chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 61916465 61916466 T C 10 GENIC homozygous 112670966 4 61917262 61917263 G A 18 GENIC homozygous 112670976 4 61917470 61917471 G A 20 GENIC homozygous 112670980 4 61917989 61917990 T C 26 GENIC homozygous 113345454 4 61922084 61922085 A T 20 GENIC homozygous 112670988 4 61922130 61922131 G A 22 GENIC homozygous 112670990 4 61922952 61922953 G A 30 GENIC homozygous 112670994 4 61925346 61925347 A G 34 GENIC homozygous 112671005 4 61925549 61925550 G C 22 GENIC homozygous 112671007 4 61925849 61925850 G A 18 GENIC homozygous 112671009 4 61925997 61925998 A G 17 GENIC homozygous 112671011 4 61926415 61926416 G A 16 GENIC homozygous 112671013 4 61926921 61926922 C T 30 GENIC homozygous 113345456 4 61928139 61928140 A T 13 GENIC possibly homozygous 112671015 4 61928533 61928534 G A 13 GENIC homozygous 113345458 4 61928616 61928617 C T 7 GENIC homozygous 113345460