chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 84041901 84041902 G A 29 GENIC homozygous 116069066 11 84042146 84042147 A G 26 GENIC homozygous 116069068 11 84042198 84042199 A G 24 GENIC possibly homozygous 116069071 11 84043119 84043120 C T 29 GENIC homozygous 116069073 11 84043127 84043128 C T 33 GENIC homozygous 116069075 11 84043941 84043942 A G 5 GENIC homozygous 116207739 11 84044072 84044073 G A 21 GENIC homozygous 116069077 11 84044170 84044171 G C 35 GENIC homozygous 116069079 11 84044171 84044172 G C 36 GENIC homozygous 116069081 11 84044202 84044203 C G 31 GENIC homozygous 116069083 11 84044934 84044935 T A 20 GENIC homozygous 116069085 11 84045112 84045113 G C 10 GENIC homozygous 116069087 11 84046037 84046038 A G 31 GENIC homozygous 116069089 11 84046183 84046184 T G 12 GENIC homozygous 116069091 11 84046487 84046488 C T 29 GENIC homozygous 116069093 11 84046688 84046689 A T 8 GENIC homozygous 116207741 11 84046692 84046693 A T 7 GENIC homozygous 116207743 11 84047391 84047392 C T 20 GENIC homozygous 116069095 11 84047408 84047409 C G 23 GENIC homozygous 116207745