chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 49330656 49330657 T C 23 GENIC homozygous 964860650 12 49330802 49330803 T C 28 GENIC homozygous 964860651 12 49331002 49331003 G A 27 GENIC homozygous 964860652 12 49331099 49331100 A C 25 GENIC homozygous 964860653 12 49331242 49331243 T C 22 GENIC homozygous 964860654 12 49331924 49331925 C T 29 GENIC homozygous 964860655 12 49332445 49332446 C T 15 GENIC homozygous 964860656 12 49333270 49333271 A C 24 GENIC homozygous 964860657 12 49333996 49333997 A G 23 GENIC homozygous 964860658 12 49334432 49334433 C G 33 GENIC homozygous 964860659 12 49334857 49334858 G A 40 GENIC homozygous 964860660 12 49335350 49335351 T G 31 GENIC homozygous 964860661 12 49336496 49336497 G T 27 GENIC homozygous 964860662 12 49336497 49336498 T C 28 GENIC homozygous 964860663 12 49336851 49336852 C T 24 GENIC homozygous 964860664 12 49337448 49337449 A G 20 GENIC homozygous 964860665 12 49338137 49338138 G T 31 GENIC homozygous 964860666 12 49339394 49339395 G C 6 GENIC homozygous 964860667 12 49339446 49339447 C G 8 GENIC homozygous 964860668 12 49340050 49340051 T C 14 GENIC homozygous 964860669 12 49341000 49341001 T C 17 GENIC homozygous 964860670 12 49341210 49341211 C T 22 GENIC homozygous 964860671 12 49369810 49369811 G A 27 GENIC homozygous 964860672 12 49370024 49370025 C T 20 GENIC homozygous 964860673 12 49372606 49372607 G A 41 GENIC homozygous 964860674 12 49376541 49376542 A G 31 GENIC homozygous 964860675 12 49386849 49386850 A G 24 GENIC homozygous 964860676 12 49394909 49394910 G A 18 GENIC homozygous 964860677