chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 53093095 53093096 T G 4 GENIC homozygous 47132483 17 53093150 53093151 T G 2 GENIC homozygous 47132484 17 53093152 53093153 A G 2 GENIC homozygous 47132485 17 53093208 53093209 G C 8 GENIC homozygous 47132486 17 53093515 53093517 GT -- 6 GENIC homozygous 47132487 17 53093629 53093630 T TA 11 GENIC homozygous 47132488 17 53093663 53093664 C T 12 GENIC homozygous 47132489 17 53093765 53093766 T C 8 GENIC homozygous 47132490 17 53093901 53093902 A G 4 GENIC homozygous 47132491 17 53094404 53094405 A T 5 GENIC homozygous 47132492 17 53094453 53094454 A G 7 GENIC homozygous 47132493 17 53094456 53094457 G A 5 GENIC homozygous 47132494 17 53094690 53094691 C CA 10 GENIC possibly homozygous 47132495 17 53095314 53095315 A G 7 GENIC homozygous 47132496 17 53095355 53095356 A G 11 GENIC homozygous 47132497 17 53095395 53095396 A AT 9 GENIC homozygous 47132498 17 53095823 53095824 T C 8 GENIC homozygous 47132499 17 53095829 53095830 A - 6 GENIC homozygous 47132500 17 53095910 53095911 G A 11 GENIC homozygous 47132501 17 53096657 53096658 T C 8 GENIC homozygous 47132502 17 53096728 53096729 C T 10 GENIC possibly homozygous 47132503 17 53097055 53097056 G A 8 GENIC homozygous 47132504 17 53097220 53097221 C G 7 GENIC homozygous 47132505 17 53099582 53099583 T A 12 GENIC homozygous 47132506 17 53099611 53099614 GGG --- 10 GENIC homozygous 47132507 17 53099915 53099916 G A 10 GENIC homozygous 47132508 17 53100017 53100018 G A 3 GENIC homozygous 47132509 17 53100248 53100249 T G 12 GENIC homozygous 47132510 17 53100373 53100374 G A 7 GENIC homozygous 47132511 17 53102021 53102022 G A 9 GENIC homozygous 47132517 17 53099626 53099627 A G 12 GENIC homozygous 47709925 17 53100569 53100570 T TGAGAGA 1 GENIC homozygous 47742832 17 53102276 53102277 A ATGTGTGCG 7 GENIC homozygous 47742836 17 53102295 53102296 C CGTGT 7 GENIC homozygous 47742838 17 53102301 53102302 C CATGTGTGTGCGCATGTGTGT 7 GENIC homozygous 47742840