chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 91133094 91133095 C T 4 GENIC homozygous 117068583 10 91134392 91134393 A G 27 GENIC homozygous 116905425 10 91134557 91134558 C T 18 GENIC homozygous 116905427 10 91134900 91134901 T A 19 GENIC homozygous 116905429 10 91135716 91135717 A G 14 GENIC homozygous 116905431 10 91136156 91136157 A G 15 GENIC homozygous 116905433 10 91140303 91140304 A T 20 GENIC homozygous 116905435 10 91140304 91140305 G A 20 GENIC homozygous 116905437 10 91141239 91141240 T C 11 GENIC homozygous 116905439 10 91146554 91146555 T C 20 GENIC homozygous 116905441 10 91147362 91147363 A G 7 GENIC homozygous 116905443 10 91149470 91149471 A G 20 GENIC homozygous 116905445 10 91149559 91149560 A T 17 GENIC homozygous 116905447 10 91149579 91149580 T C 20 GENIC homozygous 116905449 10 91150735 91150736 T C 18 GENIC homozygous 116905451 10 91152040 91152041 C T 14 GENIC homozygous 116905453 10 91157692 91157693 G A 13 GENIC possibly homozygous 116905455 10 91158060 91158061 G T 16 GENIC homozygous 117068585 10 91159672 91159673 T C 12 GENIC homozygous 116905457 10 91159801 91159802 G A 21 GENIC homozygous 116905459 10 91160311 91160312 A G 12 GENIC homozygous 116905461 10 91156112 91156113 G C 5 GENIC homozygous 118007841 10 91140586 91140586 TGAG 13 GENIC homozygous 131708980 10 91147523 91147524 G 27 GENIC homozygous 131708981 10 91153586 91153586 T 16 GENIC homozygous 131708982 10 91155540 91155541 T 20 GENIC homozygous 131708983 10 91157317 91157318 C 6 GENIC homozygous 131708984