chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 66341936 66341937 C A 20 GENIC homozygous 51479540 10 66343029 66343030 C T 22 GENIC homozygous 51479541 10 66350666 66350667 A G 14 GENIC homozygous 51479543 10 66350764 66350765 A ATTTTTT 3 GENIC homozygous 51907945 10 66351483 66351484 C T 20 GENIC homozygous 51479547 10 66351527 66351528 G A 20 GENIC homozygous 51907947 10 66352061 66352062 T A 20 GENIC possibly homozygous 51479548 10 66352225 66352226 G A 15 GENIC homozygous 51479549 10 66352692 66352693 T - 7 GENIC homozygous 51907949 10 66352940 66352942 CT -- 5 GENIC homozygous 51479551 10 66352952 66352953 G - 4 GENIC homozygous 51479552 10 66353719 66353720 C T 16 GENIC homozygous 51479554 10 66354076 66354077 G - 17 GENIC homozygous 51907951 10 66354336 66354337 G A 23 GENIC homozygous 51479561 10 66354736 66354737 A G 27 GENIC possibly homozygous 51479562 10 66354841 66354856 TGCCCTCTTCTGGTG --------------- 7 GENIC heterozygous 51479563 10 66354913 66354915 CC -- 9 GENIC homozygous 51479564 10 66354929 66354930 C - 12 GENIC possibly homozygous 51479565 10 66354930 66354931 C A 11 GENIC possibly homozygous 51907953 10 66355017 66355018 A - 22 GENIC homozygous 51479566 10 66355169 66355170 C CAAAA 1 GENIC homozygous 51479567 10 66355372 66355373 T TA 10 GENIC homozygous 51479568 10 66355389 66355390 A - 6 GENIC homozygous 51907955 10 66355414 66355415 G T 9 GENIC possibly homozygous 51479569 10 66355439 66355440 C CAA 4 GENIC homozygous 51479570 10 66355454 66355455 C A 13 GENIC homozygous 51678708