chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143679952143679953AG40GENIChomozygous115944549
7143680730143680731AG26GENIChomozygous115944550
7143681886143681887AG65GENIChomozygous115944551
7143683081143683082AG53GENIChomozygous115944552
7143684112143684113TA42GENIChomozygous115944553
7143686796143686797AT33GENIChomozygous115944554
7143686959143686960AG37GENIChomozygous115944555
7143687685143687686GC28GENIChomozygous115944556
7143688714143688715TC58GENIChomozygous115944557
7143689535143689536CT44GENIChomozygous115944558
7143691080143691081AC42GENIChomozygous115944559
7143691435143691436CT52GENIChomozygous115944560
7143691650143691651GA49GENIChomozygous115944561
7143693686143693687GC43GENIChomozygous115944562
7143690747143690747G52GENIChomozygous128531472
7143684263143684264C43GENIChomozygous128531469
7143686884143686884TTTTTCT32GENIChomozygous128531470
7143687526143687527C38GENIChomozygous128531471
7143691009143691010A42GENIChomozygous128531473
7143694625143694626AG46GENIChomozygous115944563
7143694943143694944AG41GENIChomozygous115944564
7143695248143695249C44GENIChomozygous128531474
7143695305143695315GGCCTCTATA43GENIChomozygous128531475
7143695427143695428GA47GENIChomozygous115944565
7143696108143696109AG40GENIChomozygous115944566
7143696315143696316TC39GENIChomozygous115944567
7143696579143696580GA45GENICpossibly homozygous115944568
7143696674143696675GC41GENICpossibly homozygous115944569
7143697244143697245GA52GENIChomozygous115944570
7143697671143697672TC42GENIChomozygous115944571
7143700178143700178TT37GENICpossibly homozygous128531476
7143700273143700274TC47GENIChomozygous115944572