chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104589877845898779CCT10GENICpossibly homozygous52052936
104589879245898793TTA10GENICheterozygous51443440
104589879245898793TTAA10GENICpossibly homozygous52193627
104589978545899786CG15GENIChomozygous52193630
104590022745900228CCCCAGGTCCTACACATGCTAGGT30GENIChomozygous52459275
104590082745900828AT22GENIChomozygous52193632