chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 36329357 36329357 A 19 GENIC homozygous 129530315 18 36331117 36331123 CTCTCA 22 GENIC possibly homozygous 135232471 18 36331132 36331132 G 26 GENIC possibly homozygous 135232472 18 36331138 36331147 TCTCTCTCT 26 GENIC homozygous 135056576 18 36331147 36331148 C A 26 GENIC homozygous 135057284 18 36331150 36331165 GCGCGCCTGCGCGGG 27 GENIC homozygous 135056577 18 36331171 36331172 T A 30 GENIC homozygous 131548135 18 36331180 36331181 A T 33 GENIC homozygous 131548136 18 36331182 36331183 A T 35 GENIC homozygous 131548137 18 36331185 36331186 T G 35 GENIC homozygous 131548138 18 36331191 36331192 A T 36 GENIC homozygous 131548139 18 36331194 36331194 CAGTCCTAGC 38 GENIC homozygous 131542562 18 36331197 36331198 A 41 GENIC homozygous 131542563 18 36331203 36331203 CCC 41 GENIC homozygous 131542564 18 36331205 36331205 CATCTATTTCATCATAATGTCTATAT 44 GENIC homozygous 131542565 18 36331206 36331207 G A 49 GENIC homozygous 131548140 18 36331209 36331209 T 49 GENIC homozygous 131542566 18 36331210 36331211 G C 50 GENIC homozygous 131548141 18 36331212 36331213 G C 50 GENIC homozygous 131548142