chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8110306549110306550TC55GENIChomozygous138413615
8110308294110308295TG52GENIChomozygous138413616
8110310886110310887AG50GENIChomozygous138413617
8110311881110311882TC58GENIChomozygous138413618
8110314351110314352AG58GENICpossibly homozygous138413619
8110314798110314799CT46GENIChomozygous138413620
8110318365110318366TC30GENIChomozygous138413621
8110318412110318413CT19GENIChomozygous154544907
8110325496110325497GA55GENIChomozygous138413623
8110325982110325983TC50GENIChomozygous138413624
8110336414110336415TC45GENIChomozygous138413625
8110336522110336523TC47GENIChomozygous138413626
8110342456110342457CT49GENIChomozygous138413627
8110345178110345179CG42GENIChomozygous138413628
8110351774110351774CAT37GENIChomozygous138264400
8110334297110334299GC38GENIChomozygous142030637
8110348970110348971GA73GENIChomozygous138413629
8110350499110350500AG58GENICpossibly homozygous138413630
8110323179110323179GGACCGAACCCAGGGCCTTGC43GENICpossibly homozygous144814421
8110318412110318413C19GENICheterozygous403248998
8110325467110325468GC62GENIChomozygous144829758
8110336196110336197TC29GENICheterozygous144829759
8110336204110336205TC39GENIChomozygous144829760
8110341128110341132AATG31GENIChomozygous138264398
8110345171110345171TAGC42GENIChomozygous138264399
8110336194110336195T29GENICheterozygous146849379
8110336198110336201TTT29GENICheterozygous146849380
8110339672110339673GA6GENICheterozygous147437809
8110351781110351781A37GENIChomozygous138264401
8110351795110351796TC37GENIChomozygous138413633
8110351846110351847T52GENICpossibly homozygous138264402
8110352155110352156AG47GENIChomozygous138413634
8110354057110354058GC44GENIChomozygous138413635
8110354057110354058G44GENICheterozygous403249001
8110357087110357088TG78GENIChomozygous138413636
8110357535110357536TC63GENIChomozygous144829761
8110357831110357832AG57GENIChomozygous138413637
8110358300110358300G57GENIChomozygous138264403
8110360659110360660T55GENIChomozygous138264404