chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 61233048 61233049 G C 37 GENIC homozygous 526732753 7 61233195 61233196 G T 34 GENIC homozygous 526732754 7 61233319 61233320 C G 18 GENIC heterozygous 526732755 7 61233321 61233322 C A 15 GENIC heterozygous 526732756 7 61233325 61233326 T G 9 GENIC homozygous 526732757 7 61233339 61233340 C G 19 GENIC heterozygous 526732758 7 61233341 61233342 T A 15 GENIC homozygous 526732759 7 61233345 61233346 C G 23 GENIC possibly homozygous 526732760 7 61233365 61233366 G GTC 19 GENIC homozygous 692527637 7 61233416 61233422 TCTCTC ------ 11 GENIC heterozygous 692527638 7 61233418 61233422 TCTC ---- 11 GENIC possibly homozygous 692527639 7 61233543 61233544 T C 38 GENIC homozygous 526732761 7 61233888 61233889 A T 37 GENIC homozygous 526732762 7 61233986 61233987 T C 57 GENIC homozygous 526732763 7 61234081 61234082 C G 38 GENIC homozygous 526732764 7 61234400 61234401 A T 30 GENIC homozygous 526732765 7 61234437 61234438 C T 33 GENIC homozygous 526732766 7 61234780 61234781 C T 17 GENIC homozygous 526732767 7 61235177 61235178 A G 25 GENIC homozygous 526732768 7 61235431 61235432 T G 33 GENIC homozygous 526732769 7 61236018 61236019 C T 30 GENIC homozygous 526732770 7 61236082 61236083 A C 20 GENIC homozygous 526732771 7 61236189 61236190 T C 31 GENIC homozygous 526732772 7 61236368 61236369 C T 27 GENIC homozygous 526732773 7 61236469 61236470 A G 26 GENIC homozygous 526732774 7 61236567 61236568 G A 15 GENIC homozygous 526732775