geneid | 11064 |
---|---|
ensemblid | ENSG00000119397.19 |
hgncid | 1858 |
symbol | CNTRL |
name | centriolin |
refseq_nuc | NM_007018.6 |
refseq_prot | NP_008949.4 |
ensembl_nuc | ENST00000373855.7 |
ensembl_prot | ENSP00000362962.1 |
mane_status | MANE Select |
chr | chr9 |
start | 121074955 |
end | 121177610 |
strand | + |
ver | v1.2 |
region | chr9:121074955-121177610 |
region5000 | chr9:121069955-121182610 |
regionname0 | CNTRL_chr9_121074955_121177610 |
regionname5000 | CNTRL_chr9_121069955_121182610 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2325 | 107 | 47 | 18 | 37 | 3 | 0 | 24 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0002 | 0/0 | 2325 | 96 | 11 | 19 | 50 | 5 | 11 | 40 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0003 | 0/0 | 2325 | 85 | 9 | 18 | 44 | 3 | 11 | 38 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0004 | 0/0 | 2325 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0005 | 0/0 | 2325 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0006 | 0/0 | 2325 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0007 | 0/0 | 2325 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0008 | 0/0 | 2325 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0009 | 0/0 | 2325 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0010 | 0/0 | 2325 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0011 | 0/0 | 2325 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0012 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0013 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0014 | 0/0 | 2325 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0015 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0016 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0017 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0018 | 0/0 | 2325 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0019 | 0/0 | 2325 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0020 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0021 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0022 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0023 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0024 | 0/0 | 2325 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0025 | 0/0 | 2325 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0026 | 0/0 | 2325 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 6978 | 90 | 42 | 10 | 35 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0002 | 0/0 | 6978 | 85 | 2 | 18 | 49 | 5 | 11 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0003 | 0/0 | 6978 | 68 | 3 | 14 | 40 | 2 | 9 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0004 | 0/0 | 6978 | 16 | 6 | 4 | 3 | 1 | 2 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0005 | 0/0 | 6978 | 12 | 4 | 4 | 2 | 2 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0006 | 0/0 | 6978 | 10 | 9 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0007 | 0/0 | 6978 | 6 | 6 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0008 | 0/0 | 6978 | 5 | 0 | 0 | 5 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0009 | 0/0 | 6978 | 4 | 0 | 4 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0010 | 0/0 | 6978 | 3 | 0 | 1 | 0 | 0 | 2 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0011 | 0/0 | 6978 | 3 | 0 | 3 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0012 | 0/0 | 6978 | 3 | 3 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0013 | 0/0 | 6978 | 2 | 0 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0014 | 0/0 | 6978 | 2 | 2 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0015 | 0/0 | 6978 | 2 | 0 | 0 | 0 | 2 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0016 | 0/0 | 6978 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0017 | 0/0 | 6978 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0018 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0019 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0020 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0021 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0022 | 0/0 | 6978 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0023 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0024 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0025 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0026 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0027 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0028 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0029 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0030 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0031 | 0/0 | 6978 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0032 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0033 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
c0034 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 742 | 300 | 69 | 59 | 137 | 12 | 21 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
t0002 | 0/0 | 743 | 21 | 8 | 4 | 5 | 2 | 2 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
t0003 | 0/0 | 740 | 8 | 7 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
t0004 | 0/0 | 742 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0161 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 6978 | 90 | 42 | 10 | 35 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0001c0005 | 0/0 | 6978 | 12 | 4 | 4 | 2 | 2 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0001c0009 | 0/0 | 6978 | 4 | 0 | 4 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0001c0032 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0002c0002 | 0/0 | 6978 | 85 | 2 | 18 | 49 | 5 | 11 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0002c0006 | 0/0 | 6978 | 10 | 9 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0002c0023 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0003c0003 | 0/0 | 6978 | 68 | 3 | 14 | 40 | 2 | 9 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0003c0004 | 0/0 | 6978 | 16 | 6 | 4 | 3 | 1 | 2 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0003c0019 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0004c0007 | 0/0 | 6978 | 6 | 6 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0004c0026 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0005c0008 | 0/0 | 6978 | 5 | 0 | 0 | 5 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0006c0010 | 0/0 | 6978 | 3 | 0 | 1 | 0 | 0 | 2 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0007c0011 | 0/0 | 6978 | 3 | 0 | 3 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0008c0012 | 0/0 | 6978 | 3 | 3 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0009c0015 | 0/0 | 6978 | 2 | 0 | 0 | 0 | 2 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0010c0014 | 0/0 | 6978 | 2 | 2 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0011c0013 | 0/0 | 6978 | 2 | 0 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0012c0025 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0013c0021 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0014c0022 | 0/0 | 6978 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0015c0024 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0016c0020 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0017c0018 