chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 84106152 84106153 T 13 GENIC homozygous 129762404 X 84111358 84111389 TACTCTTTACTTAAATGATTATGGAAAATAA 6 GENIC homozygous 129762405 X 84111506 84111507 T G 11 GENIC homozygous 108281391 X 84111507 84111508 G T 11 GENIC homozygous 108281393 X 84123629 84123630 A C 7 GENIC homozygous 108281429 X 84123634 84123635 A T 7 GENIC homozygous 108281431 X 84136394 84136394 TCACCT 9 GENIC homozygous 129762409 X 84140182 84140183 A 3 GENIC homozygous 130611742 X 84139707 84139708 T 1 GENIC homozygous 130611739 X 84139836 84139837 G 3 GENIC homozygous 130611740 X 84139889 84139889 T 2 GENIC homozygous 130611741 X 84162344 84162347 GTA 13 GENIC homozygous 129762417 X 84162363 84162364 G 11 GENIC homozygous 129762418 X 84162366 84162367 G 11 GENIC homozygous 129762419 X 84162370 84162371 G 9 GENIC homozygous 129762420 X 84162373 84162374 A 9 GENIC homozygous 129762421 X 84162381 84162382 G 10 GENIC homozygous 129762422 X 84162393 84162394 G 7 GENIC homozygous 129762423 X 84162405 84162406 G 8 GENIC homozygous 129762424 X 84162414 84162415 G 6 GENIC homozygous 129762425 X 84162423 84162424 A 5 GENIC homozygous 129762426 X 84162348 84162349 G T 13 GENIC homozygous 108596769