chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 115510739 115510740 G GC 3 GENIC homozygous 723170485 8 115515719 115515721 GT -- 6 GENIC homozygous 723170486 8 115550228 115550229 T TCCC 7 GENIC heterozygous 723170487 8 115557406 115557407 C CTTT 4 GENIC homozygous 723170489 8 115585814 115585815 T TC 8 GENIC homozygous 723170491 8 115601140 115601141 T A 16 GENIC homozygous 588723140 8 115605806 115605808 CA -- 7 GENIC heterozygous 723170493 8 115609356 115609357 C - 19 GENIC homozygous 723170494 8 115609358 115609359 T - 21 GENIC homozygous 723170495 8 115609361 115609362 A G 20 GENIC homozygous 588723141 8 115609364 115609365 G - 21 GENIC homozygous 723170496 8 115609367 115609369 GG -- 22 GENIC homozygous 723170497 8 115610717 115610718 T - 21 GENIC heterozygous 723170498 8 115631230 115631231 C - 7 GENIC heterozygous 723170499