chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 143485641 143485642 C CA 5 GENIC heterozygous 768841363 5 143485641 143485642 C CAAA 5 GENIC heterozygous 768841364 5 143487391 143487392 A G 17 GENIC homozygous 670802082 5 143489159 143489160 A C 17 GENIC possibly homozygous 670802083 5 143489322 143489323 G A 16 GENIC homozygous 670802084 5 143489800 143489801 C T 20 GENIC homozygous 670802085 5 143491429 143491430 A G 19 GENIC possibly homozygous 670802086 5 143492236 143492237 C T 25 GENIC heterozygous 670802087 5 143492550 143492551 G A 12 GENIC homozygous 670802088 5 143494974 143494975 C T 21 GENIC homozygous 670802089 5 143500737 143500739 TA -- 8 GENIC heterozygous 768841366 5 143508606 143508607 G A 4 GENIC heterozygous 670802090 5 143512197 143512198 C T 19 GENIC heterozygous 670802091 5 143512403 143512404 T C 20 GENIC possibly homozygous 670802092 5 143514376 143514377 A C 13 GENIC homozygous 670802093 5 143514977 143514978 T C 17 GENIC homozygous 670802094 5 143516152 143516153 G GT 8 GENIC heterozygous 768841371 5 143518310 143518311 T C 20 GENIC possibly homozygous 670802095 5 143523066 143523067 C T 19 GENIC homozygous 670802096 5 143524691 143524692 C T 10 GENIC homozygous 670802097 5 143525318 143525319 G A 13 GENIC heterozygous 670802098 5 143526655 143526656 A G 22 GENIC possibly homozygous 670802099 5 143527141 143527142 A C 8 GENIC heterozygous 670802100 5 143527184 143527185 C A 8 GENIC possibly homozygous 670802101 5 143527395 143527396 T C 13 GENIC possibly homozygous 670802102 5 143529368 143529369 C T 23 GENIC homozygous 670802103 5 143531328 143531329 T C 11 GENIC possibly homozygous 670802104 5 143532111 143532112 T TTTTG 5 GENIC heterozygous 768841372