chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7110983988110983989A6GENIChomozygous145610086
7110983992110983993A6GENIChomozygous403829792
7110983992110983993AT6GENICheterozygous403829793
7110983995110983996C6GENICheterozygous403932770
7110983995110983996CA6GENICheterozygous403932771
7110983995110983996CG6GENIChomozygous403932772
7110987011110987012TC21GENIChomozygous138182042
7110984172110984173TC33GENIChomozygous143365593
7110988200110988201GA25GENIChomozygous143365594
7110984042110984043CG10GENIChomozygous138182040
7110986921110986922TG18GENIChomozygous138182041
7110988805110988806GA28GENIChomozygous154482880
7110988805110988806GT28GENICheterozygous154482881
7110991447110991447AAAAAC14GENICpossibly homozygous145610087
7110991460110991461CA13GENIChomozygous143365600
7110993238110993239GA24GENIChomozygous143365602
7110993243110993244GA24GENIChomozygous143365603
7110996121110996122GA24GENIChomozygous143365605
7110997109110997110TC24GENIChomozygous143365606
7110997128110997128C24GENIChomozygous145610088
7110997972110997973GA14GENIChomozygous143365607
7110998431110998432CT25GENIChomozygous143365609
7110999108110999111CAT12GENIChomozygous145610089
7110989597110989598CT26GENIChomozygous145635016
7110992401110992402GA29GENIChomozygous145635017
7110992461110992462GA30GENIChomozygous145635018
7110992853110992854AT28GENIChomozygous145635019
7110996522110996523CT27GENIChomozygous145635020
7110997637110997638GA14GENIChomozygous145635021
7111000474111000475CG13GENIChomozygous145635022
7110991624110991624GAGTCCG20GENIChomozygous143350654
7111000084111000084G14GENIChomozygous143350655
7110997548110997549AC13GENICheterozygous403617340
7110997548110997549A13GENIChomozygous403617341
7110998064110998065GC6GENIChomozygous141093197
7111003359111003360TC18GENIChomozygous143365613
7111005360111005361AG18GENIChomozygous143365615
7111006369111006370AG10GENIChomozygous143365618
7110988488110988488AT30GENIChomozygous137974255