chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 89687468 89687469 A T 6 GENIC homozygous 116820861 10 89687532 89687533 A G 6 GENIC homozygous 116820865 10 89688154 89688155 A G 16 GENIC homozygous 116820869 10 89688635 89688636 T C 16 GENIC homozygous 116820871 10 89689442 89689443 T C 6 GENIC homozygous 116820873 10 89690317 89690318 A G 13 GENIC homozygous 116820875 10 89691227 89691228 C T 19 GENIC homozygous 116902927 10 89692446 89692447 A C 11 GENIC homozygous 116902929 10 89692644 89692645 G A 15 GENIC homozygous 116820879 10 89694360 89694361 A T 9 GENIC homozygous 116982537 10 89694581 89694582 T C 21 GENIC homozygous 116820891 10 89694927 89694928 G A 20 GENIC possibly homozygous 116902931 10 89695435 89695436 A T 16 GENIC homozygous 116902933 10 89695475 89695476 C G 4 GENIC homozygous 116902934 10 89695726 89695727 C T 9 GENIC homozygous 116902936 10 89695856 89695857 T C 6 GENIC homozygous 116820893 10 89696334 89696335 A G 26 GENIC homozygous 116902940 10 89696412 89696413 A G 19 GENIC homozygous 116820895 10 89697045 89697046 C T 4 GENIC homozygous 116902942 10 89697803 89697804 G A 5 GENIC homozygous 126476321 10 89697805 89697806 G A 5 GENIC heterozygous 126476322