chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
86763681767636817TTATAGTATCCCGC47GENIChomozygous146464083
86763706167637062TG49GENIChomozygous147271166
86763908467639085CT29GENIChomozygous147271167
86763988167639882GA64GENIChomozygous147271168
86764006167640064TTG33GENIChomozygous146464084
86764188967641890CT42GENIChomozygous147271169
86764273167642732CA48GENICpossibly homozygous147271170
86764304467643044T43GENICheterozygous144389669
86764648067646480A36GENICpossibly homozygous147265822
86764895367648955TG36GENIChomozygous146464086
86764920867649209TC52GENIChomozygous146473320
86765144967651454AGATC54GENIChomozygous147265823
86765423067654230G50GENIChomozygous147265824
86765666767656668GA73GENIChomozygous147271171
86765968467659685CT38GENIChomozygous147271172
86766006367660064CT31GENIChomozygous147271173