chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 81850423 81850424 T C 19 GENIC homozygous 113501580 14 81856307 81856308 G A 25 GENIC homozygous 113603661 14 81859704 81859705 C G 19 GENIC homozygous 113603662 14 81862567 81862568 A G 38 GENIC homozygous 113603663 14 81869131 81869132 C T 22 GENIC homozygous 113603664 14 81872224 81872225 G T 26 GENIC homozygous 113603665 14 81878183 81878184 T C 31 GENIC homozygous 113603666 14 81878377 81878378 T G 25 GENIC homozygous 113603667 14 81933372 81933373 T C 28 GENIC homozygous 113603668 14 81938975 81938976 T C 15 GENIC homozygous 113603669 14 81952623 81952624 G A 28 GENIC homozygous 113603671 14 81963279 81963280 T C 19 GENIC homozygous 113603672 14 81968179 81968180 C T 15 GENIC homozygous 113603673 14 81983038 81983039 G A 30 GENIC homozygous 113603674 14 81990530 81990531 A T 31 GENIC homozygous 113603675 14 81992962 81992963 A G 30 GENIC homozygous 113603676 14 82002859 82002860 C G 19 GENIC homozygous 113603677 14 82003797 82003798 G A 23 GENIC homozygous 113603679 14 82004618 82004619 C T 20 GENIC homozygous 113603680 14 82004842 82004843 G A 20 GENIC homozygous 113603681 14 82005003 82005004 G A 22 GENIC homozygous 113603682 14 82005035 82005036 C T 26 GENIC homozygous 113603683 14 82005189 82005190 A G 31 GENIC homozygous 113603684 14 82009984 82009985 A G 17 GENIC homozygous 113603685 14 82009985 82009986 G A 17 GENIC homozygous 113603686 14 82010277 82010278 T C 22 GENIC homozygous 113603687 14 82013105 82013106 A C 17 GENIC homozygous 113603688 14 82016464 82016465 G A 20 GENIC homozygous 113603689 14 82018038 82018039 C T 28 GENIC homozygous 113603690 14 82029608 82029609 A G 23 GENIC homozygous 113603691 14 81922131 81922132 C G 2 GENIC homozygous 113679749 14 81922147 81922148 C G 2 GENIC homozygous 113679751 14 81968540 81968541 T G 21 GENIC possibly homozygous 113679753 14 82009493 82009494 T A 30 GENIC homozygous 113679755