chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 30414992 30414993 T - 7 GENIC heterozygous 48122884 17 30415004 30415005 C T 8 GENIC heterozygous 48122885 17 30415087 30415088 G T 8 GENIC homozygous 47079327 17 30415105 30415106 G A 10 GENIC homozygous 47079328 17 30415132 30415133 C T 7 GENIC homozygous 47079329 17 30415135 30415136 C A 8 GENIC homozygous 47079330 17 30427002 30427003 A C 7 GENIC homozygous 47079388 17 30427013 30427014 G C 9 GENIC homozygous 47079389 17 30436402 30436403 C CA 16 GENIC homozygous 47079441 17 30436405 30436406 A T 16 GENIC homozygous 47319862 17 30436408 30436409 T - 16 GENIC homozygous 47079442 17 30472363 30472364 G GT 11 GENIC homozygous 47079501 17 30499957 30499959 AT -- 18 GENIC possibly homozygous 48122886 17 30519248 30519249 T - 19 GENIC homozygous 47079568 17 30519255 30519256 A T 18 GENIC homozygous 47079569 17 30519312 30519313 C - 19 GENIC homozygous 47079570 17 30519324 30519325 G - 20 GENIC homozygous 47079571 17 30527460 30527461 C CA 14 GENIC homozygous 47079608