chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5126032086126032087CA23GENIChomozygous113996234
5126033190126033191CT21GENIChomozygous119016563
5126033195126033196AC20GENIChomozygous114137061
5126033288126033289AG24GENIChomozygous119016564
5126033315126033316AG29GENIChomozygous114137062
5126033452126033453TC24GENIChomozygous113996238
5126036930126036931CT21GENIChomozygous119016565
5126038193126038194CT18GENIChomozygous119016566
5126039815126039816CT19GENIChomozygous119016568
5126040091126040092AG26GENIChomozygous119016569
5126040408126040409GA12GENIChomozygous119016570
5126041315126041316AG21GENIChomozygous113996244
5126042900126042901TC13GENIChomozygous113996248
5126043317126043318GA28GENIChomozygous119016571
5126044095126044096GA31GENIChomozygous119016572
5126045272126045273CA27GENIChomozygous119016573
5126047001126047002TC22GENIChomozygous119016574
5126047385126047386CT26GENIChomozygous119016575
5126047440126047441TG25GENIChomozygous119016576
5126047794126047795GA23GENIChomozygous119016577
5126047821126047822TA26GENIChomozygous113996250
5126039256126039256T16GENIChomozygous132843574
5126049729126049730A19GENIChomozygous132843575
5126050324126050325GA14GENIChomozygous113996254
5126050356126050357GA11GENIChomozygous113996256
5126050683126050684TG19GENIChomozygous113996258
5126051044126051045GT13GENIChomozygous119016578
5126051281126051282GA21GENIChomozygous113996260
5126052153126052154A14GENIChomozygous128235370
5126053516126053517GT21GENIChomozygous113996262