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0018c0017 | 0/0 | 6978 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0019c0016 | 0/0 | 6978 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0020c0034 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0021c0030 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0022c0028 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0023c0029 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0024c0031 | 0/0 | 6978 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0025c0027 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0026c0033 | 0/0 | 6978 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 7719 | 82 | 35 | 9 | 35 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0001c0001t0003 | 0/0 | 7717 | 8 | 7 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0001c0005t0001 | 0/0 | 7719 | 12 | 4 | 4 | 2 | 2 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0001c0009t0001 | 0/0 | 7719 | 4 | 0 | 4 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0001c0032t0001 | 0/0 | 7719 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0002c0002t0001 | 0/0 | 7719 | 83 | 2 | 18 | 48 | 5 | 10 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0002c0002t0002 | 0/0 | 7720 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0002c0002t0004 | 0/0 | 7719 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0002c0006t0001 | 0/0 | 7719 | 10 | 9 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0002c0023t0001 | 0/0 | 7719 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0003c0003t0001 | 0/0 | 7719 | 68 | 3 | 14 | 40 | 2 | 9 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0003c0004t0001 | 0/0 | 7719 | 2 | 1 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0003c0004t0002 | 0/0 | 7720 | 14 | 5 | 3 | 3 | 1 | 2 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0003c0019t0002 | 0/0 | 7720 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0004c0007t0001 | 0/0 | 7719 | 6 | 6 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0004c0026t0001 | 0/0 | 7719 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0005c0008t0001 | 0/0 | 7719 | 5 | 0 | 0 | 5 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0006c0010t0001 | 0/0 | 7719 | 3 | 0 | 1 | 0 | 0 | 2 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0007c0011t0001 | 0/0 | 7719 | 3 | 0 | 3 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0008c0012t0002 | 0/0 | 7720 | 3 | 3 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0009c0015t0001 | 0/0 | 7719 | 2 | 0 | 0 | 0 | 2 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0010c0014t0001 | 0/0 | 7719 | 2 | 2 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0011c0013t0001 | 0/0 | 7719 | 2 | 0 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0012c0025t0001 | 0/0 | 7719 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0013c0021t0001 | 0/0 | 7719 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0014c0022t0001 | 0/0 | 7719 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0015c0024t0001 | 0/0 | 7719 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0016c0020t0001 | 0/0 | 7719 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0017c0018t0001 | 0/0 | 7719 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0018c0017t0002 | 0/0 | 7720 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0019c0016t0002 | 0/0 | 7720 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0020c0034t0001 | 0/0 | 7719 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0021c0030t0001 | 0/0 | 7719 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0022c0028t0001 | 0/0 | 7719 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0023c0029t0001 | 0/0 | 7719 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0024c0031t0001 | 0/0 | 7719 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0025c0027t0001 | 0/0 | 7719 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
a0026c0033t0001 | 0/0 | 7719 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | copy fasta | chr9 | 121069955 | 121182610 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0161 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0005t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0005t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0005t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0005t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0005t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0005t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0005t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0005t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0005t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0009t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0009t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0009t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0001c0032t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0002t0004g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0006t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0006t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0006t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0006t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0006t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0006t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0006t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0006t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0006t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0002c0023t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0004t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0003c0019t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0004c0007t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0004c0007t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0004c0007t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0004c0007t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0004c0007t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0004c0026t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0005c0008t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0005c0008t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0005c0008t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0005c0008t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0005c0008t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0006c0010t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0006c0010t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0006c0010t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0007c0011t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0007c0011t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0008c0012t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0008c0012t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0008c0012t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0009c0015t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0009c0015t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0010c0014t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0010c0014t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0011c0013t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0011c0013t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0012c0025t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0013c0021t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0014c0022t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0015c0024t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0016c0020t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0017c0018t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0018c0017t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0019c0016t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0020c0034t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0021c0030t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0022c0028t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0023c0029t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0024c0031t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0025c0027t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
