chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 59595061 59595062 T C 58 GENIC homozygous 52664068 8 59596396 59596397 T G 48 GENIC homozygous 52983288 8 59596828 59596829 T A 5 GENIC homozygous 52664070 8 59596829 59596830 T G 5 GENIC homozygous 52664072 8 59596834 59596835 T TG 5 GENIC homozygous 52664074 8 59596884 59596885 C A 18 GENIC homozygous 52664076 8 59596887 59596889 AA -- 8 GENIC possibly homozygous 52983289 8 59597350 59597351 C T 52 GENIC homozygous 52983290 8 59597430 59597431 C CAA 44 GENIC possibly homozygous 52664080 8 59597430 59597431 C CA 44 GENIC heterozygous 52664082 8 59597430 59597431 C CAAA 44 GENIC heterozygous 52983291 8 59598668 59598669 A - 65 GENIC homozygous 52983292 8 59603281 59603282 A G 60 GENIC homozygous 52664084 8 59603988 59603989 T C 50 GENIC homozygous 52664086 8 59605092 59605093 T - 2 GENIC homozygous 52664090 8 59605239 59605240 T - 54 GENIC homozygous 52664092 8 59607059 59607060 C T 48 GENIC homozygous 52983293