chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7106598277106598278TG28GENIChomozygous146200265
7106598531106598532GC24GENIChomozygous146200266
7106598709106598710GT29GENIChomozygous146200267
7106599137106599138CG33GENIChomozygous146200268
7106599549106599562GCCAACCCAGAAT32GENIChomozygous146186080
7106599647106599648GA29GENIChomozygous146200269
7106599716106599717TC29GENIChomozygous146200270
7106599814106599815GA35GENIChomozygous146200271
7106600118106600119GA30GENIChomozygous146200272
7106600249106600250AC30GENIChomozygous138174145
7106601350106601350GT17GENIChomozygous146186081
7106601438106601439CA20GENICpossibly homozygous146200273
7106602197106602198TG33GENIChomozygous146200274
7106602221106602222CT31GENIChomozygous146200275
7106602254106602255TC27GENIChomozygous146200276
7106602255106602256GA27GENIChomozygous146200277
7106602915106602916TC18GENIChomozygous146200278
7106602930106602931AT18GENIChomozygous138174146
7106602931106602932AC18GENIChomozygous138174147