a0026c0033t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | GBR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00099 | hp2 | a0018 | c0017 | t0002 | g0126 | EUR | GBR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0096 | EUR | GBR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00140 | hp2 | a0003 | c0003 | t0001 | g0261 | EUR | GBR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00280 | hp1 | a0001 | c0005 | t0001 | g0184 | EUR | FIN | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0106 | EUR | FIN | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0055 | EUR | FIN | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00323 | hp2 | a0003 | c0004 | t0002 | g0009 | EUR | FIN | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00408 | hp1 | a0012 | c0025 | t0001 | g0111 | EAS | CHS | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00408 | hp2 | a0022 | c0028 | t0001 | g0212 | EAS | CHS | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00438 | hp1 | a0026 | c0033 | t0001 | g0170 | EAS | CHS | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00597 | hp2 | a0003 | c0003 | t0001 | g0294 | EAS | CHS | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | CHS | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00639 | hp2 | a0003 | c0004 | t0001 | g0140 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00738 | hp1 | a0024 | c0031 | t0001 | g0154 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00738 | hp2 | a0003 | c0004 | t0002 | g0133 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00741 | hp1 | a0003 | c0003 | t0001 | g0116 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01069 | hp2 | a0003 | c0003 | t0001 | g0260 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01070 | hp1 | a0006 | c0010 | t0001 | g0091 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01070 | hp2 | a0001 | c0005 | t0001 | g0003 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01071 | hp2 | a0001 | c0005 | t0001 | g0003 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0054 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0258 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01106 | hp1 | a0001 | c0009 | t0001 | g0013 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01106 | hp2 | a0003 | c0003 | t0001 | g0289 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01109 | hp2 | a0002 | c0006 | t0001 | g0026 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01167 | hp1 | a0011 | c0013 | t0001 | g0248 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01168 | hp1 | a0007 | c0011 | t0001 | g0014 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01168 | hp2 | a0003 | c0003 | t0001 | g0275 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01169 | hp1 | a0007 | c0011 | t0001 | g0014 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01169 | hp2 | a0011 | c0013 | t0001 | g0249 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01175 | hp2 | a0003 | c0004 | t0002 | g0134 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01192 | hp1 | a0001 | c0009 | t0001 | g0156 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01192 | hp2 | a0001 | c0005 | t0001 | g0003 | AMR | PUR | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0057 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01255 | hp2 | a0007 | c0011 | t0001 | g0162 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0086 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01256 | hp2 | a0003 | c0003 | t0001 | g0299 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0087 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0103 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01346 | hp1 | a0003 | c0003 | t0001 | g0020 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01346 | hp2 | a0001 | c0009 | t0001 | g0013 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0270 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0110 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0104 | EUR | IBS | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01515 | hp2 | a0009 | c0015 | t0001 | g0157 | EUR | IBS | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01517 | hp1 | a0009 | c0015 | t0001 | g0148 | EUR | IBS | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0065 | EUR | IBS | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01884 | hp1 | a0001 | c0005 | t0001 | g0174 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01884 | hp2 | a0003 | c0004 | t0002 | g0124 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01891 | hp1 | a0002 | c0006 | t0001 | g0023 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01891 | hp2 | a0001 | c0032 | t0001 | g0190 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01952 | hp1 | a0003 | c0003 | t0001 | g0279 | AMR | PEL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01952 | hp2 | a0001 | c0005 | t0001 | g0182 | AMR | PEL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01975 | hp1 | a0003 | c0003 | t0001 | g0257 | AMR | PEL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01975 | hp2 | a0001 | c0009 | t0001 | g0155 | AMR | PEL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0102 | AMR | PEL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01978 | hp2 | a0003 | c0003 | t0001 | g0278 | AMR | PEL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01981 | hp1 | a0003 | c0003 | t0001 | g0271 | AMR | PEL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01981 | hp2 | a0019 | c0016 | t0002 | g0021 | AMR | PEL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01993 | hp1 | a0003 | c0003 | t0001 | g0269 | AMR | PEL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0082 | AMR | PEL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02027 | hp1 | a0003 | c0004 | t0002 | g0125 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02027 | hp2 | a0003 | c0003 | t0001 | g0272 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02055 | hp1 | a0001 | c0005 | t0001 | g0185 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02056 | hp1 | a0003 | c0003 | t0001 | g0298 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02071 | hp1 | a0003 | c0003 | t0001 | g0302 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02083 