chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14112892818112892819CT10GENICpossibly homozygous546187207
14112893528112893530TT--8GENICheterozygous698536770
14112893616112893617GA19GENIChomozygous547951934
14112893830112893831GA4GENICheterozygous546187208
14112894401112894402AG16GENICpossibly homozygous546187209
14112894677112894678GA13GENIChomozygous547951935
14112896800112896801TC19GENIChomozygous546187210
14112897304112897305TG25GENIChomozygous546187211
14112897844112897845CT14GENICpossibly homozygous547951936
14112897945112897946AG24GENIChomozygous546187212
14112898410112898411AG7GENIChomozygous546187213
14112898466112898467AG22GENIChomozygous546187214
14112900406112900407AG13GENIChomozygous547951937
14112901291112901292CT29GENICpossibly homozygous547951938
14112901734112901735GA18GENICpossibly homozygous547951939