chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 53092121 53092122 G A 24 GENIC homozygous 47430701 17 53093095 53093096 T G 28 GENIC homozygous 47132483 17 53093150 53093151 T G 28 GENIC homozygous 47132484 17 53093152 53093153 A G 28 GENIC homozygous 47132485 17 53093765 53093766 T C 18 GENIC homozygous 47132490 17 53093208 53093209 G C 31 GENIC homozygous 47132486 17 53093515 53093517 GT -- 19 GENIC homozygous 47132487 17 53093629 53093630 T TA 28 GENIC homozygous 47132488 17 53093663 53093664 C T 27 GENIC homozygous 47132489 17 53093901 53093902 A G 16 GENIC homozygous 47132491 17 53094404 53094405 A T 20 GENIC homozygous 47132492 17 53094453 53094454 A G 10 GENIC homozygous 47132493 17 53094456 53094457 G A 10 GENIC homozygous 47132494 17 53094690 53094691 C CA 20 GENIC homozygous 47132495 17 53095395 53095396 A AT 21 GENIC homozygous 47132498 17 53099289 53099290 G C 16 GENIC homozygous 47327808 17 53099582 53099583 T A 23 GENIC homozygous 47132506 17 53099611 53099614 GGG --- 15 GENIC homozygous 47132507 17 53099626 53099627 A G 18 GENIC homozygous 47709925 17 53099658 53099659 G A 19 GENIC homozygous 47430707 17 53099754 53099774 ATGTAAGTCCTTAGTTCTAC -------------------- 32 GENIC homozygous 47327810 17 53100569 53100570 T TGAGAGA 2 GENIC heterozygous 47742832 17 53101084 53101085 G A 19 GENIC homozygous 47327812 17 53101143 53101144 A C 24 GENIC homozygous 47327814 17 53101153 53101154 A C 25 GENIC homozygous 47327816 17 53101308 53101309 G A 26 GENIC homozygous 47132516 17 53101318 53101319 C T 30 GENIC homozygous 47327818 17 53101373 53101374 C G 29 GENIC homozygous 47327820 17 53101391 53101392 G A 27 GENIC homozygous 47327822 17 53102071 53102072 G T 22 GENIC homozygous 47327824 17 53102236 53102237 A ATGTGTGCGTG 13 GENIC homozygous 47809728 17 53102282 53102283 G GCGTGTGTGT 12 GENIC homozygous 47809730 17 53102295 53102296 C CGTGT 13 GENIC homozygous 47742838 17 53102301 53102302 C CATGTGTGTGTGCATATGTGTGTGCATGTGTGT 3 GENIC homozygous 47809732