chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143595239143595240TA19GENICpossibly homozygous546967685
4143595754143595755AG13GENIChomozygous546967686
4143598221143598222CA14GENIChomozygous546967687
4143599736143599737AG20GENICpossibly homozygous546967688
4143599907143599908TC19GENIChomozygous546967689
4143604440143604441C-5GENIChomozygous698890098
4143604674143604675CT15GENIChomozygous546967690
4143604748143604754ACACCC------13GENICheterozygous698890099
4143605173143605174GA15GENIChomozygous546967691
4143605245143605246AAT5GENIChomozygous698890100
4143605468143605469GT2GENIChomozygous546967692
4143605475143605476TA1GENIChomozygous546967693
4143606027143606028AC4GENIChomozygous546967694
4143606162143606163CT7GENIChomozygous546967695
4143607052143607053T-1GENIChomozygous698890102
4143607735143607736TG21GENIChomozygous546967696
4143608290143608291GA8GENICheterozygous546967697
4143609090143609091AAAAAG7GENIChomozygous698890103
4143610355143610356AG20GENIChomozygous546967698
4143611331143611332TTCGGA10GENIChomozygous698890104
4143611578143611579A-4GENIChomozygous698890105
4143611621143611622A-2GENICheterozygous698890107
4143611780143611781TC19GENIChomozygous546967699