chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
40186162
40186163
C
T
47
GENIC
homozygous
116568735
10
40186229
40186232
GGA
34
GENIC
homozygous
131091681
10
40186688
40186689
C
A
55
GENIC
homozygous
116568737
10
40187014
40187015
C
T
48
GENIC
homozygous
116568739
10
40187023
40187024
C
A
46
GENIC
homozygous
116568741
10
40187280
40187281
T
C
59
GENIC
homozygous
116568743
10
40187915
40187916
C
T
49
GENIC
homozygous
118065926
10
40187102
40187103
C
T
56
GENIC
homozygous
116763920
10
40188252
40188253
T
C
48
GENIC
homozygous
116763922
10
40189067
40189068
C
T
73
GENIC
homozygous
116763924
10
40192284
40192285
C
A
26
GENIC
homozygous
116763928
10
40187926
40187927
C
T
52
GENIC
homozygous
118097993
10
40192113
40192114
A
T
54
GENIC
homozygous
116870414
10
40193695
40193696
T
16
GENIC
homozygous
128809812
10
40193713
40193714
G
15
GENIC
homozygous
128809813
10
40193732
40193733
C
10
GENIC
homozygous
128809814
10
40193747
40193748
G
C
10
GENIC
homozygous
118081241
10
40194533
40194534
T
C
51
GENIC
homozygous
116763930
10
40194580
40194581
A
G
44
GENIC
homozygous
116568745
10
40195183
40195184
G
A
64
GENIC
homozygous
116763932
10
40195409
40195524
AACACTTAAGATTCTTTTTTTTTTTTTGGTTCTTTTTTTTCGGAACTAGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCAAGCCCC
36
GENIC
homozygous
131091682
10
40195923
40195924
T
C
52
GENIC
homozygous
116763934
10
40196189
40196190
G
A
59
GENIC
homozygous
116763936
10
40197546
40197547
C
T
73
GENIC
homozygous
116763938
10
40193794
40193795
G
A
3
GENIC
homozygous
131100914
