chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 40497460 40497461 T C 28 GENIC homozygous 988724178 10 40497597 40497598 G A 33 GENIC homozygous 988724179 10 40497663 40497664 A C 22 GENIC homozygous 988724180 10 40497696 40497697 G A 21 GENIC homozygous 988724181 10 40497799 40497800 G A 30 GENIC homozygous 988724182 10 40497808 40497809 G A 28 GENIC homozygous 988724183 10 40500253 40500254 C T 30 GENIC homozygous 988724184 10 40500411 40500412 A G 24 GENIC homozygous 988724185 10 40500473 40500474 G T 18 GENIC homozygous 988724186 10 40500850 40500851 G A 38 GENIC homozygous 988724187 10 40502087 40502088 C T 40 GENIC homozygous 988724188 10 40502880 40502881 A G 34 GENIC homozygous 988724189 10 40503320 40503321 T C 28 GENIC homozygous 988724190 10 40503555 40503556 C T 22 GENIC homozygous 988724191 10 40503628 40503629 T A 30 GENIC homozygous 988724192 10 40504813 40504814 C G 21 GENIC homozygous 988724193 10 40505905 40505906 A G 27 GENIC homozygous 988724194 10 40507861 40507862 T C 19 GENIC homozygous 988724195 10 40508000 40508001 T C 33 GENIC homozygous 988724196 10 40513888 40513889 T C 36 GENIC homozygous 988724197 10 40514670 40514671 C T 35 GENIC homozygous 988724198 10 40514804 40514805 T C 47 GENIC homozygous 988724199 10 40516162 40516163 A C 40 GENIC homozygous 988724200 10 40516977 40516978 T C 25 GENIC homozygous 988724201 10 40517613 40517614 A G 26 GENIC homozygous 988724202 10 40517786 40517787 C T 17 GENIC homozygous 988724203 10 40518324 40518325 C A 12 GENIC homozygous 988724204 10 40518670 40518671 A G 29 GENIC homozygous 988724205 10 40519077 40519078 A C 32 GENIC homozygous 988724206 10 40519700 40519701 G A 50 GENIC homozygous 988724207 10 40522778 40522779 T C 18 GENIC homozygous 988724208 10 40523852 40523853 C T 11 GENIC homozygous 988724209