chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 30161084 30161085 A G 32 GENIC homozygous 970609425 12 30165458 30165459 G T 39 GENIC homozygous 970609426 12 30166404 30166405 C T 27 GENIC homozygous 970609427 12 30166464 30166465 C A 47 GENIC homozygous 970609428 12 30166939 30166940 T A 26 GENIC homozygous 970609429 12 30166941 30166942 A C 25 GENIC homozygous 970609430 12 30167445 30167446 A G 28 GENIC homozygous 970609431 12 30168373 30168374 G A 24 GENIC homozygous 970609432 12 30170287 30170288 A G 35 GENIC homozygous 970609433 12 30171217 30171218 T C 35 GENIC homozygous 970609434 12 30172688 30172689 T G 26 GENIC homozygous 970609435 12 30172829 30172830 A C 29 GENIC homozygous 970609436 12 30176130 30176131 G A 28 GENIC homozygous 970609437 12 30176322 30176323 T G 30 GENIC homozygous 970609438 12 30177010 30177011 T C 38 GENIC homozygous 970609439 12 30177099 30177100 T C 32 GENIC homozygous 970609440 12 30177201 30177202 T C 35 GENIC homozygous 970609441 12 30177264 30177265 A G 36 GENIC homozygous 970609442 12 30177318 30177319 G A 38 GENIC homozygous 970609443 12 30177583 30177584 T C 31 GENIC homozygous 970609444