chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153770935937709359T18GENICheterozygous131935314
153774590737745907T12GENIChomozygous129246377
153778163937781639G19GENIChomozygous130149008
153778168137781682T25GENIChomozygous130149009
153778169637781699CTA23GENIChomozygous130149010
153778172637781729CAA17GENIChomozygous130149011
153778173537781736T16GENIChomozygous130149012
153778174837781749C16GENIChomozygous130149013
153778175137781752T16GENIChomozygous130149014
153778176337781764A16GENIChomozygous130440407
153778176637781767A13GENICheterozygous130592484
153778179837781847ACACACAACCCATATACACATATAAAACACAACAATACAACAACACACC8GENIChomozygous130698572
153778205937782060T10GENIChomozygous130592485
153778208037782081C12GENIChomozygous130592486