chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4109473179109473180GT29GENICpossibly homozygous113597901
4109474212109474213GC29GENICpossibly homozygous113372853
4109474449109474450TC31GENICpossibly homozygous113372855
4109474479109474480AG28GENICpossibly homozygous113372857
4109474949109474950CT26GENICpossibly homozygous113372863
4109475070109475071TC26GENIChomozygous113372865
4109475208109475209CT26GENIChomozygous119403564
4109475217109475218CG30GENIChomozygous113372867
4109475522109475523CA26GENICpossibly homozygous113372873
4109475569109475570AG27GENICpossibly homozygous113372875