chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 98024392 98024393 T C 26 GENIC homozygous 994907349 13 98025675 98025676 C T 33 GENIC homozygous 994907350 13 98028596 98028597 T C 29 GENIC homozygous 994907351 13 98029041 98029042 C T 27 GENIC homozygous 994907352 13 98036270 98036271 A C 25 GENIC possibly homozygous 994907353 13 98036359 98036360 T C 23 GENIC possibly homozygous 994907354 13 98037390 98037391 T C 24 GENIC homozygous 994907355 13 98037544 98037545 G C 39 GENIC possibly homozygous 994907356 13 98038624 98038625 C T 36 GENIC possibly homozygous 994907357 13 98040671 98040672 T A 34 GENIC possibly homozygous 994907358 13 98042978 98042979 C T 17 GENIC homozygous 994907359 13 98044278 98044279 G A 17 GENIC homozygous 994907360 13 98044385 98044386 T C 18 GENIC possibly homozygous 994907361 13 98045840 98045841 C T 36 GENIC possibly homozygous 994907362 13 98046554 98046555 G C 33 GENIC possibly homozygous 994907363 13 98048084 98048085 C T 36 GENIC possibly homozygous 994907364 13 98049854 98049855 G T 35 GENIC possibly homozygous 994907365 13 98051449 98051450 A T 33 GENIC homozygous 994907366 13 98051872 98051873 T C 30 GENIC possibly homozygous 994907367 13 98051977 98051978 A T 26 GENIC possibly homozygous 994907368 13 98053109 98053110 T C 34 GENIC possibly homozygous 994907369 13 98053597 98053598 C T 24 GENIC possibly homozygous 994907370 13 98053997 98053998 G T 25 GENIC possibly homozygous 994907371 13 98059731 98059732 G C 25 GENIC possibly homozygous 994907372 13 98061330 98061331 G A 9 GENIC homozygous 994907373 13 98063627 98063628 T C 30 GENIC possibly homozygous 994907374 13 98065605 98065606 C A 27 GENIC possibly homozygous 994907375 13 98065695 98065696 C T 27 GENIC homozygous 994907376 13 98066725 98066726 T A 24 GENIC possibly homozygous 994907377 13 98066978 98066979 A G 26 GENIC homozygous 994907378 13 98068140 98068141 C T 24 GENIC possibly homozygous 994907379 13 98069332 98069333 C T 25 GENIC homozygous 994907380 13 98069409 98069410 T C 24 GENIC homozygous 994907381 13 98069782 98069783 C G 31 GENIC possibly homozygous 994907382 13 98069784 98069785 C T 30 GENIC possibly homozygous 994907383 13 98070389 98070390 T A 16 GENIC homozygous 994907384 13 98070734 98070735 T C 29 GENIC possibly homozygous 994907385 13 98072191 98072192 A G 31 GENIC possibly homozygous 994907386 13 98072506 98072507 G A 26 GENIC possibly homozygous 994907387 13 98073733 98073734 T C 29 GENIC possibly homozygous 994907388 13 98076203 98076204 A G 27 GENIC homozygous 994907389 13 98076301 98076302 C T 22 GENIC homozygous 994907390 13 98078383 98078384 T C 15 GENIC possibly homozygous 994907391