chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77069371970693720AG26GENICpossibly homozygous53957188
77069399370693994AG5GENICheterozygous53957190
77069407070694071CG8GENICheterozygous53957191
77069567070695671AG23GENICpossibly homozygous53957193
77069720770697208GA13GENICpossibly homozygous53957194
77069726770697268TC24GENIChomozygous53957196
77069924770699248CT25GENICpossibly homozygous53957199
77070747270707473AG26GENIChomozygous53957207
77071026470710265TC22GENICpossibly homozygous53957212
77071056570710566AC20GENIChomozygous53957214
77071108170711082CCA15GENIChomozygous53957216
77071154170711542AG18GENICpossibly homozygous53957218
77071334070713341TTA11GENICpossibly homozygous53957220
77071419970714200CT14GENICpossibly homozygous53957222
77071635070716351AT18GENICpossibly homozygous53957230
77071659370716594TA13GENICpossibly homozygous53957233
77071709670717097GA12GENIChomozygous53957237
77071753470717535TC19GENIChomozygous53957239
77071983070719831G-13GENIChomozygous53957241
77072492670724927TC21GENICpossibly homozygous53957247
77072508970725090TG17GENICpossibly homozygous53957249