chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 170597358 170597359 G A 66 GENIC homozygous 108376209 1 170597788 170597789 G A 61 GENIC homozygous 108376211 1 170598294 170598295 T C 72 GENIC possibly homozygous 108376213 1 170600154 170600155 C T 60 GENIC homozygous 108376215 1 170600834 170600835 C A 50 GENIC homozygous 108376217 1 170601709 170601710 A T 63 GENIC homozygous 108376219 1 170606236 170606237 A G 62 GENIC homozygous 108376223 1 170606965 170606966 C T 59 GENIC homozygous 108376227 1 170607688 170607689 C T 46 GENIC homozygous 108376229 1 170609062 170609063 C T 59 GENIC homozygous 108376231 1 170609109 170609110 T C 55 GENIC homozygous 108376234 1 170609945 170609946 T C 42 GENIC homozygous 108376236 1 170610794 170610795 A G 44 GENIC homozygous 108376238 1 170610870 170610871 C A 43 GENIC homozygous 108376240 1 170611061 170611062 C T 46 GENIC homozygous 108376242 1 170611828 170611829 C T 37 GENIC homozygous 108376244 1 170614080 170614081 A G 51 GENIC possibly homozygous 108376246 1 170615839 170615840 C T 48 GENIC homozygous 108376248 1 170616208 170616209 C T 45 GENIC homozygous 108376250 1 170616360 170616361 C T 37 GENIC homozygous 108376252 1 170619031 170619032 C T 48 GENIC homozygous 108376254 1 170619252 170619253 C T 43 GENIC homozygous 108376256 1 170620820 170620821 T G 53 GENIC homozygous 108376258 1 170621609 170621610 G A 39 GENIC homozygous 108376260 1 170615184 170615185 C 53 GENIC homozygous 127455559 1 170615343 170615344 G 53 GENIC homozygous 127455560 1 170622757 170622758 T C 38 GENIC homozygous 108376262 1 170625577 170625578 C T 58 GENIC homozygous 108376264 1 170626457 170626458 G A 50 GENIC homozygous 108376266 1 170628568 170628569 G A 24 GENIC homozygous 108376268 1 170628428 170628429 T A 38 GENIC homozygous 108958866 1 170626684 170626685 A T 4 GENIC homozygous 130848255 1 170626686 170626687 A T 3 GENIC heterozygous 130848256 1 170626688 170626689 A T 4 GENIC heterozygous 130848257