chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 128027968 128027969 G A 16 GENIC possibly homozygous 53369406 8 128028359 128028360 T C 24 GENIC homozygous 52884672 8 128029653 128029654 C CTT 1 GENIC homozygous 52884674 8 128029841 128029842 C CT 3 GENIC heterozygous 53369407 8 128030349 128030350 C T 15 GENIC possibly homozygous 53369408 8 128030446 128030447 T C 22 GENIC possibly homozygous 52884679 8 128030834 128030835 T C 19 GENIC possibly homozygous 53369409 8 128031132 128031133 G A 32 GENIC homozygous 52884680 8 128031266 128031267 C T 24 GENIC homozygous 53369410 8 128031815 128031816 A AT 2 GENIC heterozygous 53369411 8 128031880 128031881 C T 21 GENIC homozygous 53369412 8 128032311 128032312 A G 10 GENIC homozygous 53233191 8 128032317 128032318 A G 9 GENIC homozygous 53233193 8 128032455 128032456 T A 24 GENIC possibly homozygous 53369413 8 128032496 128032497 C T 19 GENIC heterozygous 53369414 8 128033282 128033283 C T 20 GENIC possibly homozygous 53233196 8 128033386 128033387 C G 21 GENIC possibly homozygous 53369415 8 128033491 128033492 C A 19 GENIC homozygous 53369416 8 128034171 128034172 G A 17 GENIC homozygous 53369417 8 128034308 128034309 A G 14 GENIC homozygous 53369418 8 128034574 128034575 G C 23 GENIC homozygous 53369419 8 128035010 128035011 T - 9 GENIC possibly homozygous 53369420 8 128035400 128035401 A AC 4 GENIC heterozygous 52884694 8 128035473 128035474 G A 22 GENIC homozygous 52884696 8 128035655 128035656 T TG 8 GENIC homozygous 53369421 8 128036381 128036382 C T 17 GENIC homozygous 53369422