chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
792811739281174G26GENIChomozygous146435033
792815659281566TC17GENIChomozygous137999903
792828279282828GT6GENIChomozygous154428467
792828279282828G6GENICheterozygous403199547
792843829284383GC35GENIChomozygous146446231
792850689285068C29GENICpossibly homozygous146435034
792851579285158TC14GENIChomozygous137999905
792865159286639CTGTACTGTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCC7GENICheterozygous147550050
792865319286532T7GENICheterozygous403611201
792865319286532TG7GENICheterozygous403611202
792897859289786GA23GENIChomozygous146446232
792900099290010AG28GENIChomozygous146446233
792904749290475GA30GENIChomozygous146446234
792915129291513GA25GENIChomozygous146446235
792922429292243C25GENICheterozygous403611203
792922429292243CT25GENIChomozygous403611204
792922609292261CT27GENIChomozygous146446236
792922739292291TCCTCCTCCTCCTCCTCT26GENIChomozygous146435035
792932509293252AG32GENIChomozygous146435036
792952599295260AG29GENIChomozygous137999911
792923989292399GA30GENIChomozygous146446237
792938229293823CT31GENIChomozygous146446238
792948429294843GA27GENIChomozygous146446239
792953739295374AG31GENIChomozygous146446240
792963709296371CT24GENIChomozygous146446241
792969409296944GCCT19GENIChomozygous146435037
792971819297182GC32GENIChomozygous137999912
792972129297223GTGGACATTGT29GENIChomozygous146435038
792974019297405GTGA16GENIChomozygous146435039