chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1203984033203984034GA10GENIChomozygous622830295
1203985006203985007GA9GENIChomozygous622830296
1203985901203985902GA19GENICpossibly homozygous622830297
1203985939203985940AG19GENIChomozygous622830298
1203986413203986414CT11GENIChomozygous622830299
1203986421203986422AT13GENIChomozygous622830300
1203986486203986487AT17GENIChomozygous622830301
1203987362203987363CT17GENICpossibly homozygous622830302
1203987427203987428TTGG3GENICheterozygous740066094
1203988584203988585A-9GENICpossibly homozygous740066095
1203988997203988998TC7GENICheterozygous622830303
1203989090203989091GA8GENICpossibly homozygous622830304
1203989319203989320GT9GENICpossibly homozygous622830305
1203990385203990386AG19GENIChomozygous622830306
1203990500203990501AAT5GENIChomozygous740066096
1203990662203990663TC20GENIChomozygous622830307
1203990852203990853GT15GENICpossibly homozygous622830308
1203990969203990970TG13GENICpossibly homozygous622830309
1203996907203996908AG10GENICpossibly homozygous622830310
1203999511203999512AG2GENIChomozygous622830311
1204000939204000940CT26GENIChomozygous622830312
1204003297204003298TC6GENICheterozygous622830313
1204005989204005990TC8GENICheterozygous622830314
1204006610204006611CG18GENICpossibly homozygous622830315
1204007005204007006AG15GENIChomozygous622830316