chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 120457525 120457526 A T 42 GENIC homozygous 138197327 7 120458023 120458024 G A 42 GENIC homozygous 147554912 7 120460230 120460231 C T 44 GENIC homozygous 147554913 7 120460309 120460310 C A 40 GENIC homozygous 138197329 7 120462689 120462690 C G 48 GENIC homozygous 138197332 7 120462698 120462699 C G 44 GENIC homozygous 147554914 7 120463346 120463347 A G 43 GENIC homozygous 138197333 7 120465190 120465191 C A 40 GENIC homozygous 138197336 7 120465313 120465313 TT 38 GENIC possibly homozygous 147551290 7 120466786 120466792 GTTCCT 36 GENIC homozygous 147551291 7 120466834 120466835 G A 42 GENIC homozygous 147554915 7 120467502 120467503 C T 53 GENIC homozygous 147554916 7 120467539 120467540 G A 50 GENIC homozygous 138197340 7 120467549 120467550 A G 49 GENIC homozygous 138197341 7 120469440 120469441 T C 34 GENIC homozygous 138197342 7 120469917 120469918 C T 34 GENIC homozygous 147554917 7 120470040 120470041 C G 33 GENIC homozygous 146201995 7 120471101 120471102 T C 41 GENIC homozygous 138197343 7 120471464 120471465 C T 31 GENIC homozygous 146201997 7 120475382 120475383 A G 42 GENIC homozygous 138197344 7 120477356 120477358 AT 33 GENIC homozygous 147551292 7 120478336 120478337 A G 39 GENIC homozygous 138197347 7 120478944 120478945 A G 43 GENIC homozygous 138197348 7 120478987 120478988 C T 51 GENIC homozygous 138197349 7 120479636 120479637 G A 43 GENIC homozygous 138197350 7 120480639 120480640 T C 22 GENIC homozygous 138197351 7 120481623 120481624 G A 37 GENIC homozygous 138197352 7 120482093 120482094 T C 39 GENIC homozygous 138197353 7 120482588 120482589 T A 50 GENIC homozygous 138197354 7 120466674 120466674 CT 43 GENIC homozygous 137977943 7 120464368 120464368 T 43 GENIC possibly homozygous 137977941