chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 131837546 131837547 G A 27 GENIC homozygous 812158991 5 131844777 131844778 G A 39 GENIC homozygous 812158992 5 131845402 131845403 C T 31 GENIC homozygous 812158993 5 131845727 131845728 C A 26 GENIC homozygous 812158994 5 131846180 131846181 T G 19 GENIC homozygous 812158995 5 131847859 131847860 G A 34 GENIC homozygous 812158996 5 131848908 131848909 T G 18 GENIC homozygous 812158997 5 131849903 131849904 G A 13 GENIC homozygous 812158998 5 131850089 131850090 A T 19 GENIC homozygous 812158999 5 131850416 131850417 T C 11 GENIC homozygous 812159000 5 131853410 131853411 A G 35 GENIC homozygous 812159001 5 131853511 131853512 T G 21 GENIC homozygous 812159002 5 131853678 131853679 T C 29 GENIC homozygous 812159003 5 131859483 131859484 T C 21 GENIC homozygous 812159004 5 131859936 131859937 G A 33 GENIC homozygous 812159005 5 131862290 131862291 C G 33 GENIC homozygous 812159006