chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 111698989 111698990 G A 11 GENIC homozygous 116648596 8 111700490 111700491 T C 21 GENIC homozygous 116648598 8 111700575 111700576 T C 24 GENIC homozygous 116648600 8 111702284 111702285 G A 25 GENIC homozygous 116648603 8 111706168 111706169 G A 14 GENIC homozygous 116648605 8 111706234 111706235 G A 16 GENIC homozygous 116648607 8 111706261 111706262 G A 14 GENIC homozygous 116648609 8 111706952 111706953 C T 11 GENIC homozygous 116648611 8 111708179 111708180 G A 21 GENIC homozygous 116648613 8 111708481 111708482 T C 20 GENIC homozygous 116648615 8 111709172 111709173 G C 30 GENIC homozygous 116648617 8 111709376 111709377 G A 26 GENIC homozygous 116648619 8 111710507 111710508 A T 15 GENIC possibly homozygous 116648621 8 111711762 111711763 G T 18 GENIC homozygous 116648623 8 111713977 111713978 A G 26 GENIC homozygous 116648627 8 111714595 111714596 A G 20 GENIC homozygous 116648629 8 111716278 111716279 T G 21 GENIC homozygous 116648631 8 111717640 111717641 G A 22 GENIC homozygous 116648633 8 111719885 111719886 A G 21 GENIC homozygous 116648637 8 111720114 111720115 G A 24 GENIC homozygous 116648639 8 111720827 111720828 C T 12 GENIC homozygous 116648641