chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 58516136 58516137 A C 4 GENIC homozygous 532458511 6 58516274 58516275 C T 32 GENIC heterozygous 532458512 6 58516311 58516312 A C 37 GENIC heterozygous 532458513 6 58516889 58516890 T TC 9 GENIC homozygous 694050904 6 58517369 58517370 T TG 16 GENIC homozygous 694050905 6 58518264 58518265 T - 10 GENIC homozygous 694050906 6 58518573 58518574 T TAA 7 GENIC homozygous 694050907 6 58518588 58518589 C - 15 GENIC homozygous 694050908 6 58518869 58518870 A T 9 GENIC homozygous 529578512 6 58519015 58519016 C T 16 GENIC homozygous 532458514 6 58519962 58519963 C T 16 GENIC homozygous 529578513 6 58520149 58520165 TCTCTCTCTCTCTCTC ---------------- 4 GENIC homozygous 694050909 6 58520204 58520205 C G 12 GENIC heterozygous 532458515 6 58520228 58520229 T G 13 GENIC heterozygous 532458516 6 58521859 58521860 C CA 4 GENIC homozygous 694050910 6 58522320 58522321 C G 31 GENIC homozygous 529578514 6 58523522 58523523 C T 31 GENIC homozygous 529578515 6 58524266 58524267 T TTCAA 13 GENIC homozygous 694050911 6 58524268 58524269 G GC 8 GENIC homozygous 694050912 6 58524269 58524270 T TTCA 9 GENIC homozygous 694050913 6 58525043 58525044 G T 26 GENIC possibly homozygous 529578516 6 58525046 58525047 G A 26 GENIC possibly homozygous 529578517 6 58526277 58526278 T A 15 GENIC heterozygous 532458517 6 58526279 58526280 T A 15 GENIC heterozygous 532458518 6 58526281 58526282 T A 15 GENIC heterozygous 532458519 6 58526969 58526970 T C 17 GENIC homozygous 529578518 6 58527200 58527201 C T 10 GENIC homozygous 529578519 6 58528608 58528609 T TAAA 13 GENIC homozygous 694050915 6 58528754 58528755 G GA 25 GENIC homozygous 694050916