chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 25506659 25506660 T C 17 GENIC homozygous 112558959 4 25506894 25506895 A G 9 GENIC homozygous 112558961 4 25507034 25507035 T G 10 GENIC homozygous 112558963 4 25507546 25507547 T C 15 GENIC homozygous 112558965 4 25508256 25508257 C T 11 GENIC homozygous 112558967 4 25508258 25508259 T G 10 GENIC homozygous 112558969 4 25510084 25510085 G A 18 GENIC homozygous 112558971 4 25510404 25510405 A G 9 GENIC homozygous 112558973 4 25510995 25510996 G A 24 GENIC homozygous 112558975 4 25511634 25511635 C A 24 GENIC homozygous 112558977 4 25511702 25511703 A G 23 GENIC homozygous 112558979 4 25512958 25512959 C T 18 GENIC homozygous 112558981 4 25513983 25513984 A G 20 GENIC homozygous 112558983 4 25514011 25514012 A G 26 GENIC homozygous 112558985 4 25515982 25515983 A G 19 GENIC homozygous 112558987 4 25516345 25516346 A G 8 GENIC homozygous 112558989 4 25516445 25516446 C A 17 GENIC homozygous 112558991 4 25517035 25517036 C T 18 GENIC homozygous 112558997 4 25517875 25517876 C T 24 GENIC homozygous 112558999 4 25518396 25518397 C T 19 GENIC homozygous 112559001 4 25518506 25518507 G T 26 GENIC homozygous 112559003 4 25518545 25518546 G A 24 GENIC homozygous 112559005 4 25519071 25519072 C T 23 GENIC homozygous 112559007