chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1203742700203742701TC18GENIChomozygous144572310
1203745673203745674GA16GENIChomozygous144260871
1203750139203750140GT12GENIChomozygous144260872
1203750686203750687AG24GENIChomozygous135791422
1203750822203750823GA18GENIChomozygous144572311
1203751032203751033GC16GENIChomozygous144572312
1203752403203752404AT11GENICpossibly homozygous144572313
1203752720203752721CT20GENIChomozygous144572314
1203752763203752764T6GENIChomozygous402979306
1203752763203752764TG6GENICheterozygous402979307
1203752765203752766T6GENIChomozygous402979308
1203752765203752766TG6GENICheterozygous402979309
1203752767203752768TG6GENICheterozygous402979310
1203752767203752768T6GENIChomozygous402979311
1203752769203752770TG6GENICheterozygous402979312
1203752769203752770T6GENIChomozygous402979313
1203755989203755990TC18GENICheterozygous153909208
1203755989203755990T18GENICheterozygous402979317
1203757413203757414GC13GENIChomozygous135791425
1203758346203758347GT24GENIChomozygous144572315
1203758641203758642GT18GENIChomozygous144260875
1203759612203759613AG22GENIChomozygous135791426
1203759951203759952GA18GENIChomozygous144572316
1203761144203761145TC18GENIChomozygous144572317
1203762562203762563TC20GENIChomozygous135791427
1203762590203762591GA17GENIChomozygous144572318
1203763168203763169CT23GENIChomozygous144260882
1203763758203763759AC19GENIChomozygous135791428
1203756023203756023TG21GENIChomozygous144231302
1203771110203771110A17GENIChomozygous140959067
1203756375203756375A13GENIChomozygous144529561
1203760930203760930C2GENIChomozygous144529562
1203767036203767036TCTA9GENIChomozygous144529563