chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 61463325 61463326 C CT 10 GENIC heterozygous 51470875 10 61466219 61466220 G GT 2 GENIC homozygous 51470876 10 61469592 61469593 C CA 17 GENIC possibly homozygous 51470879 10 61477979 61477980 C T 13 GENIC heterozygous 51470881 10 61484739 61484740 T TA 7 GENIC homozygous 51470884 10 61488072 61488073 T A 20 GENIC possibly homozygous 51470887 10 61490421 61490427 TCTCTC ------ 3 GENIC homozygous 51470888 10 61533510 61533512 GC -- 2 GENIC homozygous 52319782 10 61533557 61533558 G C 1 GENIC homozygous 51470891 10 61533558 61533559 A T 1 GENIC homozygous 51470892 10 61533562 61533563 C T 1 GENIC homozygous 51470893 10 61533563 61533564 A T 1 GENIC homozygous 51470894 10 61533567 61533568 G A 1 GENIC homozygous 51470895 10 61533689 61533690 A G 2 GENIC heterozygous 52380001 10 61539484 61539485 G GT 2 GENIC heterozygous 51470901 10 61544283 61544284 C A 24 GENIC possibly homozygous 51470902 10 61546108 61546109 C CA 16 GENIC homozygous 51470903 10 61551119 61551120 A G 12 GENIC possibly homozygous 51470904 10 61552224 61552225 A G 22 GENIC homozygous 51470905 10 61552903 61552904 G A 24 GENIC homozygous 51470906 10 61554036 61554037 G T 13 GENIC homozygous 51470907 10 61554254 61554255 G T 13 GENIC homozygous 51470908 10 61556841 61556842 C CTGTGTG 1 GENIC homozygous 52564061 10 61565333 61565334 G GA 7 GENIC possibly homozygous 51470911 10 61565424 61565425 T TACA 2 GENIC heterozygous 51470912 10 61567916 61567917 G T 3 GENIC homozygous 51470913 10 61568700 61568701 T C 7 GENIC possibly homozygous 51470914