chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 13965283 13965284 T C 16 GENIC homozygous 109100412 20 13965934 13965935 A G 22 GENIC homozygous 109100414 20 13966702 13966703 G A 22 GENIC homozygous 109240658 20 13966787 13966788 C T 21 GENIC homozygous 109240659 20 13967688 13967689 C T 20 GENIC homozygous 109240660 20 13968380 13968381 A G 22 GENIC homozygous 109100430 20 13968434 13968435 C T 24 GENIC homozygous 109240661 20 13968446 13968447 C T 27 GENIC homozygous 109240662 20 13969163 13969164 C T 16 GENIC homozygous 109240663 20 13969942 13969943 G A 25 GENIC homozygous 109240664 20 13970457 13970458 G A 38 GENIC homozygous 109240665 20 13970766 13970767 G A 32 GENIC homozygous 109240666 20 13970868 13970869 A G 26 GENIC possibly homozygous 109100440 20 13972258 13972259 C T 25 GENIC possibly homozygous 109240667 20 13972261 13972262 G C 25 GENIC possibly homozygous 109240668 20 13971026 13971027 C T 29 GENIC homozygous 109456423