chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 103918766 103918767 G T 28 GENIC heterozygous 925261439 6 103918907 103918908 C G 32 GENIC heterozygous 925261440 6 103918928 103918929 G A 34 GENIC heterozygous 925261441 6 103919000 103919001 C T 35 GENIC heterozygous 925261442 6 103919126 103919127 T C 49 GENIC heterozygous 925261443 6 103923827 103923828 C T 26 GENIC heterozygous 925261444 6 103923998 103923999 C G 20 GENIC heterozygous 925261445 6 103925867 103925868 T TGTACGA 31 GENIC heterozygous 925312902 6 103928455 103928459 CTCG ---- 19 GENIC heterozygous 925312903 6 103929380 103929381 A AAG 19 GENIC heterozygous 925312904 6 103929383 103929384 G A 17 GENIC heterozygous 925261446 6 103929500 103929504 TTTT ---- 22 GENIC heterozygous 925312905 6 103929966 103929967 C T 34 GENIC heterozygous 925261447 6 103930792 103930793 T C 43 GENIC heterozygous 925261448 6 103931273 103931274 G A 29 GENIC heterozygous 925261449 6 103935282 103935283 T C 34 GENIC heterozygous 925261450