chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31039896710398968TG71GENICpossibly homozygous143014603
31039996310399964CT53GENIChomozygous143014604
31040059210400593GA60GENIChomozygous136636990
31040069710400698CT53GENIChomozygous143014605
31040560310405603G44GENIChomozygous136548054
31040636210406363CG68GENIChomozygous143014606
31040861810408619TC60GENIChomozygous136636992
31040868510408686GA57GENIChomozygous143014607
31041045310410454TC58GENIChomozygous136636993
31041092110410922TC50GENIChomozygous136636994
31041161810411619GA61GENIChomozygous136636995
31041172210411723TA52GENIChomozygous136636996
31041242010412421GA52GENIChomozygous143014608
31041278710412788TC70GENIChomozygous136636997
31041340510413406GT68GENICpossibly homozygous136636998
31041397610413977AG72GENIChomozygous136636999
31041525210415253TC58GENIChomozygous136637001
31041556010415566GTTTGG48GENICpossibly homozygous136548055
31041577910415780AG64GENIChomozygous136637002
31041611810416119AG54GENICpossibly homozygous143014609
31041786910417870CT47GENICpossibly homozygous143014610
31042031610420317AG57GENIChomozygous136637013
31042513410425135GA56GENIChomozygous143014612
31042605610426057CA46GENIChomozygous143014613
31042616510426166TA49GENIChomozygous136637019
31042707510427076TC56GENIChomozygous136637020
31042763210427633TC28GENIChomozygous136637021
31042766710427669GT28GENICpossibly homozygous136548059
31042790310427904CT47GENIChomozygous143014614
31042951010429511AG60GENIChomozygous136637025
31043430610434307CA66GENIChomozygous143014615
31042168110421682T53GENICheterozygous404061402
31042168110421682TG53GENIChomozygous154087859
31040368910403693AGGG7GENIChomozygous142999360
31042134110421342G35GENICheterozygous404061400
31042134110421342GA35GENICheterozygous404061401