chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137403536574035366TC21GENIChomozygous114391218
137403735074037351GA33GENIChomozygous114391222
137403758074037581GA29GENIChomozygous114896148
137403936774039368GA24GENIChomozygous114391224
137404009274040093GA21GENIChomozygous114896150
137404020074040201CA26GENIChomozygous114896152
137404598774045988AG30GENIChomozygous114391228
137404847674048477CA15GENIChomozygous114391230
137404874274048743CA19GENIChomozygous114391232
137404907274049073TC17GENIChomozygous114391234
137405019974050200GA25GENIChomozygous114391236
137405082574050826GA6GENIChomozygous114391238
137405308774053088CT33GENIChomozygous114896154
137405541574055416TC33GENIChomozygous114896156
137405709974057100TC31GENIChomozygous114391244
137405736974057370CT22GENIChomozygous114391246
137405900074059001AT15GENIChomozygous114896158
137406095174060952GA27GENIChomozygous114391248
137406255174062552GT31GENIChomozygous114391250
137406372874063729GA16GENIChomozygous114391254
137406415374064154GA22GENIChomozygous114896160
137406523874065239TC34GENIChomozygous114391256
137406564674065647AG22GENIChomozygous114640196
137406690974066910CT14GENIChomozygous114896162
137406711174067112AC12GENIChomozygous114896164
137406722774067228AG16GENIChomozygous114896166
137406756874067569AG19GENIChomozygous114640202
137407080274070803TC20GENIChomozygous114896168
137407124474071245AT30GENICpossibly homozygous114391260
137407204074072041GA7GENIChomozygous114896170
137407206874072069AC5GENICheterozygous114896172
137407207074072071AC4GENICheterozygous114896174
137407367274073673AT16GENIChomozygous114896176
137407413874074139CT27GENIChomozygous114896178
137407500874075009AG16GENIChomozygous114640235
137407656874076569TC7GENIChomozygous114724322
137407660774076608CG3GENIChomozygous114391268
137407660974076610TC3GENIChomozygous114391270
137407732674077327CT23GENIChomozygous114896180