chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 41801055 41801056 G A 21 GENIC homozygous 959503181 17 41801228 41801229 T C 25 GENIC homozygous 959503182 17 41801899 41801900 G A 25 GENIC possibly homozygous 959503183 17 41802420 41802421 G A 18 GENIC homozygous 959503184 17 41802895 41802896 T C 29 GENIC homozygous 959503185 17 41803064 41803065 G A 25 GENIC homozygous 959503186 17 41803331 41803332 A G 29 GENIC homozygous 959503187 17 41803723 41803724 A G 20 GENIC homozygous 959503188 17 41804579 41804580 C A 25 GENIC homozygous 959503189 17 41804691 41804692 A T 23 GENIC homozygous 959503190 17 41805049 41805050 A G 26 GENIC homozygous 959503191 17 41805653 41805654 G A 20 GENIC homozygous 959503192 17 41805760 41805761 T C 28 GENIC homozygous 959503193 17 41806052 41806053 G T 24 GENIC homozygous 959503194 17 41807132 41807133 C T 31 GENIC homozygous 959503195 17 41807849 41807850 T C 22 GENIC homozygous 959503196 17 41808996 41808997 A G 23 GENIC homozygous 959503197 17 41809399 41809400 C G 11 GENIC homozygous 959503198 17 41809606 41809607 C T 26 GENIC homozygous 959503199 17 41809607 41809608 T A 26 GENIC homozygous 959503200 17 41811273 41811274 T C 20 GENIC homozygous 959503201 17 41811480 41811481 G A 38 GENIC homozygous 959503202 17 41811519 41811520 T G 38 GENIC homozygous 959503203 17 41811800 41811801 T C 34 GENIC homozygous 959503204 17 41815347 41815348 A C 24 GENIC possibly homozygous 959503205 17 41815395 41815396 G A 31 GENIC homozygous 959503206