chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3124842311124842312AG20GENICpossibly homozygous57651830
3124843095124843096CT18GENICpossibly homozygous57651831
3124844927124844928AG16GENICpossibly homozygous57651833
3124846563124846564AAT1GENIChomozygous57651835
3124846681124846682CT20GENICpossibly homozygous57651837
3124846813124846814CT17GENICpossibly homozygous57651839
3124847356124847357GA22GENICpossibly homozygous57651841
3124848843124848844AG15GENICheterozygous57651843
3124849612124849613AC3GENIChomozygous57651847
3124849879124849880GA13GENICpossibly homozygous57651849
3124851406124851407CT17GENIChomozygous57651853
3124853322124853323CA4GENIChomozygous57651857
3124855762124855763GA10GENICheterozygous57651863
3124855777124855778AG10GENIChomozygous57651865
3124857418124857419AT10GENICpossibly homozygous57651867
3124859394124859396CC--6GENIChomozygous57651869
3124859399124859400CG6GENIChomozygous58651747
3124860039124860040A-4GENIChomozygous57651871
3124860413124860414GA24GENIChomozygous57651873
3124860843124860844CT8GENIChomozygous57651875
3124861483124861484CA13GENICheterozygous57651877
3124863084124863085AG20GENICpossibly homozygous57651879
3124864243124864244TC21GENIChomozygous57651881
3124865002124865003CT14GENIChomozygous57651883
3124865065124865066AAAATAT5GENIChomozygous57651885
3124866031124866032AG23GENIChomozygous57651887
3124866344124866345AAGG1GENIChomozygous58694623
3124876306124876316AAAGCAAAGC----------5GENIChomozygous57651893
3124877982124877983AC4GENICheterozygous57651897
3124878193124878194GA15GENIChomozygous57651899
3124879719124879720AG23GENICpossibly homozygous57651901
3124880299124880300CA12GENIChomozygous57651903
3124881087124881088CT14GENIChomozygous57651905
3124883429124883430CT5GENIChomozygous57651907
3124883448124883449GT2GENIChomozygous57651909
3124883533124883534CT18GENICpossibly homozygous57651911
3124884616124884617CT20GENIChomozygous57651913
3124885192124885193T-2GENICheterozygous57651915
3124892499124892500GA7GENIChomozygous57651921