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | KHV | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | CDX | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CDX | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02257 | hp2 | a0003 | c0003 | t0001 | g0117 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02280 | hp2 | a0002 | c0006 | t0001 | g0028 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02293 | hp1 | a0003 | c0004 | t0002 | g0132 | AMR | PEL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02293 | hp2 | a0014 | c0022 | t0001 | g0039 | AMR | PEL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02451 | hp1 | a0004 | c0007 | t0001 | g0137 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02572 | hp2 | a0021 | c0030 | t0001 | g0235 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02647 | hp2 | a0002 | c0006 | t0001 | g0032 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0051 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02698 | hp1 | a0006 | c0010 | t0001 | g0090 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02698 | hp2 | a0003 | c0003 | t0001 | g0291 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02717 | hp1 | a0025 | c0027 | t0001 | g0193 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02717 | hp2 | a0004 | c0007 | t0001 | g0010 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02809 | hp2 | a0010 | c0014 | t0001 | g0169 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02818 | hp2 | a0003 | c0004 | t0001 | g0122 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02886 | hp2 | a0004 | c0007 | t0001 | g0138 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02895 | hp1 | a0004 | c0007 | t0001 | g0136 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02896 | hp1 | a0001 | c0005 | t0001 | g0181 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02896 | hp2 | a0002 | c0006 | t0001 | g0029 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02897 | hp1 | a0001 | c0005 | t0001 | g0166 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02965 | hp1 | a0010 | c0014 | t0001 | g0167 | AFR | ESN | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | ESN | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | ESN | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02976 | hp1 | a0008 | c0012 | t0002 | g0142 | AFR | ESN | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0053 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03017 | hp2 | a0003 | c0004 | t0002 | g0129 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03098 | hp1 | a0004 | c0007 | t0001 | g0010 | AFR | MSL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | MSL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03130 | hp1 | a0008 | c0012 | t0002 | g0143 | AFR | ESN | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03130 | hp2 | a0002 | c0006 | t0001 | g0024 | AFR | ESN | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03225 | hp2 | a0004 | c0007 | t0001 | g0139 | AFR | MSL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03239 | hp1 | a0003 | c0003 | t0001 | g0251 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0099 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03486 | hp1 | a0004 | c0026 | t0001 | g0135 | AFR | MSL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03490 | hp1 | a0003 | c0003 | t0001 | g0018 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03490 | hp2 | a0006 | c0010 | t0001 | g0052 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0070 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03492 | hp2 | a0003 | c0003 | t0001 | g0018 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03540 | hp1 | a0003 | c0003 | t0001 | g0266 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03540 | hp2 | a0003 | c0004 | t0002 | g0128 | AFR | GWD | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03579 | hp1 | a0003 | c0004 | t0002 | g0123 | AFR | MSL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03579 | hp2 | a0013 | c0021 | t0001 | g0030 | AFR | MSL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03654 | hp1 | a0002 | c0002 | t0004 | g0001 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03654 | hp2 | a0003 | c0003 | t0001 | g0264 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0056 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03710 | hp2 | a0003 | c0003 | t0001 | g0265 | SAS | PJL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03831 | hp1 | a0003 | c0003 | t0001 | g0295 | SAS | BEB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03831 | hp2 | a0003 | c0003 | t0001 | g0268 | SAS | BEB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0058 | SAS | BEB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03834 | hp2 | a0003 | c0003 | t0001 | g0276 | SAS | BEB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0063 | SAS | BEB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0064 | SAS | BEB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18522 | hp1 | a0002 | c0006 | t0001 | g0025 | AFR | YRI | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18939 | hp1 | a0003 | c0003 | t0001 | g0255 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18941 | hp1 | a0003 | c0003 | t0001 | g0253 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18943 | hp1 | a0003 | c0003 | t0001 | g0303 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18943 | hp2 | a0002 | c0023 | t0001 | g0092 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18944 | hp1 | a0003 | c0003 | t0001 | g0290 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18946 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18948 | hp1 | a0003 | c0004 | t0002 | g0131 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18948 | hp2 | a0003 | c0003 | t0001 | g0280 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18950 | hp1 | a0005 | c0008 | t0001 | g0077 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18951 | hp1 | a0003 | c0003 | t0001 | g0288 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18952 | hp1 | a0003 | c0003 | t0001 | g0283 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18954 | hp2 | a0003 | c0003 | t0001 | g0118 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18959 | hp1 | a0003 | c0003 | t0001 | g0286 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18959 | hp2 | a0016 | c0020 | t0001 | g0115 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18964 | hp2 | a0003 | c0003 | t0001 | g0259 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18967 | hp2 | a0003 | c0003 | t0001 | g0305 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18968 | hp2 | a0003 | c0003 | t0001 | g0297 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18969 | hp1 | a0003 | c0003 | t0001 | g0285 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18971 | hp2 | a0001 | c0005 | t0001 | g0015 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18975 | hp2 | a0003 | c0003 | t0001 | g0277 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18977 | hp1 | a0005 | c0008 | t0001 | g0073 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18977 | hp2 | a0003 | c0003 | t0001 | g0292 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18978 | hp2 | a0023 | c0029 | t0001 | g0224 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18979 | hp1 | a0017 | c0018 | t0001 | g0293 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18982 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18985 | hp1 | a0005 | c0008 | t0001 | g0094 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18985 | hp2 | a0003 | c0003 | t0001 | g0267 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18986 | hp1 | a0003 | c0003 | t0001 | g0273 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18990 | hp1 | a0005 | c0008 | t0001 | g0076 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18990 | hp2 | a0003 | c0003 | t0001 | g0301 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18991 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18992 | hp2 | a0003 | c0003 | t0001 | g0282 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18997 | hp2 | a0003 | c0003 | t0001 | g0274 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18999 | hp2 | a0003 | c0003 | t0001 | g0119 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19003 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19004 | hp2 | a0003 | c0003 | t0001 | g0263 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19006 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19006 | hp2 | a0003 | c0003 | t0001 | g0304 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19010 | hp2 | a0003 | c0003 | t0001 | g0284 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19012 | hp2 | a0001 | c0005 | t0001 | g0015 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | LWK | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19043 | hp1 | a0003 | c0003 | t0001 | g0262 | AFR | LWK | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19043 | hp2 | a0015 | c0024 | t0001 | g0031 | AFR | LWK | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19058 | hp2 | a0003 | c0003 | t0001 | g0252 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19062 | hp2 | a0003 | c0004 | t0002 | g0130 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19063 | hp1 | a0003 | c0003 | t0001 | g0256 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19070 | hp1 | a0005 | c0008 | t0001 | g0062 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19074 | hp2 | a0003 | c0003 | t0001 | g0254 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19076 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19076 | hp2 | a0003 | c0003 | t0001 | g0300 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0287 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA19090 | hp2 | a0003 | c0003 | t0001 | g0281 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA20129 | hp1 | a0002 | c0006 | t0001 | g0027 | AFR | ASW | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ASW | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA20752 | hp1 | a0003 | c0003 | t0001 | g0250 | EUR | TSI | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA20752 | hp2 | a0001 | c0005 | t0001 | g0183 | EUR | TSI | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA20905 | hp1 | a0003 | c0004 | t0002 | g0009 | SAS | GIH | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0095 | SAS | GIH | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG01123 | hp2 | a0003 | c0003 | t0001 | g0020 | AMR | CLM | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02486 | hp1 | a0003 | c0004 | t0002 | g0141 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0067 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG02559 | hp2 | a0003 | c0004 | t0002 | g0145 | AFR | ACB | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03471 | hp1 | a0002 | c0006 | t0001 | g0033 | AFR | MSL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG03471 | hp2 | a0020 | c0034 | t0001 | g0168 | AFR | MSL | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | USA | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
HG06807 | hp2 | a0008 | c0012 | t0002 | g0144 | AFR | USA | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18955 | hp1 | a0003 | c0003 | t0001 | g0296 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA18955 | hp2 | a0003 | c0019 | t0002 | g0127 | EAS | JPT | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0079 | AFR | USA | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | USA | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | LWK | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
NA21309 | hp2 | a0002 | c0006 | t0001 | g0146 | AFR | LWK | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0173 | REF | REF | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0161 | REF | REF | CNTRL_chr9_121069955_121182610 | CNTRL | chr9 | 121069955 | 121182610 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:121088364
|
C | A | 1 | a0011 | 2 | HG01167.hp1 HG01169.hp2 |
missense_variant | MODERATE | c.38C>A | p.Ala13Glu | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/44 | 355/7719 | 38/6978 | 13/2325 | chr9 | 121088364 | ||
chr9:121088441
|
A | G | 1 | a0008 | 3 | HG02976.hp1 HG03130.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.115A>G | p.Ile39Val | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/44 | 432/7719 | 115/6978 | 39/2325 | chr9 | 121088441 | ||
chr9:121088492
|
G | A | 14 | a0002a0003a0005others(11): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
missense_variant | MODERATE | c.166G>A | p.Val56Ile | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/44 | 483/7719 | 166/6978 | 56/2325 | chr9 | 121088492 | ||
chr9:121098411
|
C | T | 9 | a0002a0005a0006others(6): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
missense_variant | MODERATE | c.647C>T | p.Pro216Leu | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/44 | 964/7719 | 647/6978 | 216/2325 | chr9 | 121098411 | ||
chr9:121113643
|
C | G | 1 | a0007 | 3 | HG01168.hp1 HG01169.hp1 HG01255.hp2 |
missense_variant | MODERATE | c.1264C>G | p.Leu422Val | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 10/44 | 1581/7719 | 1264/6978 | 422/2325 | chr9 | 121113643 | ||
chr9:121113689
|
C | T | 1 | a0020 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.1310C>T | p.Thr437Met | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 10/44 | 1627/7719 | 1310/6978 | 437/2325 | chr9 | 121113689 | ||
chr9:121118362
|
A | G | 1 | a0026 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1472A>G | p.Lys491Arg | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/44 | 1789/7719 | 1472/6978 | 491/2325 | chr9 | 121118362 | ||
chr9:121118416
|
G | A | 1 | a0004 | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
missense_variant | MODERATE | c.1526G>A | p.Arg509His | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/44 | 1843/7719 | 1526/6978 | 509/2325 | chr9 | 121118416 | ||
chr9:121118416
|
G | T | 1 | a0012 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.1526G>T | p.Arg509Leu | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/44 | 1843/7719 | 1526/6978 | 509/2325 | chr9 | 121118416 | ||
chr9:121125843
|
T | G | 1 | a0016 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.1932T>G | p.Asp644Glu | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/44 | 2249/7719 | 1932/6978 | 644/2325 | chr9 | 121125843 | ||
