chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 34614930 34614931 C T 20 GENIC homozygous 630742511 4 34617082 34617083 T C 26 GENIC possibly homozygous 630742512 4 34617819 34617820 T C 19 GENIC possibly homozygous 630742513 4 34618038 34618039 T C 16 GENIC homozygous 630742514 4 34619139 34619140 G A 25 GENIC possibly homozygous 630742515 4 34619476 34619477 G T 21 GENIC possibly homozygous 630742516 4 34620301 34620302 A G 20 GENIC homozygous 630742517 4 34620321 34620322 C T 19 GENIC possibly homozygous 630742518 4 34620481 34620482 C T 6 GENIC heterozygous 630742519 4 34620704 34620705 G A 8 GENIC possibly homozygous 630742520 4 34620709 34620710 C A 7 GENIC possibly homozygous 630742521 4 34620737 34620738 C T 24 GENIC possibly homozygous 630742522 4 34621147 34621148 A G 16 GENIC homozygous 630742523 4 34621152 34621155 AAA --- 14 GENIC homozygous 745433496 4 34621314 34621315 G T 17 GENIC possibly homozygous 630742524 4 34621519 34621520 G GA 3 GENIC heterozygous 745433497 4 34621896 34621897 T C 5 GENIC heterozygous 630742525 4 34622438 34622439 C T 26 GENIC homozygous 630742526 4 34622718 34622719 T TTG 12 GENIC heterozygous 745433499 4 34622768 34622769 G A 16 GENIC possibly homozygous 630742527 4 34622915 34622916 T C 10 GENIC possibly homozygous 630742528 4 34623082 34623083 A - 5 GENIC homozygous 745433500 4 34623090 34623091 G A 7 GENIC homozygous 630742529 4 34623565 34623566 A G 24 GENIC possibly homozygous 630742530 4 34624035 34624036 G A 15 GENIC possibly homozygous 630742531 4 34624232 34624233 T C 21 GENIC homozygous 630742532