chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101312233913122340TC37GENIChomozygous52029475
101312269313122694CG51GENICheterozygous51328028
101312277213122773TC64GENICheterozygous51328029
101312284113122842GA81GENICheterozygous51328030
101312326513123266AC75GENICheterozygous51328031
101312328713123288AG68GENICheterozygous52029477
101312328813123289CT59GENICheterozygous51328032
101312329813123299GT65GENICheterozygous51620502
101312330613123307TC61GENICheterozygous51328034
101312333213123333TC60GENICheterozygous51328035
101312338513123386AG48GENICheterozygous51620503
101312351913123520AG49GENIChomozygous51328036
101312356013123561GA64GENIChomozygous52029479
101312359913123600TTC67GENIChomozygous51328037
101312373213123733CT81GENICheterozygous52029481
101312374613123747CCAGG33GENICheterozygous51328039
101312375113123757TGTGTC------39GENIChomozygous51328040
101312375313123756TGT---36GENIChomozygous51328041
101312385213123853AT113GENICheterozygous52029483
101312435613124357AG96GENICheterozygous51328042
101312440513124406CA91GENICheterozygous51328043
101312441713124418TG88GENICheterozygous51328044
101312449213124493TC83GENICheterozygous51808527
101312449713124498GGAGA64GENICheterozygous51328045
101312478513124786AG77GENICheterozygous51328046
101312509813125099GT42GENICheterozygous51328049
101312510713125108GT43GENICheterozygous51328050