chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107408330474083305AG21GENIChomozygous117369023
107408396174083962TC46GENIChomozygous116636257
107408555074085551GC34GENIChomozygous116636259
107408587474085875CT10GENIChomozygous117256931
107408743274087433CT24GENIChomozygous117256933
107408854674088547AG23GENIChomozygous117278375
107409153974091540TA18GENIChomozygous116636269
107409182774091828GA32GENIChomozygous117278377
107409329774093298CT30GENIChomozygous117256935
107409350374093504TG33GENIChomozygous117256937
107409390874093909AG28GENIChomozygous116636279
107409432974094330CT21GENIChomozygous117256939
107409659274096593TC21GENIChomozygous117256941
107410123574101236TC30GENIChomozygous117256943
107410204574102046AG34GENIChomozygous117256945
107410241574102416AG29GENIChomozygous117256947
107410373574103736CT24GENIChomozygous116636295
107410375974103760CT25GENIChomozygous117256949
107410623774106238CT16GENIChomozygous117256951
107410758174107582CT46GENIChomozygous116636305
107410901474109015AG20GENIChomozygous116636309
107410958074109581CT22GENIChomozygous117256953
107410971174109712CT36GENIChomozygous117256955
107411233174112332AC24GENIChomozygous116636315
107411321374113214CA27GENIChomozygous117256959
107411441174114412TC28GENIChomozygous117256963
107411470474114705TC29GENIChomozygous116636325
107411483174114832GA35GENIChomozygous117256965
107411555974115560GT25GENIChomozygous116636327
107411568074115681GA30GENIChomozygous117256967
107411599074115991GA21GENIChomozygous116636329
107411607074116071TC31GENIChomozygous116636331
107411670774116708TC33GENIChomozygous116636335
107411783574117836AG20GENIChomozygous116636337
107411806174118062TC33GENIChomozygous116636341
107411848574118486GA18GENIChomozygous117256969
107411850474118505TC12GENIChomozygous116636343
107411889674118897CT4GENIChomozygous117278383