chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185122578851225789AG29GENIChomozygous552336290
185122609651226097TC33GENIChomozygous552336291
185122791151227912GT25GENIChomozygous552336292
185122798951227990CCTTG26GENIChomozygous702184763
185122830651228307TC31GENIChomozygous555126665
185122983651229837TC17GENIChomozygous555126666
185122987351229874CCTTTATTTATTTA4GENICheterozygous702184765
185122987351229874CCTTTATTTATTTATTTA4GENICheterozygous702184766
185122998551229986TC9GENIChomozygous555126667
185123018151230182GA16GENIChomozygous552336293
185123067951230685GAGAGA------8GENICheterozygous702184767
185123098851230989CT26GENIChomozygous555126668
185123333751233338GC17GENIChomozygous552336294
185123368851233689A-21GENIChomozygous702184768
185123459951234600GA27GENIChomozygous552336295
185123504451235045AG45GENIChomozygous552336296
185123516351235164TC28GENIChomozygous555126669
185123666751236668CA17GENIChomozygous552336297
185123784151237842TTATTC8GENIChomozygous702184769
185123840051238401TC37GENIChomozygous552336298
185123980051239801GGA16GENIChomozygous702184770
185123999951240017TGTGTGTGTGTGTGTGTG------------------12GENICheterozygous702184773
185124000151240017TGTGTGTGTGTGTGTG----------------12GENICheterozygous702184774
185124015051240152TT--14GENIChomozygous702184776
185124096151240962AG36GENIChomozygous552336299
185124190851241909AG21GENIChomozygous552336300
185124202551242026GA26GENIChomozygous552336301
185124220951242210AG28GENIChomozygous552336302
185124238851242389CT40GENIChomozygous552336303
185124260851242609AC31GENIChomozygous552336304
185124313551243136TC21GENIChomozygous552336305
185124338951243390GT5GENIChomozygous555126670