chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15106650923106650924G-1GENIChomozygous693092008
15106661143106661144CT29GENIChomozygous527478846
15106671680106671681AG31GENIChomozygous527478847
15106671787106671788TG22GENIChomozygous527478848
15106673001106673002AAG29GENIChomozygous693092009
15106673263106673264CT22GENICpossibly homozygous527478849
15106673272106673273TC22GENICheterozygous527478850
15106674392106674394GT--28GENICpossibly homozygous693092011
15106674521106674522CT29GENIChomozygous524848899
15106674601106674603TG--34GENIChomozygous693092012
15106674681106674683TG--24GENIChomozygous693092013
15106674818106674819AATG40GENIChomozygous693092014
15106675096106675097CCT29GENIChomozygous693092015
15106675479106675480AG29GENICheterozygous527478851
15106675483106675484TG31GENICheterozygous527478852
15106676202106676205TAA---19GENICheterozygous693092016
15106678508106678509GGA21GENIChomozygous693092017
15106679194106679195G-23GENIChomozygous693092018
15106679632106679633TTTCTC2GENIChomozygous693092019
15106681105106681106GC52GENIChomozygous527478853