chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 139690012 139690013 C T 19 GENIC homozygous 803073792 5 139693004 139693005 G A 7 GENIC heterozygous 803073793 5 139694090 139694091 G A 15 GENIC heterozygous 803073794 5 139694279 139694280 A C 32 GENIC homozygous 803073795 5 139694442 139694443 G A 25 GENIC homozygous 803073796 5 139694920 139694921 C T 12 GENIC homozygous 803073797 5 139696549 139696550 A G 25 GENIC homozygous 803073798 5 139697356 139697357 C T 23 GENIC homozygous 803073799 5 139697456 139697457 A T 24 GENIC homozygous 803073800 5 139697670 139697671 G A 15 GENIC homozygous 803073801 5 139700094 139700095 C T 13 GENIC homozygous 803073802 5 139701742 139701743 T C 29 GENIC homozygous 803073803 5 139709936 139709937 C T 22 GENIC homozygous 803073804 5 139711213 139711214 G A 19 GENIC possibly homozygous 803073805 5 139717152 139717153 C T 17 GENIC possibly homozygous 803073806 5 139724327 139724328 T A 15 GENIC homozygous 803073807 5 139724858 139724859 C G 7 GENIC homozygous 803073808 5 139727912 139727913 T A 20 GENIC homozygous 803073809 5 139733451 139733452 A G 21 GENIC homozygous 803073810 5 139733937 139733938 A C 13 GENIC homozygous 803073811 5 139734191 139734192 T C 12 GENIC homozygous 803073812 5 139735976 139735977 A T 15 GENIC homozygous 803073813 5 139736164 139736165 C T 15 GENIC homozygous 803073814