chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95202480552024806CT19GENIChomozygous117337979
95202524352025244AG8GENIChomozygous117337981
95202689752026898AC15GENIChomozygous117337982
95202764352027644TC23GENIChomozygous117337983
95202771052027711GC25GENIChomozygous117337984
95202832952028330GA18GENIChomozygous117337985
95202854952028550CG13GENIChomozygous117337986
95203071352030714CT10GENIChomozygous117337987
95203115852031159TC16GENIChomozygous117337988
95203286652032867GA19GENIChomozygous117337989
95203587252035873CT10GENIChomozygous117337990
95203684052036841CT18GENIChomozygous117337991
95203725452037255GA7GENIChomozygous117337992
95203840552038406AG17GENIChomozygous117337993
95203990552039906CT22GENIChomozygous117337994
95204119752041198TC8GENIChomozygous117337995
95204496952044970CG36GENICheterozygous117797917
95204537152045372TC16GENIChomozygous117337996
95204557752045578CA24GENIChomozygous117337997
95204666752046668AT13GENIChomozygous117337998
95204739652047397TC10GENIChomozygous117337999
95204750952047510TA19GENIChomozygous117338000
95204980652049807TC42GENICheterozygous117338001
95205003952050040TG24GENIChomozygous117338002
95205161752051618AG14GENIChomozygous117338003
95205207252052073GT15GENIChomozygous117338004
95205219452052195TC19GENIChomozygous117338005
95205248552052486CT13GENIChomozygous117338006
95205255052052551GA20GENIChomozygous117338007
95205308952053090TA7GENIChomozygous117338008
95205554152055542AG7GENIChomozygous117338009
95205611652056117CT18GENIChomozygous117338010
95205653052056531GA11GENIChomozygous117338011
95205682552056826TG7GENIChomozygous117338012
95205702952057030GA13GENIChomozygous117338013
95205751952057520CT4GENIChomozygous117338014
95205793752057938CT23GENIChomozygous117338015
95205834652058347TC12GENIChomozygous117338016
95205842052058421CT13GENIChomozygous117338017
95205860052058601GA16GENIChomozygous117338018