chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2180898138180898139AG24GENIChomozygous110800742
2180898172180898173GA22GENIChomozygous110800743
2180899134180899135GA9GENIChomozygous110800745
2180899312180899313AG18GENIChomozygous110800746
2180899631180899632TC24GENIChomozygous110800747
2180899755180899756CT7GENIChomozygous110800748
2180901332180901333TC12GENIChomozygous110800749
2180901794180901795G22GENIChomozygous127711724
2180901789180901791AA21GENIChomozygous127711723
2180899506180899506A15GENIChomozygous127711721
2180901798180901799A20GENIChomozygous127711725
2180901803180901805GG19GENIChomozygous127711726
2180901813180901814C21GENIChomozygous127711727
2180901820180901821G22GENIChomozygous127711728
2180901840180901841G24GENIChomozygous127711729
2180901846180901847C25GENIChomozygous127711730
2180901868180901868T26GENIChomozygous127711731
2180901872180901873A26GENIChomozygous127711732
2180901883180901883GTA23GENIChomozygous127711733
2180901885180901885TT23GENIChomozygous127711734
2180901890180901890T23GENIChomozygous127711735
2180901891180901891AT23GENIChomozygous127711736
2180901886180901887AT23GENIChomozygous127825803
2180902408180902409AG21GENIChomozygous110800750
2180903152180903153AT14GENIChomozygous110800751
2180906629180906630AC20GENIChomozygous110155214
2180907151180907152TC15GENIChomozygous110155215
2180907719180907720TA22GENIChomozygous110800752
2180908056180908057TA16GENIChomozygous110800753
2180908111180908112GA19GENIChomozygous110800754
2180908132180908132T18GENICpossibly homozygous131297243
2180910701180910702AC22GENICpossibly homozygous110155217
2180911479180911480TC33GENIChomozygous110155218
2180911828180911829GA24GENIChomozygous110800756
2180903106180903106TAA18GENIChomozygous131810941
2180903501180903502A21GENIChomozygous131810942
2180906601180906602A19GENIChomozygous131810943