chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113180750931807510TG20GENIChomozygous115812546
113180983031809831AC15GENIChomozygous115812548
113181084831810849GA14GENIChomozygous115812550
113181132331811324TG11GENIChomozygous115812552
113181208631812087TG13GENIChomozygous115812554
113181660731816608CT6GENIChomozygous115812558
113181663031816631TC14GENIChomozygous115812560
113181727131817272GA17GENIChomozygous115812562
113181950631819507CT7GENIChomozygous115812564
113181971831819719CA29GENIChomozygous115812566
113181985231819853CG16GENIChomozygous115812568
113182459931824600AC10GENIChomozygous115812570
113182610731826108TC17GENIChomozygous115812572
113182619331826194TC13GENIChomozygous115812574
113182708631827087TC9GENIChomozygous115812578
113182824231828243GA10GENIChomozygous115812580
113182866931828670CG6GENIChomozygous115812582
113182954131829542GA11GENIChomozygous115812584
113183360331833604TC12GENIChomozygous115812586
113183487131834872TC12GENIChomozygous115812588
113183570931835710TC14GENIChomozygous115812590
113183629031836291CT14GENIChomozygous115812592
113183644131836442GA17GENIChomozygous115812594
113183647831836479AT16GENIChomozygous115812596