chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 3352328 3352329 A G 25 GENIC homozygous 109068574 20 3352563 3352564 C G 28 GENIC homozygous 109417080 20 3352565 3352566 A G 27 GENIC homozygous 109068576 20 3352965 3352966 T C 34 GENIC homozygous 109417082 20 3353460 3353461 G C 25 GENIC homozygous 109417084 20 3353717 3353718 G T 7 GENIC homozygous 109417086 20 3353980 3353981 C T 24 GENIC homozygous 109417088 20 3354031 3354032 T C 29 GENIC homozygous 109068580 20 3354607 3354608 G A 25 GENIC homozygous 109417090 20 3355294 3355295 G C 29 GENIC homozygous 109417092 20 3355543 3355544 T C 28 GENIC homozygous 109417094 20 3356715 3356716 G A 35 GENIC homozygous 109417096 20 3357216 3357217 C T 23 GENIC homozygous 109417098 20 3357227 3357228 G C 25 GENIC homozygous 109417100 20 3357593 3357594 A G 18 GENIC homozygous 109068587 20 3358982 3358983 T C 21 GENIC homozygous 109417102 20 3359255 3359256 C T 21 GENIC homozygous 109417104 20 3359303 3359304 T C 25 GENIC possibly homozygous 109417106 20 3359435 3359436 G T 16 GENIC homozygous 109068589 20 3360270 3360271 G A 25 GENIC homozygous 109417108 20 3360752 3360753 G A 20 GENIC homozygous 109417110 20 3361134 3361135 A C 19 GENIC homozygous 109417112 20 3361438 3361439 G C 26 GENIC homozygous 109417114 20 3361865 3361866 G A 22 GENIC homozygous 109417116 20 3362716 3362717 A G 13 GENIC homozygous 109417118 20 3362950 3362951 T C 24 GENIC homozygous 109068593 20 3364187 3364188 T C 33 GENIC homozygous 109388931