chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7110983988110983989A17GENICheterozygous145610086
7110983992110983993A14GENICheterozygous403829792
7110983992110983993AT14GENICheterozygous403829793
7110983995110983996C16GENICheterozygous403932770
7110983995110983996CA16GENICheterozygous403932771
7110983995110983996CG16GENICheterozygous403932772
7110988805110988806GA60GENIChomozygous154482880
7110988805110988806GT60GENICheterozygous154482881
7110984172110984173TC51GENIChomozygous143365593
7110984042110984043CG34GENIChomozygous138182040
7110986921110986922TG94GENIChomozygous138182041
7110987011110987012TC75GENIChomozygous138182042
7110988200110988201GA63GENIChomozygous143365594
7110988488110988488AT64GENIChomozygous137974255
7110991446110991446AAAAAAC15GENICheterozygous146820216
7110991447110991447AAAAAC13GENICheterozygous145610087
7110991460110991461CA18GENIChomozygous143365600
7110991624110991624GAGTCCG54GENIChomozygous143350654
7110992853110992854AT68GENIChomozygous145635019
7110989597110989598CT73GENIChomozygous145635016
7110992401110992402GA56GENIChomozygous145635017
7110992461110992462GA56GENIChomozygous145635018
7110993238110993239GA59GENIChomozygous143365602
7110993243110993244GA59GENIChomozygous143365603
7110996121110996122GA65GENIChomozygous143365605
7110996522110996523CT71GENIChomozygous145635020
7110997109110997110TC58GENIChomozygous143365606
7110997128110997128C56GENIChomozygous145610088
7110997637110997638GA39GENIChomozygous145635021
7110997972110997973GA45GENIChomozygous143365607
7110998064110998065GC17GENIChomozygous141093197
7110998431110998432CT46GENIChomozygous143365609
7110999108110999111CAT43GENIChomozygous145610089
7111000084111000084G46GENIChomozygous143350655
7111000474111000475CG59GENIChomozygous145635022
7111003359111003360TC53GENIChomozygous143365613
7110997548110997549AC36GENICheterozygous403617340
7111005360111005361AG67GENIChomozygous143365615
7111006369111006370AG42GENIChomozygous143365618
7110997548110997549A36GENICpossibly homozygous403617341