chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 44503101 44503102 C T 19 GENIC possibly homozygous 563835122 8 44503212 44503213 T TA 6 GENIC homozygous 708444834 8 44503247 44503248 T C 17 GENIC possibly homozygous 563835123 8 44504328 44504329 G GA 10 GENIC heterozygous 708444836 8 44504674 44504675 T C 17 GENIC possibly homozygous 563835124 8 44505305 44505306 A G 17 GENIC homozygous 563835125 8 44506607 44506608 C T 20 GENIC possibly homozygous 565263964 8 44507106 44507107 T C 9 GENIC possibly homozygous 563835126 8 44507925 44507926 T C 7 GENIC homozygous 563835127 8 44509560 44509561 G A 16 GENIC homozygous 563835128 8 44509572 44509573 G T 13 GENIC homozygous 565263965 8 44509926 44509927 G C 26 GENIC possibly homozygous 563835129 8 44510062 44510063 G A 12 GENIC homozygous 563835130 8 44510207 44510208 T C 15 GENIC homozygous 565263966 8 44510763 44510764 G A 20 GENIC homozygous 565263967 8 44511737 44511738 A G 20 GENIC possibly homozygous 563835131 8 44512920 44512921 A T 30 GENIC possibly homozygous 565263968 8 44513286 44513287 A C 7 GENIC homozygous 563835132 8 44513630 44513631 T A 13 GENIC heterozygous 563835133 8 44513766 44513767 C CA 2 GENIC homozygous 708444837 8 44515042 44515043 T C 20 GENIC homozygous 563835134 8 44515128 44515129 G A 14 GENIC homozygous 563835135 8 44516537 44516538 A T 16 GENIC homozygous 563835136