chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 100291857 100291858 T 50 GENIC homozygous 137700512 6 100295567 100295568 T G 65 GENIC homozygous 137862686 6 100295736 100295737 C G 57 GENIC homozygous 137862687 6 100302444 100302444 A 47 GENIC possibly homozygous 137700514 6 100303272 100303273 C T 67 GENIC homozygous 137862688 6 100303302 100303303 A G 65 GENIC homozygous 137862689 6 100305296 100305297 C A 49 GENIC homozygous 137862690 6 100305855 100305856 C T 37 GENIC homozygous 137862691 6 100305860 100305863 TCC 33 GENIC homozygous 137700515 6 100313161 100313161 CTCCCCTCATGG 57 GENIC homozygous 137700516 6 100318430 100318431 T 36 GENIC homozygous 137700517 6 100318679 100318679 TGTGTA 38 GENIC possibly homozygous 137700518 6 100320701 100320702 T A 52 GENIC homozygous 137862692 6 100320932 100320933 T C 67 GENIC homozygous 137862693 6 100321626 100321627 T C 64 GENIC homozygous 137862694 6 100322790 100322791 C T 51 GENIC homozygous 137862695 6 100323384 100323384 T 59 GENIC homozygous 137700519 6 100323731 100323732 G A 55 GENIC homozygous 137862696 6 100325993 100325994 A G 67 GENIC homozygous 137862697 6 100328257 100328258 T G 47 GENIC homozygous 137862698 6 100328685 100328686 G A 52 GENIC homozygous 137862699 6 100318681 100318681 TGTA 42 GENIC heterozygous 144749691