chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143679952143679953AG6GENIChomozygous115944549
7143680730143680731AG13GENIChomozygous115944550
7143681886143681887AG23GENIChomozygous115944551
7143683081143683082AG22GENIChomozygous115944552
7143684112143684113TA23GENIChomozygous115944553
7143686796143686797AT9GENIChomozygous115944554
7143687685143687686GC19GENIChomozygous115944556
7143688714143688715TC19GENIChomozygous115944557
7143689535143689536CT25GENIChomozygous115944558
7143691080143691081AC10GENIChomozygous115944559
7143691435143691436CT22GENIChomozygous115944560
7143691650143691651GA9GENIChomozygous115944561
7143693686143693687GC19GENIChomozygous115944562
7143694625143694626AG16GENIChomozygous115944563
7143694943143694944AG28GENIChomozygous115944564
7143695427143695428GA21GENIChomozygous115944565
7143696108143696109AG22GENIChomozygous115944566
7143696315143696316TC22GENIChomozygous115944567
7143696579143696580GA23GENIChomozygous115944568
7143696674143696675GC13GENIChomozygous115944569
7143697244143697245GA17GENIChomozygous115944570
7143697671143697672TC10GENIChomozygous115944571
7143697989143697990AG6GENICheterozygous126541596
7143700177143700178GT4GENICheterozygous126620990
7143700273143700274TC14GENIChomozygous115944572
7143700182143700183GT3GENICheterozygous126588173