chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 47604193 47604194 A G 19 GENIC homozygous 986106320 13 47604483 47604484 C T 26 GENIC homozygous 986106321 13 47604490 47604491 C T 27 GENIC homozygous 986106322 13 47604629 47604630 A C 29 GENIC homozygous 986106323 13 47604888 47604889 T C 23 GENIC homozygous 986106324 13 47605725 47605726 G A 27 GENIC homozygous 986106325 13 47605764 47605765 G T 31 GENIC homozygous 986106326 13 47606154 47606155 A T 31 GENIC homozygous 986106327 13 47606901 47606902 C T 15 GENIC homozygous 986106328 13 47606905 47606906 G A 15 GENIC homozygous 986106329 13 47606934 47606935 A G 15 GENIC homozygous 986106330 13 47607019 47607020 A G 17 GENIC homozygous 986106331 13 47607027 47607028 G A 16 GENIC homozygous 986106332 13 47607282 47607283 G T 13 GENIC homozygous 986106333 13 47607289 47607290 C T 9 GENIC homozygous 986106334 13 47607456 47607457 A G 18 GENIC homozygous 986106335 13 47607457 47607458 G A 19 GENIC homozygous 986106336 13 47607530 47607531 G A 23 GENIC homozygous 986106337 13 47607534 47607535 G T 21 GENIC homozygous 986106338 13 47607591 47607592 G C 17 GENIC homozygous 986106339 13 47607616 47607617 G A 12 GENIC homozygous 986106340 13 47608281 47608282 A G 16 GENIC homozygous 986106341 13 47608742 47608743 A G 22 GENIC homozygous 986106342 13 47611073 47611074 A G 13 GENIC homozygous 986106343 13 47611158 47611159 C T 21 GENIC homozygous 986106344 13 47612899 47612900 G A 18 GENIC homozygous 986106345