chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 65376727 65376728 G A 27 GENIC possibly homozygous 783298611 X 65386337 65386338 G A 77 GENIC heterozygous 783298612 X 65386346 65386347 C T 70 GENIC heterozygous 783298613 X 65386352 65386353 G A 78 GENIC heterozygous 783298614 X 65386419 65386420 T A 82 GENIC heterozygous 783298615 X 65386483 65386484 A T 36 GENIC heterozygous 783298616 X 65387998 65387999 T G 19 GENIC homozygous 783298617 X 65388009 65388010 T G 18 GENIC homozygous 783298618 X 65388034 65388035 C A 10 GENIC homozygous 783298619 X 65390779 65390780 G T 132 GENIC heterozygous 783298620 X 65390812 65390813 A G 171 GENIC heterozygous 783298621 X 65390836 65390837 A T 234 GENIC heterozygous 783298622 X 65393956 65393957 G A 47 GENIC homozygous 783298623 X 65394268 65394269 T A 44 GENIC possibly homozygous 783298624 X 65394962 65394963 G A 100 GENIC heterozygous 783298625 X 65395038 65395039 A G 94 GENIC heterozygous 783298626 X 65395446 65395447 A G 97 GENIC heterozygous 783298627 X 65395512 65395513 C G 92 GENIC heterozygous 783298628 X 65395559 65395560 T A 115 GENIC heterozygous 783298629