chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 36088158 36088159 A G 26 GENIC homozygous 115825418 11 36088194 36088195 A C 26 GENIC homozygous 115825420 11 36088296 36088297 T 17 GENIC possibly homozygous 128899632 11 36088487 36088488 A T 20 GENIC homozygous 115825422 11 36088523 36088524 C T 20 GENIC homozygous 115825424 11 36088537 36088538 A G 20 GENIC homozygous 115825426 11 36088565 36088566 T G 19 GENIC homozygous 115825428 11 36088961 36088962 T C 23 GENIC homozygous 115825430 11 36088991 36088992 A T 25 GENIC homozygous 115825432 11 36089614 36089615 A G 20 GENIC homozygous 115825434 11 36089901 36089902 A G 22 GENIC homozygous 115825436 11 36090068 36090069 G A 35 GENIC homozygous 115825439 11 36090248 36090249 G A 28 GENIC homozygous 115825441 11 36090250 36090251 T C 28 GENIC homozygous 115825443 11 36090924 36090925 T G 24 GENIC homozygous 115825445 11 36090926 36090927 G A 25 GENIC homozygous 115825447 11 36091246 36091249 TGT 18 GENIC homozygous 128899633 11 36091313 36091313 T 18 GENIC homozygous 128899634 11 36091370 36091371 T C 18 GENIC homozygous 115825449 11 36091504 36091505 G A 18 GENIC homozygous 115825451 11 36091855 36091856 C T 15 GENIC homozygous 115825453 11 36092158 36092159 C T 21 GENIC homozygous 115825455 11 36091128 36091129 T A 18 GENIC homozygous 116038359 11 36092296 36092297 A T 28 GENIC homozygous 118143691 11 36092303 36092304 A G 27 GENIC homozygous 118143693 11 36091122 36091123 T C 18 GENIC homozygous 115962295