chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 45486548 45486550 TT -- 24 GENIC homozygous 51442629 10 45487880 45487881 T - 11 GENIC heterozygous 51636283 10 45487982 45487983 A T 16 GENIC homozygous 51442630 10 45488537 45488538 G A 24 GENIC homozygous 51442631 10 45488631 45488632 A - 19 GENIC homozygous 51442633 10 45488944 45488945 G A 11 GENIC homozygous 51442634 10 45489573 45489574 T A 16 GENIC homozygous 51442635 10 45489785 45489786 T TCCTCTCTCTC 12 GENIC homozygous 52373011 10 45490539 45490540 T C 33 GENIC homozygous 51442637 10 45490577 45490578 A G 41 GENIC homozygous 51442638 10 45490578 45490579 A C 42 GENIC homozygous 51442639 10 45491053 45491054 T C 34 GENIC homozygous 51442640 10 45491121 45491122 G A 44 GENIC homozygous 51442641 10 45491408 45491409 C T 39 GENIC homozygous 51442642 10 45491414 45491415 A C 41 GENIC homozygous 51442643 10 45492629 45492630 A C 32 GENIC homozygous 51442644 10 45492801 45492802 A G 48 GENIC possibly homozygous 51442645 10 45493694 45493696 TT -- 14 GENIC heterozygous 51442646 10 45493695 45493696 T - 14 GENIC heterozygous 51442647 10 45495375 45495376 G GA 46 GENIC homozygous 52373013 10 45495619 45495620 G GACACACAC 9 GENIC heterozygous 52373015 10 45495619 45495620 G GACACACACAC 9 GENIC heterozygous 52373017 10 45495839 45495840 C G 28 GENIC homozygous 51442649 10 45496921 45496922 T C 19 GENIC homozygous 51442650 10 45497142 45497143 C CTT 13 GENIC homozygous 51442651 10 45497554 45497555 C T 45 GENIC homozygous 51442652 10 45498802 45498803 G A 29 GENIC homozygous 51442653 10 45499413 45499414 G A 18 GENIC homozygous 51442654 10 45499636 45499637 T TGAGA 14 GENIC heterozygous 52373019 10 45499761 45499762 T A 34 GENIC homozygous 51442655 10 45500761 45500762 A G 24 GENIC homozygous 51442656 10 45501325 45501326 T C 31 GENIC homozygous 51442657 10 45501335 45501336 A T 33 GENIC homozygous 51442658 10 45501992 45501993 G A 26 GENIC homozygous 51442659 10 45502840 45502841 C CTGTG 17 GENIC heterozygous 52373021 10 45502932 45502933 C CCT 17 GENIC possibly homozygous 51442660