chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 43548625 43548626 T C 32 GENIC homozygous 541345104 8 43548762 43548763 T C 16 GENIC homozygous 541345105 8 43548955 43548956 C T 28 GENIC homozygous 541345106 8 43549569 43549570 A G 40 GENIC homozygous 539126778 8 43549609 43549610 C T 38 GENIC homozygous 539126779 8 43550054 43550055 T C 17 GENIC homozygous 541345107 8 43550063 43550070 GACTCGG ------- 12 GENIC homozygous 697516497 8 43550301 43550302 T C 29 GENIC homozygous 541345108 8 43550382 43550383 C T 11 GENIC homozygous 541345109 8 43550408 43550413 AAGAG ----- 6 GENIC heterozygous 697516498 8 43550410 43550413 GAG --- 5 GENIC homozygous 697516499 8 43550412 43550413 G - 5 GENIC homozygous 697516500 8 43550486 43550489 CTT --- 16 GENIC homozygous 697516501 8 43550656 43550657 A AG 30 GENIC homozygous 697516502 8 43550890 43550891 G A 18 GENIC homozygous 539126780 8 43551051 43551052 T TG 24 GENIC homozygous 697516503 8 43551298 43551299 C T 40 GENIC homozygous 541345110 8 43551392 43551393 C CT 17 GENIC possibly homozygous 697516504 8 43551778 43551779 A AT 3 GENIC homozygous 697516505 8 43552039 43552040 C T 45 GENIC homozygous 541345111