chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
193676688236766883CT17GENICpossibly homozygous46109418
193676713236767133CT30GENIChomozygous46109420
193676758236767583AG6GENIChomozygous46109422
193676775236767754TT--2GENICheterozygous46109424
193676948336769484GGA8GENICpossibly homozygous46109434
193676950336769504AAG1GENIChomozygous46109436
193676954036769541CA8GENIChomozygous46380047
193676954136769542AC8GENIChomozygous46380049
193676955336769554AG11GENIChomozygous46109438
193676958336769584C-12GENIChomozygous46109440
193676961136769612TA9GENIChomozygous46109442
193676961536769616GGC9GENIChomozygous46109444
193677254036772541CCTA14GENIChomozygous46109445
193677622436776225TTCA2GENIChomozygous46109449