chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 131842186 131842187 A C 20 GENIC homozygous 932214884 5 131842813 131842814 G A 16 GENIC homozygous 932214885 5 131844777 131844778 G A 13 GENIC homozygous 932214886 5 131845402 131845403 C T 7 GENIC homozygous 932214887 5 131845727 131845728 C A 11 GENIC homozygous 932214888 5 131846180 131846181 T G 9 GENIC homozygous 932214889 5 131850416 131850417 T C 4 GENIC homozygous 932214890 5 131852932 131852933 C A 8 GENIC homozygous 932214891 5 131853410 131853411 A G 11 GENIC homozygous 932214892 5 131853511 131853512 T G 9 GENIC homozygous 932214893 5 131853678 131853679 T C 13 GENIC homozygous 932214894 5 131854297 131854298 C A 8 GENIC homozygous 932214895 5 131855380 131855381 C G 11 GENIC homozygous 932214896 5 131859483 131859484 T C 10 GENIC homozygous 932214897 5 131859936 131859937 G A 15 GENIC homozygous 932214898 5 131861443 131861444 G T 10 GENIC homozygous 932214899 5 131862290 131862291 C G 12 GENIC homozygous 932214900 5 131864052 131864053 C T 11 GENIC homozygous 932214901