chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143595239143595240TA10GENIChomozygous56962816
4143595754143595755AG33GENIChomozygous56962817
4143595803143595804GGCCAA25GENIChomozygous57508157
4143597231143597232AAATAT3GENIChomozygous56962820
4143598137143598138GGA21GENICpossibly homozygous56962822
4143598137143598138GGAA21GENICheterozygous57508159
4143598221143598222CA23GENIChomozygous56962823
4143599736143599737AG31GENIChomozygous57508161
4143599907143599908TC38GENIChomozygous56962825
4143600915143600916A-2GENIChomozygous56962826
4143604440143604441C-12GENIChomozygous56962829
4143604674143604675CT22GENIChomozygous57508163
4143604748143604754ACACCC------17GENIChomozygous57508165
4143605173143605174GA16GENIChomozygous57508167
4143605245143605246AAT4GENIChomozygous57508170
4143605468143605469GT4GENIChomozygous56962831
4143605475143605476TA5GENIChomozygous57508172
4143605713143605714TC13GENIChomozygous57508174
4143605997143605998TG8GENIChomozygous57508176
4143606027143606028AC12GENIChomozygous57508178
4143606162143606163CT7GENIChomozygous57508180
4143606292143606293T-11GENICheterozygous57946243
4143606891143606892GGCCTA19GENIChomozygous57508182
4143606957143606961TCCC----8GENIChomozygous58343143
4143607052143607053T-2GENIChomozygous56962838
4143607735143607736TG22GENIChomozygous57508184
4143608290143608291GA28GENIChomozygous57508186
4143609090143609091AAAAAG36GENIChomozygous57508188
4143609308143609309AATTT5GENIChomozygous57508190
4143610209143610210GGT8GENICheterozygous58567672
4143610355143610356AG22GENIChomozygous56962841
4143611152143611153AT11GENIChomozygous56962844
4143611621143611622A-20GENIChomozygous57508194
4143611780143611781TC18GENIChomozygous57508196
4143612095143612096GA6GENIChomozygous57508198
4143612108143612109A-6GENIChomozygous56962846
4143612444143612445GA15GENIChomozygous57508200