chr9:121135981
|
A | G | 1 | a0015 | 1 | NA19043.hp2 | missense_variant&splice_region_variant | MODERATE | c.2201A>G | p.Gln734Arg | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/44 | 2518/7719 | 2201/6978 | 734/2325 | chr9 | 121135981 | ||
chr9:121141562
|
G | A | 1 | a0006 | 3 | HG01070.hp1 HG02698.hp1 HG03490.hp2 |
missense_variant | MODERATE | c.2665G>A | p.Ala889Thr | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 18/44 | 2982/7719 | 2665/6978 | 889/2325 | chr9 | 121141562 | ||
chr9:121142260
|
T | C | 1 | a0019 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.2861T>C | p.Leu954Ser | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 19/44 | 3178/7719 | 2861/6978 | 954/2325 | chr9 | 121142260 | ||
chr9:121145244
|
T | G | 2 | a0010a0020 | 3 | HG02809.hp2 HG02965.hp1 HG03471.hp2 |
missense_variant&splice_region_variant | MODERATE | c.3169T>G | p.Phe1057Val | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 22/44 | 3486/7719 | 3169/6978 | 1057/2325 | chr9 | 121145244 | ||
chr9:121148780
|
G | A | 1 | a0025 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.3568G>A | p.Gly1190Ser | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 24/44 | 3885/7719 | 3568/6978 | 1190/2325 | chr9 | 121148780 | ||
chr9:121158065
|
C | G | 1 | a0024 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.4720C>G | p.Leu1574Val | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 30/44 | 5037/7719 | 4720/6978 | 1574/2325 | chr9 | 121158065 | ||
chr9:121164944
|
G | T | 1 | a0005 | 5 | NA18950.hp1 NA18977.hp1 NA18985.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.5425G>T | p.Val1809Phe | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 35/44 | 5742/7719 | 5425/6978 | 1809/2325 | chr9 | 121164944 | ||
chr9:121167505
|
C | A | 1 | a0013 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.5672C>A | p.Thr1891Asn | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 37/44 | 5989/7719 | 5672/6978 | 1891/2325 | chr9 | 121167505 | ||
chr9:121169751
|
A | G | 1 | a0021 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.6211A>G | p.Lys2071Glu | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/44 | 6528/7719 | 6211/6978 | 2071/2325 | chr9 | 121169751 | ||
chr9:121169757
|
G | C | 1 | a0022 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.6217G>C | p.Val2073Leu | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/44 | 6534/7719 | 6217/6978 | 2073/2325 | chr9 | 121169757 | ||
chr9:121169761
|
C | A | 1 | a0018 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.6221C>A | p.Ala2074Asp | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/44 | 6538/7719 | 6221/6978 | 2074/2325 | chr9 | 121169761 | ||
chr9:121173475
|
A | G | 1 | a0023 | 1 | NA18978.hp2 | missense_variant | MODERATE | c.6650A>G | p.Glu2217Gly | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 41/44 | 6967/7719 | 6650/6978 | 2217/2325 | chr9 | 121173475 | ||
chr9:121173702
|
C | T | 1 | a0017 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.6712C>T | p.Arg2238Trp | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 42/44 | 7029/7719 | 6712/6978 | 2238/2325 | chr9 | 121173702 | ||
chr9:121175073
|
G | T | 1 | a0014 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.6803G>T | p.Arg2268Leu | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/44 | 7120/7719 | 6803/6978 | 2268/2325 | chr9 | 121175073 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:121123999
|
A | G | 1 | a0001c0009 | 4 | HG01106.hp1 HG01192.hp1 HG01346.hp2 others(1): Show |
synonymous_variant | LOW | c.1719A>G | p.Gln573Gln | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/44 | 2036/7719 | 1719/6978 | 573/2325 | chr9 | 121123999 | ||
chr9:121138640
|
A | G | 1 | a0003c0019 | 1 | NA18955.hp2 | synonymous_variant | LOW | c.2298A>G | p.Gln766Gln | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/44 | 2615/7719 | 2298/6978 | 766/2325 | chr9 | 121138640 | ||
chr9:121150264
|
T | G | 5 | a0002c0006a0004c0007a0004c0026others(2): Show | 19 | HG01109.hp2 HG01891.hp1 HG02280.hp2 others(16): Show |
synonymous_variant | LOW | c.3744T>G | p.Thr1248Thr | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/44 | 4061/7719 | 3744/6978 | 1248/2325 | chr9 | 121150264 | ||
chr9:121152562
|
A | G | 1 | a0001c0032 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.4041A>G | p.Ala1347Ala | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 26/44 | 4358/7719 | 4041/6978 | 1347/2325 | chr9 | 121152562 | ||
chr9:121152596
|
C | T | 1 | a0001c0005 | 12 | HG00280.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
synonymous_variant | LOW | c.4075C>T | p.Leu1359Leu | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 26/44 | 4392/7719 | 4075/6978 | 1359/2325 | chr9 | 121152596 | ||
chr9:121154742
|
T | A | 11 | a0002c0002a0002c0006a0002c0023others(8): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
synonymous_variant | LOW | c.4194T>A | p.Val1398Val | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/44 | 4511/7719 | 4194/6978 | 1398/2325 | chr9 | 121154742 | ||
chr9:121161932
|
G | A | 1 | a0004c0026 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.5166G>A | p.Arg1722Arg | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 33/44 | 5483/7719 | 5166/6978 | 1722/2325 | chr9 | 121161932 | ||
chr9:121167492
|
C | T | 3 | a0003c0003a0011c0013a0017c0018 | 71 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(68): Show |
synonymous_variant | LOW | c.5659C>T | p.Leu1887Leu | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 37/44 | 5976/7719 | 5659/6978 | 1887/2325 | chr9 | 121167492 | ||
chr9:121171488
|
C | G | 1 | a0002c0023 | 1 | NA18943.hp2 | synonymous_variant | LOW | c.6357C>G | p.Ala2119Ala | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/44 | 6674/7719 | 6357/6978 | 2119/2325 | chr9 | 121171488 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:121177272
|
T | A | 1 | a0002c0002t0004 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*86T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 44/44 | 86 | chr9 | 121177272 | |||||
chr9:121177407
|
CAT | C | 1 | a0001c0001t0003 | 8 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*222_*223delAT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 44/44 | 222 | chr9 | 121177407 | |||||
chr9:121177449
|
T | TA | 6 | a0002c0002t0002a0003c0004t0002a0003c0019t0002others(3): Show | 21 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*272dupA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 44/44 | 273 | INFO_REALIGN_3_PRIME | chr9 | 121177449 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:121075293
|
G | A | 1 | a0019c0016t0002g0021 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-205+226G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121075293 | ||||||
chr9:121075444
|
G | A | 1 | a0002c0002t0001g0022 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-205+377G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121075444 | ||||||
chr9:121075483
|
C | T | 1 | a0002c0002t0001g0306 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-205+416C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121075483 | ||||||
chr9:121075488
|
