chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141084689141084690T-12GENIChomozygous689104904
5141084698141084699TG15GENIChomozygous517652668
5141084883141084884TC28GENIChomozygous517652669
5141085723141085724GA40GENIChomozygous515637681
5141086046141086047A-16GENICheterozygous689104905
5141096883141096884GGCA22GENICheterozygous689104907
5141096884141096886CA--22GENICheterozygous689104906
5141096907141096923ACATGCACACACACGT----------------17GENIChomozygous689104908
5141096921141096923GT--22GENICpossibly homozygous689104909
5141096958141096960CA--25GENIChomozygous689104910
5141097370141097371AC33GENIChomozygous517652670
5141097379141097380GA32GENIChomozygous517652671
5141099137141099138G-35GENICheterozygous689104911
5141099152141099153GA28GENICheterozygous517652672
5141099157141099158GA27GENICheterozygous517652673
5141099337141099338TA16GENIChomozygous515637682
5141099588141099589GA28GENIChomozygous517652674
5141099912141099913AG26GENIChomozygous515637683
5141100283141100284G-38GENIChomozygous689104912
5141100455141100456CT32GENIChomozygous517652675
5141101227141101228TC35GENIChomozygous515637684
5141102733141102736AAA---20GENICheterozygous689104914
5141102741141102742AAAAAAGAAAAAAG26GENIChomozygous689104915
5141103569141103570AG30GENICpossibly homozygous515637685
5141103971141103972GA38GENIChomozygous515637686
5141104990141105002TGTGTGTGTGTG------------6GENICheterozygous689104916
5141105021141105022GC18GENICpossibly homozygous515637687
5141106819141106820TC30GENIChomozygous515637688
5141108057141108058A-4GENIChomozygous689104918
5141108237141108238CT24GENIChomozygous517652676
5141109664141109665CT18GENIChomozygous517652677
5141109884141109885GA22GENIChomozygous517652678
5141110764141110765T-1GENIChomozygous689104920