chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 153682679 153682680 T C 46 GENIC homozygous 114057834 5 153685371 153685372 T C 29 GENIC homozygous 114057842 5 153686032 153686033 C A 19 GENIC homozygous 114057846 5 153686034 153686035 C A 22 GENIC homozygous 114057848 5 153686051 153686052 C A 30 GENIC homozygous 114057850 5 153686054 153686055 C A 31 GENIC homozygous 114057852 5 153686061 153686062 C A 38 GENIC homozygous 114057854 5 153686138 153686139 T C 56 GENIC homozygous 114057856 5 153686186 153686187 C A 37 GENIC possibly homozygous 114157370 5 153690486 153690487 A C 64 GENIC possibly homozygous 114157371 5 153693180 153693181 C T 50 GENIC homozygous 114157372 5 153695545 153695546 A G 62 GENIC homozygous 114057874 5 153695714 153695715 C A 64 GENIC possibly homozygous 114157373 5 153695737 153695738 C T 64 GENIC homozygous 114057876 5 153697767 153697768 G A 45 GENIC homozygous 114057878 5 153703304 153703305 G T 51 GENIC possibly homozygous 114157374 5 153704160 153704161 C G 67 GENIC homozygous 114157375 5 153706069 153706070 C T 57 GENIC homozygous 114157376