA14GENIChomozygous110841628
2239162439239162440TC11GENIChomozygous110841629
2239162877239162878CT17GENIChomozygous110841630
2239163119239163120AC7GENIChomozygous110841631
2239163162239163163CT11GENIChomozygous110841632
2239164618239164619GA14GENIChomozygous110329366
2239165087239165088TC23GENIChomozygous110329368
2239165351239165352CT10GENIChomozygous110329370
2239165419239165420GA10GENIChomozygous110329372