chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 97227996 97227997 A C 53 GENIC homozygous 137559206 5 97228112 97228113 T C 61 GENIC homozygous 137559207 5 97228321 97228322 A G 56 GENIC homozygous 137559208 5 97229171 97229172 T C 55 GENIC homozygous 137559209 5 97229652 97229653 C T 54 GENIC homozygous 137559210 5 97229804 97229805 T C 53 GENIC homozygous 137559211 5 97229938 97229939 C T 51 GENIC homozygous 137559212 5 97230202 97230203 G A 58 GENIC homozygous 137559213 5 97233693 97233694 T A 49 GENIC homozygous 137559214 5 97233727 97233728 G T 50 GENIC homozygous 137559215 5 97233840 97233841 C T 52 GENIC homozygous 137559216 5 97235067 97235068 A T 66 GENIC homozygous 137559217 5 97236377 97236378 G T 68 GENIC homozygous 137559218 5 97237272 97237273 C T 62 GENIC homozygous 137559219 5 97239833 97239834 C G 66 GENIC homozygous 137559220 5 97240212 97240213 C T 52 GENIC homozygous 137559221 5 97242917 97242918 A G 49 GENIC homozygous 137559222 5 97245580 97245581 G A 55 GENIC homozygous 137559223 5 97245589 97245590 A G 56 GENIC homozygous 137559224 5 97249558 97249559 C T 63 GENIC homozygous 137559225 5 97233698 97233698 C 49 GENIC homozygous 137327459 5 97235201 97235203 AT 61 GENIC homozygous 137327460 5 97255209 97255210 T C 68 GENIC homozygous 137559226 5 97256146 97256147 A T 66 GENIC homozygous 137559227 5 97267318 97267319 G T 45 GENIC possibly homozygous 137559228 5 97271273 97271274 A 52 GENIC homozygous 137327461 5 97272997 97272997 AATC 40 GENIC homozygous 137327462 5 97274350 97274350 A 53 GENIC possibly homozygous 137327463 5 97275266 97275267 A G 40 GENIC homozygous 137559229 5 97286832 97286833 G A 65 GENIC homozygous 137559230