chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
19
41676594
41676595
G
T
9
GENIC
possibly homozygous
109889717
19
41679173
41679174
A
G
19
GENIC
homozygous
109702381
19
41679389
41679390
C
T
22
GENIC
homozygous
109702383
19
41679549
41679550
T
G
23
GENIC
homozygous
109702385
19
41680054
41680054
G
14
GENIC
homozygous
129609391
19
41679957
41679963
TGGGGG
5
GENIC
homozygous
129609388
19
41680034
41680034
G
10
GENIC
homozygous
129609389
19
41680036
41680039
TAT
11
GENIC
homozygous
129609390
19
41680058
41680059
A
14
GENIC
homozygous
129609392
19
41680092
41680092
CTTGCCA
19
GENIC
homozygous
129609393
19
41680096
41680096
TGGG
20
GENIC
homozygous
129609394
19
41680122
41680122
T
24
GENIC
homozygous
129609395
19
41680143
41680144
C
23
GENIC
homozygous
129609396
19
41680163
41680163
C
22
GENIC
homozygous
129609397
19
41680279
41680280
T
G
16
GENIC
homozygous
109702387
19
41680327
41680328
C
T
11
GENIC
homozygous
109702389
19
41680678
41680679
A
G
23
GENIC
homozygous
109702391
19
41681008
41681009
A
G
17
GENIC
homozygous
109702393
19
41681460
41681461
A
G
22
GENIC
homozygous
109702395
19
41681596
41681596
TGT
23
GENIC
homozygous
129609399
19
41681652
41681660
GCCGGGGG
19
GENIC
homozygous
129609400
19
41681663
41681768
GGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAACCAAAAAAAAAAAAAAAGGACAAGCC
20
GENIC
homozygous
129609401
19
41682187
41682188
T
11
GENIC
homozygous
129609402
19
41682585
41682586
T
A
15
GENIC
homozygous
109702397
19
41683044
41683045
C
G
23
GENIC
homozygous
109702399
19
41683052
41683053
A
C
23
GENIC
homozygous
109702401
19
41683144
41683145
C
A
20
GENIC
homozygous
109702403
19
41683148
41683149
T
C
20
GENIC
homozygous
109702405
19
41683374
41683375
T
A
26
GENIC
possibly homozygous
109702407
19
41683656
41683657
A
22
GENIC
homozygous
129609403
19
41683657
41683658
T
G
22
GENIC
homozygous
109702409
19
41680088
41680089
G
A
19
GENIC
homozygous
109782225
19
41680089
41680090
G
A
19
GENIC
homozygous
109817114
