chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 37564004 37564005 C A 24 GENIC homozygous 939036296 12 37564549 37564550 T C 22 GENIC homozygous 939036297 12 37564784 37564785 T C 14 GENIC homozygous 939036298 12 37566834 37566835 A G 13 GENIC homozygous 939036299 12 37567045 37567046 T C 15 GENIC homozygous 939036300 12 37567276 37567277 A C 25 GENIC homozygous 939036301 12 37567281 37567282 C A 26 GENIC homozygous 939036302 12 37567397 37567398 T C 23 GENIC homozygous 939036303 12 37567898 37567899 C T 16 GENIC homozygous 939036304 12 37567939 37567940 A C 14 GENIC homozygous 939036305 12 37569481 37569482 C G 18 GENIC homozygous 939036306 12 37569732 37569733 G A 20 GENIC homozygous 939036307 12 37570869 37570870 G A 18 GENIC homozygous 939036308 12 37571673 37571674 A G 21 GENIC homozygous 939036309 12 37572327 37572328 G A 27 GENIC homozygous 939036310 12 37576292 37576293 G A 15 GENIC homozygous 939036311 12 37578715 37578716 C A 20 GENIC homozygous 939036312 12 37579482 37579483 T C 21 GENIC homozygous 939036313 12 37579916 37579917 G T 19 GENIC homozygous 939036314 12 37579917 37579918 A G 18 GENIC homozygous 939036315 12 37579958 37579959 C T 22 GENIC homozygous 939036316