chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 47552943 47552944 G C 25 GENIC homozygous 115344309 12 47553145 47553146 A G 18 GENIC homozygous 115344311 12 47553191 47553192 C T 21 GENIC homozygous 115344313 12 47553421 47553422 A G 23 GENIC homozygous 115344315 12 47553578 47553579 C T 22 GENIC homozygous 115344317 12 47553600 47553601 T C 24 GENIC homozygous 115344319 12 47553668 47553669 G A 16 GENIC homozygous 115344321 12 47554267 47554268 G T 19 GENIC homozygous 115397638 12 47554299 47554300 G C 12 GENIC homozygous 115397640 12 47554556 47554557 A T 16 GENIC homozygous 115344323 12 47554612 47554613 C A 18 GENIC homozygous 115344325 12 47554613 47554614 A G 18 GENIC homozygous 115344327 12 47554918 47554919 C T 14 GENIC homozygous 115344329 12 47554929 47554930 A G 13 GENIC homozygous 115344331 12 47555122 47555123 T C 24 GENIC homozygous 115344333 12 47555183 47555184 C A 18 GENIC homozygous 115344335 12 47555556 47555557 G A 19 GENIC homozygous 115344337 12 47555660 47555661 G T 19 GENIC homozygous 115397646 12 47556222 47556223 C T 28 GENIC homozygous 115344339 12 47556348 47556349 A G 24 GENIC homozygous 115344341