T | C | 11 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0025others(8): Show | 11 | HG01109.hp2 HG01891.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-205+421T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121075488 | ||||||
chr9:121075624
|
G | A | 107 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(104): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.-205+557G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121075624 | ||||||
chr9:121076006
|
A | T | 1 | a0002c0002t0001g0121 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-205+939A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121076006 | ||||||
chr9:121076279
|
A | G | 1 | a0002c0002t0001g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-205+1212A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121076279 | ||||||
chr9:121076860
|
A | G | 66 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(63): Show | 71 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.-205+1793A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121076860 | ||||||
chr9:121076862
|
T | C | 1 | a0002c0002t0001g0034 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-205+1795T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121076862 | ||||||
chr9:121076874
|
G | A | 196 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(193): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-205+1807G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121076874 | ||||||
chr9:121076879
|
G | C | 196 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(193): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-205+1812G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121076879 | ||||||
chr9:121077005
|
G | A | 1 | a0003c0004t0001g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-205+1938G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121077005 | ||||||
chr9:121077496
|
C | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-205+2429C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121077496 | ||||||
chr9:121077521
|
C | A | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-205+2454C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121077521 | ||||||
chr9:121077537
|
G | A | 4 | a0003c0003t0001g0250a0003c0003t0001g0251a0011c0013t0001g0248others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-205+2470G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121077537 | ||||||
chr9:121077715
|
C | G | 92 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(89): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-204-2591C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121077715 | ||||||
chr9:121077715
|
CAGGAGGA others(129): Show |
C | 66 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(63): Show | 71 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.-204-2567_-204-243 others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 121077715 | |||||
chr9:121077775
|
C | G | 6 | a0003c0004t0001g0122a0003c0004t0002g0141a0003c0004t0002g0145others(3): Show | 6 | HG02486.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-204-2531C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121077775 | ||||||
chr9:121077855
|
A | G | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01261.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-204-2451A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121077855 | ||||||
chr9:121077983
|
T | C | 2 | a0002c0002t0001g0005a0002c0002t0001g0035 | 3 | HG01123.hp1 HG01361.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.-204-2323T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121077983 | ||||||
chr9:121078223
|
A | G | 8 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-204-2083A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121078223 | ||||||
chr9:121078668
|
T | G | 13 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0025others(10): Show | 13 | HG01109.hp2 HG01891.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-204-1638T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121078668 | ||||||
chr9:121078837
|
A | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-204-1469A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121078837 | ||||||
chr9:121079271
|
A | G | 6 | a0002c0002t0001g0008a0002c0002t0001g0112a0002c0002t0001g0113others(3): Show | 7 | HG00408.hp1 NA18959.hp2 NA19006.hp1 others(4): Show |
intron_variant | MODIFIER | c.-204-1035A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121079271 | ||||||
chr9:121079348
|
A | C | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-204-958A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121079348 | ||||||
chr9:121079366
|
A | G | 6 | a0002c0002t0001g0008a0002c0002t0001g0112a0002c0002t0001g0113others(3): Show | 7 | HG00408.hp1 NA18959.hp2 NA19006.hp1 others(4): Show |
intron_variant | MODIFIER | c.-204-940A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121079366 | ||||||
chr9:121079564
|
T | C | 1 | a0001c0001t0001g0194 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-204-742T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121079564 | ||||||
chr9:121079712
|
A | G | 1 | a0002c0002t0001g0110 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-204-594A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121079712 | ||||||
chr9:121079794
|
T | A | 190 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(187): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-204-512T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121079794 | ||||||
chr9:121079860
|
A | AT | 11 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0025others(8): Show | 11 | HG01109.hp2 HG01891.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-204-438dupT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 121079860 | |||||
chr9:121079908
|
G | C | 2 | a0002c0006t0001g0023a0002c0006t0001g0024 | 2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-204-398G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | chr9 | 121079908 | ||||||
chr9:121080225
|
AGTT | A | 103 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(100): Show | 108 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.-204-75_-204-73del others(3): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 1/43 | INFO_REALIGN_3_PRIME | chr9 | 121080225 | |||||
chr9:121080595
|
A | G | 247 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(244): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.-32+117A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121080595 | ||||||
chr9:121080737
|
T | C | 1 | a0002c0002t0001g0036 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-32+259T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121080737 | ||||||
chr9:121080859
|
T | C | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-32+381T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121080859 | ||||||
chr9:121080889
|
C | T | 191 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(188): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.-32+411C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121080889 | ||||||
chr9:121080992
|
T | G | 1 | a0001c0001t0001g0147 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-32+514T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121080992 | ||||||
