chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101891372718913847TTAAAGCAAAATCGCAGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGGAAAAAAAGAACAAAAAAAAAAAAAAAGAG------------------------------------------------------------------------------------------------------------------------21GENICheterozygous52313871
101891435018914351TA15GENIChomozygous51630224
101891456618914567GGT1GENIChomozygous51337788
101891467418914675GA18GENICpossibly homozygous51630225
101891488318914884AG19GENIChomozygous51337789
101891514518915146AAAG14GENIChomozygous51337795
101891599818915999TC23GENIChomozygous51337802
101891634818916349CT23GENICpossibly homozygous51630227
101891704418917045GA12GENICpossibly homozygous51630228
101891893118918932AG20GENICpossibly homozygous51337821
101891903118919032GT4GENIChomozygous51630229
101891904218919043AG14GENICpossibly homozygous51630230
101892025318920254GA29GENICpossibly homozygous51630231
101892058618920587CT15GENICpossibly homozygous51630232
101892107118921072CT21GENICpossibly homozygous51337831
101892157118921572TC19GENICpossibly homozygous51337837
101892275218922753GA28INTERGENIChomozygous51630235