chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15102579008102579009CA42GENIChomozygous112827044
15102579115102579116GA29GENIChomozygous112763388
15102579171102579172CT30GENIChomozygous112763390
15102579817102579818TC25GENIChomozygous112626504
15102580139102580140GA18GENIChomozygous112626506
15102580164102580165GT23GENIChomozygous112626508
15102580207102580208AG21GENIChomozygous112626511
15102580217102580218CT17GENIChomozygous112626513
15102580578102580579TC16GENIChomozygous112626515
15102580628102580629TC23GENIChomozygous112626517
15102581090102581091CT14GENIChomozygous112827046
15102582928102582929TC20GENIChomozygous112626519
15102583926102583927CA14GENIChomozygous112626521
15102584923102584924TA24GENIChomozygous112626523
15102585612102585613AG14GENIChomozygous112626525
15102586678102586679CT22GENIChomozygous112626527
15102586827102586828TA10GENIChomozygous112626529
15102586856102586857CT10GENIChomozygous112626532
15102587518102587519TC28GENIChomozygous112626534