chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 84482942 84482943 G T 15 GENIC possibly homozygous 113605956 14 84483248 84483249 A G 14 GENIC possibly homozygous 113605957 14 84483552 84483552 TGACAG 10 GENIC homozygous 131145626 14 84484516 84484516 T 7 GENIC homozygous 131145627 14 84484866 84484867 T C 10 GENIC homozygous 113605958 14 84484887 84484887 CCACTGAGCCATCTCCCCACTGAGCCATCTCC 5 GENIC homozygous 131730838 14 84485884 84485885 C T 13 GENIC homozygous 113605959 14 84486606 84486608 AG 10 GENIC homozygous 131145631 14 84487169 84487170 T C 9 GENIC homozygous 113605960 14 84487269 84487270 G A 12 GENIC homozygous 113605961 14 84487724 84487725 G A 13 GENIC homozygous 113605962 14 84489090 84489091 A G 12 GENIC homozygous 113605963 14 84489680 84489681 T C 18 GENIC homozygous 113605964 14 84489902 84489903 A G 10 GENIC homozygous 113605965 14 84490080 84490081 A G 9 GENIC homozygous 113605966 14 84492488 84492489 T C 11 GENIC homozygous 113605967 14 84492613 84492613 C 8 GENIC homozygous 131145632 14 84493200 84493200 G 10 GENIC homozygous 131145633 14 84494511 84494512 A T 13 GENIC homozygous 113605968 14 84495230 84495231 G A 12 GENIC homozygous 113605969 14 84483611 84483612 T A 13 GENIC possibly homozygous 113680161 14 84485826 84485827 C T 12 GENIC homozygous 113680163 14 84486569 84486570 A G 7 GENIC homozygous 113680165 14 84484318 84484319 T C 7 GENIC homozygous 118766041 14 84496561 84496562 G A 13 GENIC homozygous 113605970 14 84498393 84498394 C T 10 GENIC homozygous 113605971 14 84498538 84498539 G C 20 GENIC homozygous 113680167 14 84498563 84498564 A T 21 GENIC homozygous 113605972 14 84499683 84499684 A C 9 GENIC homozygous 113605973 14 84498535 84498536 G 20 GENIC homozygous 130141496