chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 3205218 3205219 G A 19 GENIC homozygous 973695430 14 3205225 3205226 G T 18 GENIC homozygous 973695431 14 3205664 3205665 C T 15 GENIC possibly homozygous 973695432 14 3206337 3206338 C A 17 GENIC homozygous 973695433 14 3208179 3208180 C T 8 GENIC homozygous 973695434 14 3213485 3213486 T G 19 GENIC homozygous 973695435 14 3215070 3215071 A G 14 GENIC homozygous 973695436 14 3215367 3215368 T C 21 GENIC homozygous 973695437 14 3216057 3216058 G A 25 GENIC homozygous 973695438 14 3216147 3216148 T A 24 GENIC homozygous 973695439 14 3216931 3216932 G T 18 GENIC homozygous 973695440 14 3218430 3218431 A G 36 GENIC homozygous 973695441 14 3220889 3220890 G A 28 GENIC homozygous 973695442 14 3220923 3220924 T C 25 GENIC homozygous 973695443 14 3221336 3221337 C T 13 GENIC homozygous 973695444 14 3222668 3222669 C T 30 GENIC homozygous 973695445 14 3222802 3222803 G T 24 GENIC homozygous 973695446 14 3223987 3223988 C T 26 GENIC homozygous 973695447 14 3225471 3225472 C T 21 GENIC homozygous 973695448 14 3229301 3229302 T C 27 GENIC homozygous 973695449 14 3230906 3230907 T G 11 GENIC homozygous 973695450 14 3230908 3230909 T G 12 GENIC homozygous 973695451 14 3231498 3231499 T C 23 GENIC homozygous 973695452 14 3232109 3232110 A C 24 GENIC homozygous 973695453 14 3242821 3242822 A C 13 GENIC homozygous 973695454 14 3245150 3245151 C T 16 GENIC homozygous 973695455 14 3245515 3245516 G A 17 GENIC homozygous 973695456 14 3245589 3245590 A G 28 GENIC homozygous 973695457 14 3245684 3245685 G A 39 GENIC homozygous 973695458 14 3246568 3246569 T C 26 GENIC homozygous 973695459 14 3246909 3246910 A G 31 GENIC homozygous 973695460 14 3247015 3247016 T C 25 GENIC homozygous 973695461