chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 118333710 118333711 C G 26 GENIC homozygous 116673621 8 118334459 118334460 C T 32 GENIC homozygous 116673623 8 118335458 118335459 T C 29 GENIC homozygous 116673625 8 118335668 118335669 A T 36 GENIC homozygous 116673627 8 118335683 118335684 C T 36 GENIC homozygous 116673629 8 118336948 118336949 A G 30 GENIC homozygous 116673633 8 118337315 118337316 A G 32 GENIC homozygous 116673635 8 118337419 118337420 C A 29 GENIC homozygous 116673637 8 118338780 118338781 A G 41 GENIC homozygous 116673639 8 118339657 118339658 C T 32 GENIC homozygous 116673641 8 118340453 118340454 A C 33 GENIC homozygous 116673643 8 118340747 118340748 A G 29 GENIC homozygous 116673645 8 118342359 118342360 G T 21 GENIC homozygous 116673647 8 118342391 118342392 A G 23 GENIC homozygous 116673649 8 118342633 118342634 A G 18 GENIC homozygous 116673651 8 118343506 118343507 T C 41 GENIC homozygous 116673653 8 118343771 118343772 A G 26 GENIC homozygous 116673655 8 118345584 118345585 A G 33 GENIC heterozygous 116673657 8 118345587 118345588 T G 30 GENIC heterozygous 116673659 8 118345680 118345681 A G 21 GENIC homozygous 116673661 8 118346242 118346243 G A 36 GENIC homozygous 116673663