chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1203984033203984034GA5GENIChomozygous645998063
1203984074203984075AG3GENIChomozygous645998064
1203984293203984297TCGG----3GENIChomozygous754698386
1203984737203984738AG13GENIChomozygous645998065
1203985006203985007GA13GENIChomozygous645998066
1203985123203985135GTGTGTGTGTGT------------6GENIChomozygous754698388
1203985901203985902GA20GENIChomozygous645998067
1203985939203985940AG19GENIChomozygous645998068
1203986413203986414CT32GENIChomozygous645998069
1203986421203986422AT31GENIChomozygous645998070
1203986486203986487AT25GENIChomozygous645998071
1203986980203986981CCTCATG11GENIChomozygous754698391
1203986982203986983CCAGGCCTTGTCTTCTTTTTTAA12GENIChomozygous754698392
1203987427203987428TTG9GENIChomozygous754698393
1203988584203988585A-21GENIChomozygous754698395
1203988997203988998TC19GENIChomozygous645998072
1203989090203989091GA32GENIChomozygous645998073
1203989182203989183CCT4GENICheterozygous754698397
1203989182203989183CCTTTTT4GENICheterozygous754698398
1203989319203989320GT19GENIChomozygous645998074
1203990385203990386AG29GENIChomozygous645998075
1203990662203990663TC24GENIChomozygous645998076
1203990852203990853GT27GENIChomozygous645998077
1203990969203990970TG20GENIChomozygous645998078
1203994696203994700ACAC----6GENIChomozygous754698401
1203994719203994720TTAC3GENIChomozygous754698402
1203996907203996908AG23GENIChomozygous645998079
1203997008203997009T-7GENIChomozygous754698403
1203997011203997012GGTGTGT11GENICheterozygous754698405
1203997011203997012GGTGTGTGT11GENICheterozygous754698406
1203999511203999512AG20GENIChomozygous645998080
1203999610203999614TTCA----9GENIChomozygous754698407
1204000096204000097GA6GENIChomozygous645998081
1204000534204000535A-4GENICheterozygous754698408
1204001983204001984AC19GENIChomozygous645998082
1204003297204003298TC22GENIChomozygous645998083
1204006491204006492AG14GENIChomozygous645998084