chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143595239143595240TA21GENIChomozygous674165973
4143595754143595755AG28GENIChomozygous674165974
4143596058143596059TA22GENIChomozygous674165975
4143596064143596065TA20GENIChomozygous674165976
4143597231143597232AAATAT28GENIChomozygous770617903
4143598137143598138GGA9GENICheterozygous770617904
4143598137143598138GGAA9GENICheterozygous770617905
4143598221143598222CA19GENIChomozygous674165977
4143599736143599737AG43GENIChomozygous674165978
4143599907143599908TC26GENIChomozygous674165979
4143604440143604441C-22GENIChomozygous770617907
4143604674143604675CT23GENIChomozygous674165980
4143604748143604754ACACCC------20GENIChomozygous770617908
4143605173143605174GA17GENIChomozygous674165981
4143605245143605246AAT25GENIChomozygous770617909
4143605468143605469GT21GENIChomozygous674165982
4143605475143605476TA22GENIChomozygous674165983
4143606027143606028AC27GENIChomozygous674165984
4143606162143606163CT15GENIChomozygous674165985
4143606957143606961TCCC----14GENICpossibly homozygous770617912
4143607052143607053T-22GENIChomozygous770617914
4143607735143607736TG27GENIChomozygous674165986
4143608290143608291GA33GENIChomozygous674165987
4143609090143609091AAAAAG26GENIChomozygous770617915
4143609308143609309AAT15GENICpossibly homozygous770617916
4143609308143609309AATT15GENICheterozygous770617917
4143610209143610210GGTTTT4GENICheterozygous770617921
4143610355143610356AG23GENIChomozygous674165988
4143611152143611153AT19GENIChomozygous674165989
4143611331143611332TTCGGA20GENIChomozygous770617922
4143611504143611505CT25GENICpossibly homozygous674165990
4143611578143611579A-13GENIChomozygous770617923
4143611620143611622AA--17GENICheterozygous770617924
4143611621143611622A-17GENICpossibly homozygous770617925
4143611780143611781TC24GENIChomozygous674165991
4143612095143612096GA9GENIChomozygous674165992
4143612108143612109A-7GENIChomozygous770617926