chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172776492927764930GT79GENICheterozygous119271561
172776493527764936CT72GENICheterozygous119271562
172776494027764941GA65GENICheterozygous119271563
172776494127764942CT63GENICheterozygous119271564
172776495727764958GA73GENICheterozygous119271565
172776496627764967GA76GENICheterozygous119271566
172776497327764974GA78GENICheterozygous119271567
172776497727764978CT84GENICheterozygous119271568
172776498327764984AC81GENICheterozygous119271569
172776499427764995AG87GENICheterozygous119271570
172776500427765005CA90GENICheterozygous119271571
172776500627765007CT94GENICheterozygous119271572