chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
X
7379875
7379876
A
-
4
GENIC
homozygous
45251031
X
7380941
7380942
T
TA
14
GENIC
homozygous
45082712
X
7389369
7389370
T
TC
2
GENIC
homozygous
45082715
X
7395373
7395374
T
TTGTG
5
GENIC
homozygous
45498375
X
7404024
7404025
T
C
6
GENIC
heterozygous
45082731
X
7413056
7413057
C
CATAG
4
GENIC
homozygous
45795264
X
7420680
7420681
G
T
8
GENIC
homozygous
45082741
X
7420686
7420687
G
T
7
GENIC
homozygous
45082742
X
7420690
7420691
T
-
7
GENIC
homozygous
45082743
X
7433665
7433666
T
-
2
GENIC
homozygous
45082746
X
7436725
7436726
A
-
5
GENIC
homozygous
45251035
X
7437042
7437043
A
C
8
GENIC
homozygous
45662436
X
7381718
7381719
C
T
17
GENIC
homozygous
45662427
X
7391568
7391569
A
AT
5
GENIC
homozygous
45662428
X
7404069
7404070
T
C
10
GENIC
homozygous
45662429
X
7418485
7418486
A
ATTTCTTTCTTTC
1
GENIC
homozygous
45662432
X
7418634
7418635
C
CGTGT
4
GENIC
homozygous
45662433
X
7431235
7431236
A
T
24
GENIC
homozygous
45662434
X
7432921
7432927
TGTGTG
------
1
GENIC
homozygous
45662435
X
7432389
7432390
G
GGGACAGTGGGGCATAGCACACATCTCATTTT
12
GENIC
heterozygous
45646699
