chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
19
37649347
37649348
G
A
31
GENIC
homozygous
140452555
19
37649428
37649429
G
A
37
GENIC
homozygous
140452556
19
37649790
37649791
C
T
35
GENIC
homozygous
140452557
19
37652771
37652772
C
T
54
GENIC
homozygous
140452558
19
37654282
37654283
T
29
GENIC
homozygous
403450672
19
37654282
37654283
T
A
29
GENIC
heterozygous
403450673
19
37654567
37654568
A
C
44
GENIC
homozygous
140452559
19
37658877
37658878
C
G
50
GENIC
homozygous
140452560
19
37659582
37659583
G
A
43
GENIC
homozygous
140452561
19
37659630
37659631
C
T
41
GENIC
homozygous
140452562
19
37664889
37664890
G
A
37
GENIC
homozygous
140452563
19
37665291
37665292
C
G
42
GENIC
homozygous
140452564
19
37665950
37665951
T
G
22
GENIC
homozygous
140452565
19
37666283
37666284
G
A
46
GENIC
homozygous
140452566
19
37666306
37666307
A
G
50
GENIC
homozygous
140452567
19
37668354
37668355
T
C
37
GENIC
homozygous
140452568
19
37669866
37669867
A
G
36
GENIC
homozygous
140452569
19
37664769
37664771
TA
33
GENIC
possibly homozygous
140388599
19
37654476
37654504
AATAAAGGGAAGCTCTTGTTTTCAGGAA
29
GENIC
homozygous
140388597
19
37656543
37656546
CTC
43
GENIC
homozygous
140388598