chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 49330656 49330657 T C 21 GENIC homozygous 958975340 12 49330802 49330803 T C 26 GENIC homozygous 958975341 12 49331002 49331003 G A 23 GENIC homozygous 958975342 12 49331242 49331243 T C 31 GENIC homozygous 958975343 12 49331924 49331925 C T 31 GENIC homozygous 958975344 12 49332445 49332446 C T 18 GENIC homozygous 958975345 12 49333270 49333271 A C 30 GENIC homozygous 958975346 12 49333996 49333997 A G 32 GENIC homozygous 958975347 12 49334432 49334433 C G 22 GENIC homozygous 958975348 12 49334857 49334858 G A 33 GENIC homozygous 958975349 12 49335350 49335351 T G 37 GENIC homozygous 958975350 12 49336496 49336497 G T 24 GENIC homozygous 958975351 12 49336497 49336498 T C 23 GENIC homozygous 958975352 12 49336851 49336852 C T 27 GENIC homozygous 958975353 12 49336852 49336853 A G 28 GENIC homozygous 958975354 12 49337448 49337449 A G 21 GENIC homozygous 958975355 12 49338137 49338138 G T 44 GENIC homozygous 958975356 12 49339394 49339395 G C 16 GENIC homozygous 958975357 12 49339446 49339447 C G 13 GENIC homozygous 958975358 12 49340050 49340051 T C 23 GENIC homozygous 958975359 12 49341000 49341001 T C 12 GENIC homozygous 958975360 12 49341210 49341211 C T 25 GENIC homozygous 958975361 12 49358877 49358878 A G 24 GENIC homozygous 958975362 12 49369810 49369811 G A 26 GENIC homozygous 958975363 12 49370024 49370025 C T 15 GENIC homozygous 958975364 12 49372606 49372607 G A 16 GENIC homozygous 958975365 12 49373017 49373018 A G 16 GENIC homozygous 958975366 12 49376541 49376542 A G 14 GENIC homozygous 958975367 12 49386849 49386850 A G 18 GENIC possibly homozygous 958975368 12 49394909 49394910 G A 19 GENIC homozygous 958975369