chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 91453252 91453253 G T 24 GENIC homozygous 944683675 10 91454017 91454018 A G 21 GENIC homozygous 944683676 10 91454279 91454280 T C 25 GENIC homozygous 944683677 10 91454318 91454319 A T 21 GENIC homozygous 944683678 10 91455042 91455043 C G 31 GENIC homozygous 944683679 10 91455145 91455146 C T 31 GENIC homozygous 944683680 10 91455199 91455200 A G 27 GENIC homozygous 944683681 10 91455697 91455698 G A 17 GENIC homozygous 944683682 10 91460893 91460894 C T 37 GENIC homozygous 944683683 10 91467129 91467130 T C 37 GENIC homozygous 944683684 10 91468512 91468513 A G 30 GENIC homozygous 944683685 10 91468899 91468900 A G 32 GENIC homozygous 944683686 10 91469117 91469118 C A 42 GENIC homozygous 944683687 10 91470705 91470706 C T 24 GENIC homozygous 944683688 10 91471236 91471237 C T 27 GENIC homozygous 944683689 10 91471540 91471541 C T 42 GENIC homozygous 944683690 10 91472977 91472978 C T 30 GENIC homozygous 944683691 10 91473354 91473355 T G 40 GENIC homozygous 944683692 10 91475268 91475269 C T 38 GENIC homozygous 944683693 10 91475968 91475969 A T 22 GENIC homozygous 944683694 10 91476529 91476530 C T 23 GENIC homozygous 944683695 10 91483196 91483197 T C 28 GENIC homozygous 944683696 10 91485300 91485301 C T 38 GENIC homozygous 944683697 10 91488988 91488989 T C 20 GENIC homozygous 944683698 10 91490135 91490136 C A 29 GENIC homozygous 944683699 10 91490484 91490485 C G 39 GENIC homozygous 944683700 10 91494420 91494421 C T 26 GENIC homozygous 944683701 10 91494479 91494480 G A 26 GENIC homozygous 944683702 10 91495852 91495853 T C 26 GENIC homozygous 944683703 10 91496260 91496261 A T 36 GENIC homozygous 944683704 10 91497128 91497129 G A 28 GENIC homozygous 944683705 10 91497377 91497378 A T 15 GENIC homozygous 944683706 10 91498093 91498094 T C 42 GENIC homozygous 944683707