chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 44503101 44503102 C T 16 GENIC homozygous 631549782 8 44503212 44503213 T TA 12 GENIC homozygous 745695172 8 44503247 44503248 T C 20 GENIC homozygous 631549783 8 44504328 44504329 G GA 14 GENIC heterozygous 745695174 8 44504674 44504675 T C 28 GENIC possibly homozygous 631549784 8 44505305 44505306 A G 18 GENIC heterozygous 631549785 8 44506607 44506608 C T 12 GENIC possibly homozygous 631549786 8 44507106 44507107 T C 5 GENIC homozygous 631549787 8 44507925 44507926 T C 7 GENIC homozygous 631549788 8 44509560 44509561 G A 13 GENIC homozygous 631549789 8 44509572 44509573 G T 9 GENIC homozygous 631549790 8 44509926 44509927 G C 17 GENIC homozygous 631549791 8 44510062 44510063 G A 20 GENIC homozygous 631549792 8 44510207 44510208 T C 11 GENIC heterozygous 631549793 8 44510763 44510764 G A 20 GENIC homozygous 631549794 8 44511737 44511738 A G 30 GENIC possibly homozygous 631549795 8 44512920 44512921 A T 22 GENIC possibly homozygous 631549796 8 44513124 44513128 TTTA ---- 2 GENIC homozygous 745695175 8 44513286 44513287 A C 14 GENIC homozygous 631549797 8 44513630 44513631 T A 12 GENIC heterozygous 631549798 8 44515042 44515043 T C 17 GENIC homozygous 631549799 8 44515128 44515129 G A 28 GENIC possibly homozygous 631549800 8 44516537 44516538 A T 20 GENIC homozygous 631549801