chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214399741439975AG8GENICpossibly homozygous50001069
1214413861441387CT5GENIChomozygous50393748
1214451501445151AC17GENIChomozygous50001074
1214452701445271AT28GENIChomozygous50001075
1214456221445623AG17GENICpossibly homozygous50001076
1214470971447098CT22GENICpossibly homozygous50001077
1214473901447392GT--3GENIChomozygous50503138
1214474181447422GTGT----10GENIChomozygous50001082
1214479231447924CT7GENICpossibly homozygous50393750
1214487651448766CCGTGTCTGT1GENIChomozygous50393752
1214495571449558TA19GENICpossibly homozygous50393754
1214495651449566CCGT5GENICheterozygous50503139