chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 262091859 262091860 A - 19 GENIC possibly homozygous 59540165 2 262092325 262092326 T C 11 GENIC homozygous 59540170 2 262092432 262092433 T TAAGA 5 GENIC homozygous 61219050 2 262093549 262093550 C - 20 GENIC homozygous 59540185 2 262094436 262094437 A - 1 GENIC homozygous 60553407 2 262095083 262095084 C CA 7 GENIC heterozygous 59540193 2 262095084 262095085 A - 7 GENIC heterozygous 59972181 2 262097197 262097198 T A 21 GENIC heterozygous 59540223 2 262097636 262097637 T C 19 GENIC homozygous 59540224 2 262097695 262097696 C T 24 GENIC homozygous 60090709 2 262098078 262098079 T C 30 GENIC homozygous 59540228 2 262098842 262098843 C T 25 GENIC homozygous 60090710 2 262098947 262098948 C T 10 GENIC homozygous 60090711 2 262099073 262099074 G A 6 GENIC homozygous 60090712 2 262099623 262099624 A ATTT 16 GENIC homozygous 60090713 2 262099965 262099966 C A 21 GENIC homozygous 59540237 2 262100021 262100022 T TC 23 GENIC homozygous 59540238 2 262100024 262100025 T G 23 GENIC homozygous 60465033 2 262100719 262100720 C T 30 GENIC possibly homozygous 60090715 2 262100868 262100869 T C 29 GENIC possibly homozygous 60090716 2 262100912 262100913 G T 27 GENIC homozygous 59540246 2 262101180 262101181 T G 27 GENIC homozygous 59540247 2 262101278 262101279 C A 16 GENIC homozygous 60090717 2 262101315 262101316 C T 17 GENIC homozygous 60090718 2 262101452 262101453 A G 13 GENIC homozygous 59540249 2 262101650 262101653 TTT --- 16 GENIC homozygous 60090719 2 262101958 262101959 T C 22 GENIC homozygous 59540255 2 262102094 262102095 G GA 9 GENIC homozygous 61219052 2 262102154 262102155 A G 30 GENIC homozygous 59540256 2 262102844 262102845 G - 32 GENIC homozygous 60090721