chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 103266002 103266003 C T 8 GENIC homozygous 139612445 14 103266646 103266647 G A 14 GENIC homozygous 139612446 14 103267745 103267746 A G 9 GENIC homozygous 139612447 14 103267979 103267980 A G 7 GENIC homozygous 140915390 14 103268010 103268011 A G 5 GENIC homozygous 140915391 14 103269190 103269191 G A 12 GENIC homozygous 139612448 14 103269256 103269257 A G 16 GENIC homozygous 139612449 14 103269819 103269828 ATTCAGTGT 15 GENIC homozygous 139414619 14 103270038 103270039 C G 20 GENIC homozygous 139612450 14 103270762 103270763 A C 19 GENIC homozygous 139612451 14 103271338 103271339 T G 18 GENIC homozygous 139612452 14 103272332 103272333 G C 28 GENIC homozygous 139612453 14 103273258 103273259 A G 7 GENIC homozygous 139612454 14 103273339 103273340 A 9 GENIC homozygous 139414621 14 103276368 103276369 A C 10 GENIC homozygous 139612459 14 103273820 103273821 A C 13 GENIC homozygous 139612455 14 103273867 103273868 C T 11 GENIC homozygous 139612456 14 103274876 103274877 G A 14 GENIC homozygous 139612457 14 103274913 103274914 A C 16 GENIC homozygous 139612458 14 103277170 103277170 TTTTAA 14 GENIC homozygous 139414622 14 103277171 103277171 ATT 15 GENIC homozygous 139414623 14 103277173 103277175 GC 14 GENIC homozygous 139414624 14 103277177 103277177 TAATTTATA 13 GENIC homozygous 139414625 14 103282611 103282611 A 7 GENIC homozygous 139414626 14 103283947 103283948 C T 18 GENIC homozygous 139612463 14 103277728 103277729 C T 13 GENIC homozygous 139612460 14 103278357 103278358 T C 21 GENIC homozygous 139612461 14 103282834 103282835 A G 17 GENIC homozygous 139612462 14 103284190 103284191 C T 16 GENIC homozygous 139612464 14 103284252 103284253 C T 16 GENIC homozygous 139612465 14 103284477 103284478 A G 13 GENIC homozygous 139612466 14 103285725 103285726 A 16 GENIC homozygous 139414627