chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 26011096 26011097 C T 33 GENIC homozygous 504306577 20 26013435 26013436 C T 16 GENIC homozygous 504306578 20 26013704 26013705 A G 21 GENIC homozygous 504306579 20 26014288 26014289 C T 53 GENIC homozygous 504306580 20 26014454 26014455 C T 56 GENIC possibly homozygous 504306581 20 26015254 26015255 A G 58 GENIC homozygous 504306582 20 26015400 26015401 C T 37 GENIC homozygous 504306583 20 26015543 26015544 A T 27 GENIC homozygous 504306584 20 26016565 26016566 G A 49 GENIC homozygous 504306585 20 26017120 26017121 C G 59 GENIC homozygous 504306586 20 26017288 26017289 T - 22 GENIC homozygous 684978513 20 26017377 26017378 C T 30 GENIC homozygous 503338690 20 26017560 26017561 T G 30 GENIC heterozygous 504306587 20 26017882 26017883 T - 24 GENIC homozygous 684978514 20 26017949 26017950 C T 39 GENIC possibly homozygous 504306588 20 26018041 26018042 C T 44 GENIC homozygous 504306589 20 26018255 26018256 T TAAA 26 GENIC homozygous 684978516 20 26018466 26018467 C G 52 GENIC homozygous 504306590 20 26018719 26018720 T C 23 GENIC homozygous 504306591 20 26018836 26018837 C CTT 31 GENIC homozygous 684978517 20 26019064 26019065 T C 41 GENIC homozygous 504306592 20 26019278 26019279 T C 30 GENIC homozygous 504306593 20 26019638 26019639 G A 30 GENIC homozygous 504306594 20 26019870 26019871 T - 21 GENIC homozygous 684978518 20 26020191 26020192 A - 40 GENIC homozygous 684978519