chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1180226727180226729TG--7GENICpossibly homozygous60982294
1180227097180227098GGTT13GENICpossibly homozygous60982296
1180227097180227098GGTTT13GENICheterozygous61312943
1180227308180227309GT22GENIChomozygous60982298
1180229583180229584CT14GENIChomozygous60982300
1180229666180229667TG20GENIChomozygous60982302
1180231222180231223CT38GENIChomozygous60982304
1180231537180231538CCT21GENIChomozygous60982306
1180231906180231907TTGAGAGAGA7GENICheterozygous60982308
1180231942180231943AAGAGAGAGAGAGAGAGAG25GENICheterozygous62313676
1180232457180232458CCAAGAAAGAAAGAAAGAAAGAAAGAAAGA1GENIChomozygous62517729
1180233584180233585AC26GENIChomozygous60982314
1180233636180233637AG18GENIChomozygous60982316
1180234050180234051TC29GENIChomozygous60982318
1180234392180234393AG44GENIChomozygous60982320
1180235882180235883AAG22GENICheterozygous62313677
1180235914180235915T-20GENICheterozygous62234402
1180236227180236228AAG3GENIChomozygous60982336
1180237009180237010CG25GENIChomozygous60982338
1180241766180241767TC39GENIChomozygous60982342
1180242189180242190GA31GENIChomozygous60982344
1180242263180242264CCCTGGGCTCTTTTTGG3GENICheterozygous62179545
1180244184180244186AA--19GENIChomozygous60982346
1180244189180244191CA--21GENIChomozygous60982348
1180244452180244453GGAAGGAGGCACGATCTCC2GENIChomozygous60982350
1180246087180246088AG28GENIChomozygous60982358
1180246171180246172TC24GENIChomozygous60982360
1180250278180250279GA28GENIChomozygous60982362
1180250957180250958CA46GENIChomozygous60982364
1180251600180251601CT28GENIChomozygous60982366