chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 10049313 10049314 C A 13 GENIC homozygous 140052149 17 10050597 10050598 T G 23 GENIC homozygous 140052150 17 10050986 10050987 G T 19 GENIC homozygous 140052151 17 10051075 10051075 CTGCCT 15 GENIC homozygous 140008753 17 10051640 10051641 C T 10 GENIC homozygous 140052152 17 10052140 10052141 A G 38 GENIC homozygous 140052153 17 10052275 10052276 G A 30 GENIC homozygous 140052154 17 10052911 10052915 TGCC 26 GENIC homozygous 140008754 17 10054326 10054327 A G 19 GENIC homozygous 140052155 17 10056298 10056299 A G 17 GENIC homozygous 140052156 17 10056510 10056511 C T 25 GENIC homozygous 140052157 17 10056553 10056554 G A 33 GENIC homozygous 140052158 17 10056587 10056588 C T 30 GENIC homozygous 140052159 17 10056812 10056813 C T 16 GENIC homozygous 140052160 17 10056965 10056966 C A 25 GENIC homozygous 140052161 17 10057471 10057472 G C 27 GENIC homozygous 140052162 17 10057892 10057893 A T 34 GENIC homozygous 140052163 17 10058070 10058071 T A 17 GENIC homozygous 140052164 17 10059682 10059683 T C 27 GENIC homozygous 140052172 17 10058116 10058117 C T 19 GENIC homozygous 140052165 17 10058350 10058351 A G 18 GENIC homozygous 140052166 17 10058440 10058441 A T 25 GENIC homozygous 140052167 17 10058598 10058599 A G 16 GENIC homozygous 140052168 17 10058646 10058647 C A 19 GENIC homozygous 140052169 17 10058676 10058677 T G 19 GENIC homozygous 140052170 17 10059530 10059531 C G 22 GENIC homozygous 140052171 17 10060088 10060089 C T 24 GENIC homozygous 140052173 17 10061002 10061003 T G 17 GENIC homozygous 140052174 17 10061010 10061011 C T 14 GENIC homozygous 140052175 17 10061091 10061091 CCT 6 GENIC heterozygous 145221464 17 10061244 10061245 C T 24 GENIC homozygous 140052176 17 10061396 10061415 CTCACTTTGTAGCCGTGGC 16 GENIC homozygous 140008755 17 10061504 10061505 C A 20 GENIC homozygous 140052177