chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 55266982 55266983 G T 25 GENIC homozygous 959029984 13 55267002 55267003 G A 19 GENIC homozygous 959029985 13 55270744 55270745 G T 23 GENIC homozygous 959029986 13 55270939 55270940 T C 21 GENIC homozygous 959029987 13 55271083 55271084 G T 27 GENIC homozygous 959029988 13 55271089 55271090 G A 27 GENIC homozygous 959029989 13 55271105 55271106 G C 25 GENIC homozygous 959029990 13 55271413 55271414 T C 27 GENIC homozygous 959029991 13 55271432 55271433 A G 30 GENIC homozygous 959029992 13 55271705 55271706 G T 19 GENIC homozygous 959029993 13 55271860 55271861 C G 21 GENIC homozygous 959029994 13 55271983 55271984 T A 23 GENIC homozygous 959029995 13 55272103 55272104 A G 29 GENIC homozygous 959029996 13 55272161 55272162 A G 34 GENIC homozygous 959029997 13 55272651 55272652 A G 26 GENIC homozygous 959029998 13 55272655 55272656 A C 26 GENIC homozygous 959029999 13 55272856 55272857 A G 12 GENIC homozygous 959030000 13 55273045 55273046 A G 10 GENIC homozygous 959030001 13 55273299 55273300 C T 20 GENIC homozygous 959030002 13 55273725 55273726 A C 24 GENIC homozygous 959030003 13 55276310 55276311 G A 21 GENIC homozygous 959030004 13 55281554 55281555 G A 32 GENIC homozygous 959030005 13 55283631 55283632 T C 19 GENIC homozygous 959030006 13 55284064 55284065 C T 28 GENIC homozygous 959030007 13 55285760 55285761 G T 31 GENIC homozygous 959030008