chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 38786828 38786829 A G 23 GENIC homozygous 115323966 12 38787748 38787749 T C 20 GENIC homozygous 115323968 12 38788586 38788587 T C 23 GENIC homozygous 115323970 12 38788962 38788963 C T 20 GENIC homozygous 115476385 12 38790095 38790096 T C 27 GENIC homozygous 115323974 12 38799151 38799152 G A 23 GENIC homozygous 115323980 12 38799213 38799214 T C 26 GENIC homozygous 115323984 12 38799366 38799367 A G 28 GENIC homozygous 115323986 12 38800714 38800715 A G 38 GENIC homozygous 115323990 12 38801017 38801018 C T 28 GENIC homozygous 115323994 12 38801289 38801290 T A 36 GENIC homozygous 115323996 12 38801535 38801536 C G 27 GENIC homozygous 115476387 12 38801539 38801540 G A 26 GENIC homozygous 115476389 12 38801642 38801643 T A 34 GENIC homozygous 115476391 12 38801756 38801757 G A 27 GENIC homozygous 115476393 12 38801973 38801974 T A 32 GENIC homozygous 115476395 12 38802254 38802255 A T 40 GENIC homozygous 115476397 12 38802655 38802656 G T 30 GENIC homozygous 115476399 12 38803462 38803463 A G 21 GENIC homozygous 115476403 12 38803624 38803625 T C 26 GENIC homozygous 115324004 12 38803685 38803686 C T 27 GENIC homozygous 115476405 12 38804082 38804083 G A 25 GENIC homozygous 115476407 12 38804497 38804498 T G 19 GENIC possibly homozygous 115476409