chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 16918365 16918373 TCTCTCTG 24 GENIC homozygous 132523639 1 16926743 16926744 C 38 GENIC homozygous 127361358 1 16926777 16926777 T 35 GENIC homozygous 127361359 1 16926830 16926832 TT 34 GENIC homozygous 127361360 1 16926881 16926882 T 39 GENIC homozygous 127361361 1 16926896 16926896 G 42 GENIC homozygous 127361362 1 16926986 16926987 T 39 GENIC homozygous 127361363 1 16927000 16927001 G 35 GENIC homozygous 127361364 1 16927099 16927100 C 21 GENIC homozygous 127361365 1 16927115 16927115 C 29 GENIC homozygous 127361366 1 16927144 16927145 C 31 GENIC homozygous 127361367 1 16927212 16927212 G 31 GENIC homozygous 127361368 1 16927225 16927225 AA 28 GENIC homozygous 127361369 1 16927235 16927236 C 32 GENIC homozygous 127361370 1 16927237 16927238 A 32 GENIC homozygous 127361371 1 16927266 16927268 CG 31 GENIC homozygous 127361372 1 16927286 16927287 A 30 GENIC homozygous 127361373