chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 126901949 126901950 G A 17 GENIC homozygous 119409587 4 126905311 126905312 C T 15 GENIC homozygous 119409588 4 126905371 126905372 T G 18 GENIC homozygous 113302650 4 126906203 126906204 C T 15 GENIC homozygous 119409589 4 126908259 126908260 G A 11 GENIC homozygous 119409590 4 126908783 126908784 C G 9 GENIC heterozygous 126132418 4 126909404 126909405 A C 25 GENIC homozygous 119409591 4 126911666 126911667 T C 12 GENIC homozygous 113302663 4 126913301 126913302 T C 8 GENIC homozygous 119409592 4 126913889 126913890 A G 26 GENIC homozygous 113302669 4 126921865 126921866 A G 26 GENIC homozygous 113302673 4 126922472 126922473 A G 15 GENIC homozygous 113302676 4 126923977 126923978 A G 18 GENIC homozygous 113302680 4 126924062 126924063 A G 13 GENIC homozygous 113302681 4 126924285 126924286 C T 5 GENIC homozygous 119409593 4 126924291 126924292 T C 9 GENIC homozygous 119409594 4 126927626 126927627 T C 11 GENIC homozygous 119409595