chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 117515039 117515040 C T 9 GENIC homozygous 111684555 3 117515460 117515461 T A 33 GENIC homozygous 111684556 3 117516399 117516400 C G 23 GENIC homozygous 111684560 3 117516741 117516742 A G 29 GENIC homozygous 111684563 3 117517214 117517215 G T 28 GENIC homozygous 119887782 3 117517932 117517933 A G 25 GENIC homozygous 111684566 3 117519063 117519064 C T 16 GENIC homozygous 111684568 3 117519851 117519852 C T 27 GENIC homozygous 119887783 3 117520002 117520003 T A 10 GENIC homozygous 119702533 3 117520127 117520128 A G 8 GENIC homozygous 111684570 3 117520353 117520354 G A 18 GENIC homozygous 112294474 3 117521823 117521824 A G 34 GENIC homozygous 112294484 3 117521896 117521897 G T 21 GENIC homozygous 111684574 3 117521958 117521959 T C 25 GENIC homozygous 112020845 3 117521962 117521963 T C 27 GENIC homozygous 112294486 3 117522786 117522787 G C 36 GENIC homozygous 111684576 3 117523221 117523222 A G 33 GENIC homozygous 119887784 3 117523466 117523467 G T 22 GENIC homozygous 111684578 3 117523866 117523867 A G 16 GENIC homozygous 111684579 3 117524461 117524462 T C 21 GENIC homozygous 111684580 3 117525045 117525046 A G 22 GENIC homozygous 111684581