chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 129798708 129798709 C T 21 GENIC homozygous 976141318 7 129799658 129799659 G A 11 GENIC homozygous 976141319 7 129800613 129800614 C T 20 GENIC homozygous 976141320 7 129801117 129801118 A G 5 GENIC homozygous 976141321 7 129801936 129801937 G A 16 GENIC homozygous 976141322 7 129804694 129804695 T G 13 GENIC homozygous 976141323 7 129804776 129804777 T C 10 GENIC homozygous 976141324 7 129804821 129804822 G A 16 GENIC possibly homozygous 976141325 7 129805161 129805162 T C 23 GENIC homozygous 976141326 7 129805282 129805283 A G 28 GENIC homozygous 976141327 7 129805315 129805316 T C 25 GENIC homozygous 976141328 7 129805327 129805328 G T 23 GENIC homozygous 976141329 7 129806000 129806001 C T 36 GENIC homozygous 976141330 7 129806589 129806590 C T 23 GENIC possibly homozygous 976141331 7 129807333 129807334 G A 10 GENIC homozygous 976141332 7 129808777 129808778 C T 19 GENIC homozygous 976141333 7 129808911 129808912 G T 17 GENIC homozygous 976141334 7 129808987 129808988 A G 20 GENIC homozygous 976141335 7 129810795 129810796 C T 26 GENIC homozygous 976141336 7 129810829 129810830 G A 28 GENIC homozygous 976141337 7 129811223 129811224 A G 24 GENIC homozygous 976141338