chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 10543058 10543059 T C 29 GENIC homozygous 998687710 17 10543603 10543604 A G 22 GENIC homozygous 998687711 17 10544071 10544072 G A 17 GENIC homozygous 998687712 17 10544121 10544122 G A 16 GENIC homozygous 998687713 17 10544550 10544551 T C 17 GENIC homozygous 998687714 17 10545547 10545548 G A 28 GENIC homozygous 998687715 17 10545688 10545689 G A 22 GENIC homozygous 998687716 17 10545861 10545862 C T 14 GENIC homozygous 998687717 17 10546148 10546149 C T 20 GENIC homozygous 998687718 17 10546256 10546257 T C 26 GENIC homozygous 998687719 17 10546697 10546698 A G 23 GENIC homozygous 998687720 17 10546749 10546750 G A 28 GENIC homozygous 998687721 17 10546825 10546826 A G 30 GENIC homozygous 998687722 17 10546960 10546961 T C 22 GENIC homozygous 998687723 17 10547249 10547250 A G 27 GENIC possibly homozygous 998687724 17 10547571 10547572 C T 25 GENIC homozygous 998687725 17 10547720 10547721 C T 27 GENIC homozygous 998687726 17 10547856 10547857 A C 26 GENIC homozygous 998687727 17 10548488 10548489 G A 27 GENIC homozygous 998687728 17 10548665 10548666 C T 28 GENIC homozygous 998687729 17 10548721 10548722 C T 24 GENIC homozygous 998687730 17 10548996 10548997 A G 15 GENIC homozygous 998687731 17 10549194 10549195 G A 26 GENIC homozygous 998687732 17 10549728 10549729 G T 14 GENIC homozygous 998687733 17 10551170 10551171 G A 29 GENIC homozygous 998687734 17 10552353 10552354 T C 22 GENIC homozygous 998687735 17 10553201 10553202 C T 18 GENIC homozygous 998687736 17 10554013 10554014 A G 32 GENIC homozygous 998687737