chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2191319151191319152CT33GENIChomozygous136418118
2191319784191319785TA63GENIChomozygous136418119
2191320797191320798CT33GENIChomozygous136418120
2191322261191322262GA58GENIChomozygous136418121
2191322665191322666CT54GENIChomozygous136418122
2191325546191325547GA72GENIChomozygous136418123
2191325777191325778CT55GENIChomozygous136418124
2191325939191325941TG64GENIChomozygous135968857
2191322348191322348T56GENICpossibly homozygous135968854
2191325803191325831TGCATCACCAGTGCTCGTATTTAAAGTG49GENIChomozygous135968855
2191325936191325936TT62GENIChomozygous135968856
2191325939191325940TC64GENICheterozygous403034032
2191325936191325937CA63GENIChomozygous403034029
2191325936191325937CT63GENICheterozygous403034030
2191325939191325940T64GENIChomozygous403034031
2191325949191325950GA66GENIChomozygous136418125
2191325996191325997TA63GENIChomozygous136418126
2191325997191325998CT63GENIChomozygous136418127
2191326907191326908GT47GENIChomozygous136418128
2191327061191327062GA58GENIChomozygous136418129
2191328712191328713TC43GENIChomozygous136418130
2191329707191329708AG55GENIChomozygous136418131