chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 210999273 210999274 G C 38 GENIC homozygous 510253693 4 210999289 210999296 ACCAGGC ------- 19 GENIC homozygous 685581016 4 210999699 210999700 T C 57 GENIC homozygous 506635933 4 210999739 210999740 T C 69 GENIC homozygous 506635934 4 211000292 211000293 T A 58 GENIC homozygous 506635935 4 211000306 211000307 A G 57 GENIC homozygous 506635936 4 211000436 211000438 GT -- 43 GENIC homozygous 685581017 4 211000448 211000449 C A 45 GENIC homozygous 510253694 4 211001064 211001065 T C 70 GENIC homozygous 506635937 4 211001945 211001946 C T 59 GENIC possibly homozygous 510253695 4 211002129 211002130 A T 45 GENIC homozygous 506635938 4 211002190 211002191 G A 40 GENIC homozygous 506635939 4 211002241 211002242 T TCGAA 38 GENIC homozygous 685581018 4 211002372 211002373 C CCATGGGCCG 19 GENIC homozygous 685581019