chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7109574423109574424T22GENIChomozygous145610000
7109614783109614784AG24GENIChomozygous138179490
7109644428109644429AT10GENICheterozygous403222006
7109616663109616664T23GENICpossibly homozygous403221980
7109616663109616664TG23GENICheterozygous403221981
7109644428109644429A10GENICheterozygous403222005
7109644430109644431A12GENICheterozygous403222007
7109644430109644431AT12GENICheterozygous403222008
7109644432109644433A12GENICheterozygous403932712
7109644432109644433AT12GENICheterozygous403932713
7109657500109657501A6GENICheterozygous403222010
7109665961109665962G7GENICheterozygous403222020
7109657500109657501AT6GENICheterozygous403222011
7109657502109657503A6GENICheterozygous404004770
7109657502109657503AT6GENICheterozygous404004771
7109657891109657892GC17GENIChomozygous154492243
7109657891109657892G17GENICheterozygous403222018
7109665961109665962GA7GENICheterozygous403222019
7109668555109668556CT13GENIChomozygous403617230
7109668555109668556C13GENICheterozygous403617231
7109692122109692123GT14GENIChomozygous142007856
7109694870109694871GA25GENIChomozygous146838944
7109692915109692916AG15GENIChomozygous142007857
7109693975109693976GC27GENIChomozygous138179595
7109694233109694234AC25GENIChomozygous146838943
7109694625109694626AG23GENIChomozygous138179596
7109695029109695030AG24GENIChomozygous146838945
7109695061109695062A22GENIChomozygous146820200
7109695784109695785CT30GENIChomozygous146838946
7109696269109696270CT18GENIChomozygous146838947
7109696356109696356AC27GENIChomozygous146820201
7109696456109696457GA43GENIChomozygous146838948
7109696510109696511TA39GENIChomozygous146838949
7109692388109692389GA23GENIChomozygous148021589
7109697412109697413CA20GENIChomozygous148021590
7109698288109698289AG32GENIChomozygous148021591