chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 29447287 29447288 T C 71 GENIC homozygous 109159801 20 29450098 29450099 A G 46 GENIC homozygous 109159809 20 29450564 29450565 A G 27 GENIC homozygous 109159811 20 29451484 29451485 C T 54 GENIC homozygous 109250710 20 29452732 29452733 G C 40 GENIC homozygous 109250712 20 29453273 29453274 T C 56 GENIC homozygous 109159817 20 29453525 29453526 C T 46 GENIC homozygous 109159819 20 29453787 29453788 G A 53 GENIC homozygous 109159821 20 29454418 29454419 C T 25 GENIC homozygous 109159823 20 29455522 29455523 C T 77 GENIC homozygous 109159825 20 29455528 29455529 G A 75 GENIC homozygous 109250714 20 29455809 29455810 C T 34 GENIC homozygous 109250716 20 29456392 29456393 G C 31 GENIC homozygous 109159827 20 29457259 29457260 G A 29 GENIC homozygous 109250718 20 29457774 29457775 G A 49 GENIC homozygous 109250720 20 29461638 29461639 A G 33 GENIC possibly homozygous 109159831 20 29462774 29462775 C T 45 GENIC homozygous 109310547 20 29462837 29462838 C T 66 GENIC homozygous 109250724 20 29463413 29463414 G A 5 GENIC homozygous 109159835