chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143595239143595240TA25GENIChomozygous600684617
4143595754143595755AG31GENIChomozygous600684618
4143596309143596310GA26GENIChomozygous603318741
4143597231143597232AAATAT35GENIChomozygous730924009
4143597443143597444AT33GENIChomozygous603318742
4143598137143598138GGA25GENICpossibly homozygous730924010
4143598137143598138GGAA25GENICheterozygous730924011
4143598221143598222CA24GENIChomozygous600684619
4143598596143598597CT40GENIChomozygous603318743
4143599907143599908TC18GENIChomozygous600684620
4143600914143600916AA--15GENICpossibly homozygous730924013
4143600915143600916A-15GENICheterozygous730924014
4143603066143603067A-28GENIChomozygous730924017
4143604389143604390TC25GENIChomozygous603318744
4143604440143604441C-31GENIChomozygous730924018
4143605245143605246AAT20GENICheterozygous730924019
4143605245143605246AATT20GENICpossibly homozygous730924020
4143605468143605469GT26GENIChomozygous600684621
4143606108143606109CCT26GENIChomozygous730924021
4143606224143606225AG34GENIChomozygous603318745
4143606248143606249TC27GENIChomozygous603318746
4143606292143606293T-19GENICheterozygous730924022
4143606935143606936TG28GENIChomozygous603318747
4143606958143606961CCC---18GENIChomozygous730924023
4143607052143607053T-29GENIChomozygous730924025
4143609308143609309AAT27GENICheterozygous730924026
4143609308143609309AATT27GENICheterozygous730924027
4143609647143609650ACG---32GENIChomozygous730924029
4143610209143610210GGT7GENICheterozygous730924031
4143610355143610356AG20GENIChomozygous600684622
4143610545143610546CA19GENIChomozygous603318748
4143610766143610767GA32GENIChomozygous603318749
4143611152143611153AT28GENIChomozygous600684623
4143611578143611579A-28GENIChomozygous730924033
4143612108143612109A-20GENICpossibly homozygous730924034
4143612124143612129AAAAA-----19GENICheterozygous730924036
4143613236143613237AT9GENIChomozygous603318750