chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 15969785 15969786 C CAT 16 GENIC possibly homozygous 694932572 20 15969814 15969816 AC -- 8 GENIC homozygous 694932573 20 15969872 15969873 T TAC 16 GENIC homozygous 694932574 20 15970091 15970092 T TACAC 8 GENIC homozygous 694932575 20 15970467 15970468 G GCGCGCACA 11 GENIC possibly homozygous 694932578 20 15970575 15970576 T C 25 GENIC homozygous 530960433 20 15970698 15970699 A G 37 GENIC homozygous 530960434 20 15970777 15970778 C T 26 GENIC homozygous 530960435 20 15971014 15971015 A G 24 GENIC homozygous 530960436 20 15971113 15971114 C - 14 GENIC homozygous 694932580 20 15971164 15971165 C T 28 GENIC homozygous 530960437 20 15971344 15971345 A G 32 GENIC homozygous 530960438 20 15971529 15971530 T C 28 GENIC homozygous 530960439 20 15971806 15971807 C - 25 GENIC homozygous 694932581 20 15972036 15972037 C G 21 GENIC homozygous 530960440 20 15972387 15972388 G A 31 GENIC homozygous 530960441 20 15972612 15972613 C CTT 21 GENIC homozygous 694932582 20 15972968 15972969 C T 24 GENIC homozygous 530960442 20 15973391 15973392 G C 16 GENIC homozygous 530960443 20 15973706 15973707 A - 14 GENIC homozygous 694932583 20 15973783 15973784 G A 18 GENIC homozygous 530960444 20 15973789 15973790 C A 19 GENIC homozygous 530960445 20 15974734 15974735 A G 22 GENIC homozygous 530960446