chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185122578851225789AG15GENIChomozygous528552087
185122609651226097TC23GENIChomozygous528552088
185122791151227912GT9GENIChomozygous528552089
185122798951227990CCTTG10GENIChomozygous694862295
185122830651228307TC12GENIChomozygous531826849
185122983651229837TC16GENIChomozygous531826850
185122987351229874CCTTTATTTATTTA7GENIChomozygous694862296
185122998551229986TC17GENIChomozygous531826851
185123018151230182GA14GENIChomozygous528552090
185123098851230989CT6GENIChomozygous531826852
185123333751233338GC14GENIChomozygous528552091
185123459951234600GA15GENIChomozygous528552092
185123504451235045AG19GENIChomozygous528552093
185123516351235164TC16GENIChomozygous531826853
185123666751236668CA19GENIChomozygous528552094
185123776851237769TA19GENIChomozygous531826854
185123784151237842TTATTC12GENIChomozygous694862297
185123840051238401TC19GENICpossibly homozygous528552095
185123980051239801GGA16GENIChomozygous694862298
185124015051240152TT--10GENICheterozygous694862299
185124015151240152T-10GENICheterozygous694862300
185124096151240962AG14GENIChomozygous528552096
185124190851241909AG16GENICpossibly homozygous528552097
185124202551242026GA22GENIChomozygous528552098
185124220951242210AG13GENIChomozygous528552099
185124238851242389CT19GENIChomozygous528552100
185124260851242609AC22GENIChomozygous528552101
185124313551243136TC18GENIChomozygous528552102
185124338951243390GT32GENIChomozygous531826855