chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 89162854 89162855 A G 8 GENIC homozygous 891369302 1 89163997 89163998 G A 12 GENIC homozygous 891369303 1 89164575 89164576 G A 15 GENIC homozygous 891369304 1 89164601 89164602 T C 16 GENIC homozygous 891369305 1 89164719 89164720 T C 13 GENIC homozygous 891369306 1 89165307 89165308 T C 12 GENIC homozygous 891369307 1 89166345 89166346 C T 10 GENIC homozygous 891369308 1 89166413 89166414 T A 4 GENIC heterozygous 891369309 1 89167216 89167217 A T 10 GENIC homozygous 891369310 1 89167609 89167610 C T 25 GENIC homozygous 891369311 1 89168244 89168245 G A 6 GENIC homozygous 891369312 1 89168254 89168255 T C 5 GENIC homozygous 891369313 1 89168264 89168265 G T 4 GENIC homozygous 891369314 1 89168277 89168278 C T 8 GENIC homozygous 891369315 1 89168338 89168339 A G 25 GENIC homozygous 891369316 1 89168380 89168381 A G 17 GENIC homozygous 891369317 1 89168425 89168426 G T 18 GENIC homozygous 891369318 1 89168998 89168999 A G 9 GENIC homozygous 891369319 1 89169205 89169206 A C 24 GENIC homozygous 891369320 1 89169818 89169819 C T 16 GENIC homozygous 891369321 1 89170205 89170206 A G 6 GENIC homozygous 891369322 1 89170902 89170903 A G 15 GENIC homozygous 891369323 1 89171782 89171783 C T 18 GENIC homozygous 891369324 1 89172391 89172392 G A 16 GENIC homozygous 891369325 1 89172836 89172837 G T 7 GENIC heterozygous 891369326 1 89172837 89172838 T G 7 GENIC heterozygous 891369327 1 89173131 89173132 C T 20 GENIC homozygous 891369328 1 89173240 89173241 T A 17 GENIC homozygous 891369329 1 89173796 89173797 A G 15 GENIC homozygous 891369330 1 89174151 89174152 A T 10 GENIC homozygous 891369331 1 89174158 89174159 T C 7 GENIC homozygous 891369332 1 89174176 89174177 C A 13 GENIC homozygous 891369333 1 89174298 89174299 C T 14 GENIC homozygous 891369334 1 89174341 89174342 G A 12 GENIC homozygous 891369335 1 89174390 89174391 T C 7 GENIC homozygous 891369336 1 89174519 89174520 T C 10 GENIC homozygous 891369337 1 89175422 89175423 A T 11 GENIC homozygous 891369338