chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 26903419 26903420 G A 35 GENIC homozygous 980131350 13 26904550 26904551 T G 25 GENIC homozygous 980131351 13 26904874 26904875 T C 46 GENIC homozygous 980131352 13 26905025 26905026 T C 30 GENIC homozygous 980131353 13 26905797 26905798 A G 16 GENIC homozygous 980131354 13 26907722 26907723 C T 26 GENIC homozygous 980131355 13 26907995 26907996 C T 31 GENIC homozygous 980131356 13 26908064 26908065 T C 42 GENIC homozygous 980131357 13 26908290 26908291 G A 21 GENIC homozygous 980131358 13 26908712 26908713 T C 32 GENIC homozygous 980131359 13 26908888 26908889 C G 46 GENIC homozygous 980131360 13 26909309 26909310 C T 33 GENIC homozygous 980131361 13 26910269 26910270 G C 20 GENIC homozygous 980131362 13 26910932 26910933 G T 30 GENIC homozygous 980131363 13 26911090 26911091 G A 20 GENIC homozygous 980131364 13 26911332 26911333 G A 26 GENIC homozygous 980131365 13 26911648 26911649 C T 19 GENIC homozygous 980131366 13 26912450 26912451 T G 38 GENIC homozygous 980131367 13 26913662 26913663 G A 38 GENIC homozygous 980131368 13 26917177 26917178 C T 9 GENIC homozygous 980131369 13 26918672 26918673 C T 13 GENIC homozygous 980131370 13 26919968 26919969 A G 12 GENIC homozygous 980131371 13 26920039 26920040 A G 16 GENIC homozygous 980131372 13 26921223 26921224 C T 20 GENIC homozygous 980131373 13 26921761 26921762 T C 31 GENIC homozygous 980131374 13 26922323 26922324 G A 19 GENIC homozygous 980131375 13 26922385 26922386 A T 27 GENIC homozygous 980131376 13 26922561 26922562 T C 11 GENIC homozygous 980131377 13 26922576 26922577 C A 10 GENIC homozygous 980131378 13 26922715 26922716 A C 19 GENIC homozygous 980131379 13 26922767 26922768 A G 28 GENIC possibly homozygous 980131380