chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 41801055 41801056 G A 23 GENIC homozygous 983692233 17 41801228 41801229 T C 24 GENIC homozygous 983692234 17 41801899 41801900 G A 20 GENIC homozygous 983692235 17 41802420 41802421 G A 26 GENIC homozygous 983692236 17 41802895 41802896 T C 27 GENIC homozygous 983692237 17 41803064 41803065 G A 28 GENIC homozygous 983692238 17 41803331 41803332 A G 26 GENIC homozygous 983692239 17 41803723 41803724 A G 26 GENIC homozygous 983692240 17 41803867 41803868 C A 18 GENIC heterozygous 983692241 17 41804579 41804580 C A 24 GENIC homozygous 983692242 17 41804691 41804692 A T 40 GENIC homozygous 983692243 17 41805049 41805050 A G 22 GENIC homozygous 983692244 17 41805653 41805654 G A 11 GENIC homozygous 983692245 17 41805760 41805761 T C 8 GENIC homozygous 983692246 17 41807132 41807133 C T 24 GENIC homozygous 983692247 17 41807849 41807850 T C 28 GENIC homozygous 983692248 17 41808996 41808997 A G 23 GENIC homozygous 983692249 17 41809399 41809400 C G 8 GENIC homozygous 983692250 17 41809606 41809607 C T 11 GENIC homozygous 983692251 17 41809607 41809608 T A 11 GENIC homozygous 983692252 17 41811273 41811274 T C 17 GENIC homozygous 983692253 17 41811480 41811481 G A 19 GENIC homozygous 983692254 17 41811519 41811520 T G 15 GENIC homozygous 983692255 17 41811800 41811801 T C 19 GENIC homozygous 983692256 17 41815395 41815396 G A 18 GENIC homozygous 983692257