chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 107371510 107371511 C T 46 GENIC homozygous 72445054 3 107372857 107372858 T C 22 GENIC homozygous 72074338 3 107374964 107374965 T C 25 GENIC homozygous 72074344 3 107381199 107381200 C T 4 GENIC homozygous 72074352 3 107381348 107381349 T G 5 GENIC homozygous 72074354 3 107382270 107382271 T C 12 GENIC homozygous 72074362 3 107382345 107382346 G T 8 GENIC homozygous 72074364 3 107382432 107382433 T G 19 GENIC homozygous 72074368 3 107382489 107382490 G T 15 GENIC homozygous 72074370 3 107382532 107382533 T C 17 GENIC homozygous 72074374 3 107384188 107384189 T C 22 INTERGENIC homozygous 72074386 3 107391156 107391157 G A 5 INTERGENIC heterozygous 72445064 3 107398010 107398011 C A 43 INTERGENIC possibly homozygous 72445067 3 107392316 107392317 A G 11 INTERGENIC heterozygous 73240799 3 107402129 107402130 A G 36 GENIC homozygous 72074442 3 107405853 107405854 A C 34 GENIC homozygous 72445082 3 107411181 107411182 G A 7 GENIC homozygous 72074462 3 107412950 107412951 T A 6 GENIC homozygous 72445086 3 107415216 107415217 C G 5 GENIC homozygous 72445089 3 107415483 107415484 A G 27 GENIC homozygous 72074478 3 107416304 107416305 A T 20 GENIC homozygous 72445092 3 107416315 107416316 A G 20 GENIC homozygous 72445095