chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 33572846 33572847 G A 15 GENIC homozygous 973753273 14 33573049 33573050 G A 14 GENIC homozygous 973753274 14 33573318 33573319 T G 20 GENIC homozygous 973753275 14 33573789 33573790 C T 18 GENIC homozygous 973753276 14 33573812 33573813 A G 15 GENIC homozygous 973753277 14 33574099 33574100 A G 15 GENIC homozygous 973753278 14 33574359 33574360 A G 20 GENIC homozygous 973753279 14 33574511 33574512 T C 21 GENIC homozygous 973753280 14 33574924 33574925 C T 20 GENIC homozygous 973753281 14 33575938 33575939 T C 26 GENIC homozygous 973753282 14 33576070 33576071 A G 15 GENIC homozygous 973753283 14 33576171 33576172 C G 17 GENIC homozygous 973753284 14 33577072 33577073 G A 20 GENIC homozygous 973753285 14 33578885 33578886 C G 14 GENIC homozygous 973753286 14 33579113 33579114 A G 20 GENIC homozygous 973753287 14 33579511 33579512 C T 22 GENIC homozygous 973753288 14 33579543 33579544 C A 19 GENIC homozygous 973753289 14 33580028 33580029 A G 24 GENIC homozygous 973753290 14 33580207 33580208 T A 31 GENIC homozygous 973753291 14 33580214 33580215 A G 33 GENIC homozygous 973753292