chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101312188613121887GA13GENIChomozygous51620488
101312198013121981GT9GENIChomozygous51620489
101312201213122013GA5GENIChomozygous51620490
101312202913122030CCGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCT2GENIChomozygous53329167
101312208213122083CCTGTGTGTGT5GENIChomozygous53329170
101312208313122084AT5GENIChomozygous53329172
101312208913122097AGTTCTCA--------6GENIChomozygous53329174
101312270613122722AGGGACGCAGCTGGAG----------------29GENICheterozygous52356224
101312278413122785GA23GENIChomozygous51620495
101312281613122817G-36GENICheterozygous51620496
101312310113123102G-28GENICheterozygous51620500
101312326513123266AC37GENIChomozygous51328031
101312330613123307TC30GENIChomozygous51328034
101312338513123386AG23GENIChomozygous51620503
101312351913123520AG18GENIChomozygous51328036
101312359913123600TTC29GENIChomozygous51328037
101312435613124357AG48GENICheterozygous51328042
101312441113124412AG38GENIChomozygous51620509
101312441713124418TG41GENICheterozygous51328044
101312449713124498GGAGA36GENICheterozygous51328045
101312527313125274CT9GENIChomozygous51620514