chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 58516136 58516137 A C 7 GENIC homozygous 505969592 6 58516274 58516275 C T 63 GENIC heterozygous 505969593 6 58516311 58516312 A C 83 GENIC heterozygous 505969594 6 58516889 58516890 T TC 8 GENIC homozygous 684033551 6 58517369 58517370 T TG 22 GENIC homozygous 684033552 6 58518264 58518265 T - 28 GENIC homozygous 684033553 6 58518573 58518574 T TAA 8 GENIC homozygous 684033554 6 58518588 58518589 C - 17 GENIC homozygous 684033555 6 58518869 58518870 A T 45 GENIC homozygous 502805748 6 58519962 58519963 C T 21 GENIC homozygous 502805749 6 58520149 58520165 TCTCTCTCTCTCTCTC ---------------- 3 GENIC heterozygous 684033556 6 58520204 58520205 C G 18 GENIC heterozygous 505969595 6 58520228 58520229 T G 23 GENIC heterozygous 505969596 6 58521859 58521860 C CA 12 GENIC homozygous 684033557 6 58522320 58522321 C G 56 GENIC homozygous 502805750 6 58523522 58523523 C T 57 GENIC homozygous 502805751 6 58524266 58524267 T TTCAA 19 GENIC homozygous 684033558 6 58524268 58524269 G GC 14 GENIC homozygous 684033559 6 58524269 58524270 T TTCA 14 GENIC homozygous 684033560 6 58525043 58525044 G T 30 GENIC possibly homozygous 502805752 6 58525046 58525047 G A 29 GENIC homozygous 502805753 6 58526279 58526280 T A 49 GENIC heterozygous 505969597 6 58526281 58526282 T A 50 GENIC possibly homozygous 505969598 6 58526969 58526970 T C 19 GENIC homozygous 502805754 6 58527200 58527201 C T 27 GENIC homozygous 502805755 6 58528608 58528609 T TAAA 30 GENIC homozygous 684033562 6 58528754 58528755 G GA 19 GENIC homozygous 684033563