chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5139694279139694280AC71GENIChomozygous780334356
5139694442139694443GA60GENIChomozygous780334357
5139695215139695216CT59GENICheterozygous780334358
5139696549139696550AG50GENIChomozygous780334359
5139700094139700095CT62GENIChomozygous780334360
5139701742139701743TC55GENIChomozygous780334361
5139705291139705292GA68GENIChomozygous780334362
5139705551139705552GT46GENIChomozygous780334363
5139708988139708989CA49GENICpossibly homozygous780334364
5139709936139709937CT59GENIChomozygous780334365
5139711213139711214GA76GENIChomozygous780334366
5139713601139713602AT33GENICheterozygous780334367
5139713655139713656GA45GENICheterozygous780334368
5139717005139717006GA60GENIChomozygous780334369
5139724327139724328TA68GENIChomozygous780334370
5139726010139726011GT16GENIChomozygous780334371
5139727912139727913TA34GENIChomozygous780334372
5139733451139733452AG77GENIChomozygous780334373
5139733937139733938AC39GENIChomozygous780334374
5139734191139734192TC60GENIChomozygous780334375
5139736164139736165CT58GENIChomozygous780334376
5139738095139738096GA42GENICpossibly homozygous780334377