chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143679952143679953AG20GENIChomozygous115944549
7143680730143680731AG12GENIChomozygous115944550
7143681886143681887AG25GENIChomozygous115944551
7143683081143683082AG15GENIChomozygous115944552
7143684112143684113TA25GENIChomozygous115944553
7143684263143684264C16GENIChomozygous128531469
7143686796143686797AT9GENIChomozygous115944554
7143686884143686884TTTTTCT15GENIChomozygous128531470
7143686959143686960AG18GENIChomozygous115944555
7143687526143687527C19GENIChomozygous128531471
7143687685143687686GC21GENIChomozygous115944556
7143688714143688715TC22GENIChomozygous115944557
7143690747143690747G20GENIChomozygous128531472
7143691009143691010A9GENIChomozygous128531473
7143691650143691651GA20GENIChomozygous115944561
7143689535143689536CT16GENIChomozygous115944558
7143691080143691081AC17GENIChomozygous115944559
7143691435143691436CT28GENIChomozygous115944560
7143693686143693687GC26GENIChomozygous115944562
7143694625143694626AG27GENIChomozygous115944563
7143694943143694944AG23GENIChomozygous115944564
7143695248143695249C28GENIChomozygous128531474
7143695305143695315GGCCTCTATA26GENIChomozygous128531475
7143695427143695428GA18GENIChomozygous115944565
7143696108143696109AG16GENIChomozygous115944566
7143696315143696316TC22GENIChomozygous115944567
7143696579143696580GA21GENIChomozygous115944568
7143696674143696675GC20GENIChomozygous115944569
7143697244143697245GA26GENIChomozygous115944570
7143697671143697672TC24GENIChomozygous115944571
7143700178143700178TT11GENIChomozygous128531476
7143700273143700274TC24GENIChomozygous115944572