chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 26903419 26903420 G A 22 GENIC homozygous 998180557 13 26904550 26904551 T G 21 GENIC homozygous 998180558 13 26904874 26904875 T C 20 GENIC homozygous 998180559 13 26905025 26905026 T C 31 GENIC homozygous 998180560 13 26905797 26905798 A G 20 GENIC homozygous 998180561 13 26906433 26906434 G A 38 GENIC homozygous 998180562 13 26906463 26906464 A C 37 GENIC homozygous 998180563 13 26907722 26907723 C T 29 GENIC homozygous 998180564 13 26907995 26907996 C T 30 GENIC homozygous 998180565 13 26908064 26908065 T C 20 GENIC homozygous 998180566 13 26908290 26908291 G A 24 GENIC homozygous 998180567 13 26908712 26908713 T C 35 GENIC homozygous 998180568 13 26908888 26908889 C G 43 GENIC homozygous 998180569 13 26909309 26909310 C T 28 GENIC homozygous 998180570 13 26910269 26910270 G C 31 GENIC homozygous 998180571 13 26910932 26910933 G T 24 GENIC homozygous 998180572 13 26911090 26911091 G A 22 GENIC homozygous 998180573 13 26911332 26911333 G A 29 GENIC homozygous 998180574 13 26911648 26911649 C T 31 GENIC homozygous 998180575 13 26912450 26912451 T G 33 GENIC homozygous 998180576 13 26913662 26913663 G A 27 GENIC homozygous 998180577 13 26917177 26917178 C T 26 GENIC homozygous 998180578 13 26918672 26918673 C T 22 GENIC homozygous 998180579 13 26919968 26919969 A G 34 GENIC homozygous 998180580 13 26920039 26920040 A G 30 GENIC homozygous 998180581 13 26921223 26921224 C T 19 GENIC homozygous 998180582 13 26921761 26921762 T C 29 GENIC homozygous 998180583 13 26922323 26922324 G A 28 GENIC homozygous 998180584 13 26922385 26922386 A T 26 GENIC homozygous 998180585 13 26922561 26922562 T C 23 GENIC homozygous 998180586 13 26922576 26922577 C A 24 GENIC homozygous 998180587 13 26922715 26922716 A C 25 GENIC homozygous 998180588 13 26922767 26922768 A G 23 GENIC homozygous 998180589