chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171503220415032205GC14GENIChomozygous140062438
171503229415032295AT26GENIChomozygous140062439
171503289215032939TCAGAATCTTTGTGCTTGCTTTCGCAACACATACACTAAAATTGGAA18GENIChomozygous140010861
171503301115033012T23GENIChomozygous140010862
171503533215035332A22GENIChomozygous145021640
171503573015035730A23GENIChomozygous140010863
171503356515033567GT22GENIChomozygous143627214
171503583315035833TGACCA18GENIChomozygous143627215
171503451015034511CT22GENIChomozygous143633958
171503473415034735CT21GENIChomozygous143633959
171503541415035415GA30GENIChomozygous143633961
171503433315034334CT20GENIChomozygous146287574
171503653815036539TC21GENIChomozygous143633963
171503660415036605TC20GENIChomozygous143633964
171503754015037541AG21GENIChomozygous143633965
171503779315037794GA22GENIChomozygous143633966
171503980615039807AG18GENIChomozygous143633969
171503991315039914AG21GENIChomozygous140062441
171504278415042785AC18GENIChomozygous143633971
171504280015042801AC16GENIChomozygous143633972
171504326715043268CG18GENIChomozygous140062442
171504438615044387TA10GENIChomozygous143633973
171504579315045794AC20GENIChomozygous140062443
171504660515046606TC22GENIChomozygous143633976
171504670615046707GT18GENIChomozygous143633977
171504716515047166T9GENIChomozygous143627217
171504724015047241TC15GENIChomozygous143633978
171504819015048191CT17GENIChomozygous146287575
171504916615049167TG20GENIChomozygous146287576
171504921715049217G22GENIChomozygous140010864
171504977715049778CT22GENIChomozygous143633980
171505128915051290AG24GENIChomozygous143633981
171505169615051697GA14GENIChomozygous146287577
171505181815051822TGCT15GENIChomozygous140010865
171505077415050775A20GENIChomozygous146284243
171504578015045781A19GENICpossibly homozygous403407774
171504578015045781AC19GENICheterozygous403407773