chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143595239143595240TA29GENIChomozygous56962816
4143595754143595755AG12GENIChomozygous56962817
4143595803143595804GGCCAA3GENIChomozygous57508157
4143597231143597232AAATAT5GENIChomozygous56962820
4143598137143598138GGA16GENICpossibly homozygous56962822
4143598221143598222CA10GENIChomozygous56962823
4143599736143599737AG22GENIChomozygous57508161
4143599907143599908TC32GENIChomozygous56962825
4143600915143600916A-4GENICheterozygous56962826
4143604440143604441C-19GENIChomozygous56962829
4143604674143604675CT17GENIChomozygous57508163
4143604748143604754ACACCC------20GENIChomozygous57508165
4143605173143605174GA13GENIChomozygous57508167
4143605245143605246AATT9GENICheterozygous56962830
4143605245143605246AAT9GENICpossibly homozygous57508170
4143605468143605469GT16GENIChomozygous56962831
4143605475143605476TA18GENIChomozygous57508172
4143605713143605714TC15GENIChomozygous57508174
4143605997143605998TG17GENIChomozygous57508176
4143606027143606028AC14GENIChomozygous57508178
4143606162143606163CT12GENIChomozygous57508180
4143606292143606293T-12GENICheterozygous57946243
4143606891143606892GGCCTA12GENIChomozygous57508182
4143607052143607053T-25GENIChomozygous56962838
4143607735143607736TG24GENIChomozygous57508184
4143608290143608291GA23GENIChomozygous57508186
4143609090143609091AAAAAG22GENIChomozygous57508188
4143609308143609309AATTT12GENICheterozygous57508190
4143606957143606961TCCC----5GENIChomozygous58343143
4143600914143600916AA--4GENICheterozygous57342418
4143609308143609309AATT12GENICheterozygous57342420
4143610355143610356AG25GENIChomozygous56962841
4143611152143611153AT17GENIChomozygous56962844
4143611621143611622A-19GENICpossibly homozygous57508194
4143611780143611781TC11GENIChomozygous57508196
4143612095143612096GA10GENIChomozygous57508198
4143612108143612109A-12GENICheterozygous56962846
4143612444143612445GA13GENIChomozygous57508200