chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X122657990122657991TG8GENICheterozygous45212662
X122658616122658617AG60GENICheterozygous45212671
X122658661122658662CA62GENICheterozygous45212672
X122658699122658700GT56GENICheterozygous45212673
X122658721122658722GA45GENICheterozygous45212674
X122658733122658734CT47GENICheterozygous45212675
X122658895122658896T-34GENICheterozygous45212676
X122696855122696856C-11GENICheterozygous45212721
X122696946122696947TA22GENICheterozygous45212722
X122729358122729359AG11GENICheterozygous45212806
X122732187122732188GA21GENICheterozygous45212819
X122734488122734489AC19GENICheterozygous45212829
X122737693122737694AG10GENICheterozygous45212836
X122742234122742235AG15GENICheterozygous45212843
X122751423122751424TC19GENICheterozygous45212861
X122758486122758487GGA18GENICheterozygous45212874
X122826243122826244AG30GENICheterozygous45212888