chr9:121081035
|
A | G | 1 | a0003c0003t0001g0020 | 2 | HG01123.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-32+557A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121081035 | ||||||
chr9:121081530
|
G | C | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32+1052G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121081530 | ||||||
chr9:121081687
|
G | A | 72 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(69): Show | 77 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.-32+1209G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121081687 | ||||||
chr9:121081818
|
G | A | 104 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(101): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.-32+1340G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121081818 | ||||||
chr9:121081948
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-32+1470C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121081948 | ||||||
chr9:121081993
|
C | T | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-32+1515C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121081993 | ||||||
chr9:121082411
|
T | G | 1 | a0002c0002t0001g0037 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-32+1933T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121082411 | ||||||
chr9:121082567
|
C | A | 15 | a0003c0004t0001g0140a0003c0004t0002g0009a0003c0004t0002g0123others(12): Show | 16 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.-32+2089C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121082567 | ||||||
chr9:121082656
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-32+2178T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121082656 | ||||||
chr9:121082744
|
C | T | 1 | a0002c0002t0001g0109 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-32+2266C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121082744 | ||||||
chr9:121082768
|
G | A | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32+2290G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121082768 | ||||||
chr9:121082918
|
C | T | 2 | a0003c0003t0001g0019a0003c0003t0001g0305 | 3 | NA18967.hp2 NA18982.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-32+2440C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121082918 | ||||||
chr9:121082929
|
C | G | 1 | a0002c0002t0001g0108 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-32+2451C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121082929 | ||||||
chr9:121082969
|
C | CA | 17 | a0001c0001t0001g0011a0001c0001t0001g0196a0001c0001t0001g0197others(14): Show | 19 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.-32+2508dupA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 121082969 | |||||
chr9:121082969
|
C | CAA | 96 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(93): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.-32+2507_-32+2508d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 121082969 | |||||
chr9:121082969
|
C | CAAA | 78 | a0002c0002t0001g0038a0002c0002t0001g0040a0002c0002t0001g0041others(75): Show | 83 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(80): Show |
intron_variant | MODIFIER | c.-32+2506_-32+2508d others(5): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 121082969 | |||||
chr9:121082994
|
A | G | 247 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(244): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.-32+2516A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121082994 | ||||||
chr9:121083415
|
G | A | 191 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(188): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.-32+2937G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121083415 | ||||||
chr9:121083475
|
A | G | 1 | a0003c0003t0001g0301 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-32+2997A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121083475 | ||||||
chr9:121083546
|
G | C | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-32+3068G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121083546 | ||||||
chr9:121083571
|
G | A | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-32+3093G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121083571 | ||||||
chr9:121083831
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-32+3353G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121083831 | ||||||
chr9:121083879
|
C | T | 1 | a0025c0027t0001g0193 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-32+3401C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121083879 | ||||||
chr9:121083921
|
T | C | 13 | a0003c0004t0002g0009a0003c0004t0002g0124a0003c0004t0002g0125others(10): Show | 14 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-32+3443T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121083921 | ||||||
chr9:121083927
|
G | A | 1 | a0003c0003t0001g0252 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-32+3449G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121083927 | ||||||
chr9:121084009
|
G | A | 2 | a0003c0004t0002g0141a0003c0004t0002g0145 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-32+3531G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121084009 | ||||||
chr9:121084167
|
A | T | 1 | a0001c0001t0001g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-32+3689A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121084167 | ||||||
chr9:121084182
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-32+3704C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121084182 | ||||||
chr9:121084226
|
T | C | 23 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(20): Show | 25 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.-32+3748T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121084226 | ||||||
chr9:121084305
|
A | G | 92 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(89): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-32+3827A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121084305 | ||||||
chr9:121084342
|
A | G | 247 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(244): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.-32+3864A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121084342 | ||||||
chr9:121084504
|
G | A | 1 | a0003c0003t0001g0253 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-31-3792G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121084504 | ||||||
chr9:121084546
|
A | AT | 142 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0191others(139): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.-31-3736dupT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 121084546 | |||||
chr9:121084546
|
A | ATT | 105 | a0001c0001t0001g0216a0002c0002t0001g0001a0002c0002t0001g0005others(102): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.-31-3737_-31-3736d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 121084546 | |||||
chr9:121084676
|
C | T | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | HG00438.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-31-3620C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121084676 | ||||||
chr9:121084761
|
G | C | 13 | a0003c0004t0002g0009a0003c0004t0002g0124a0003c0004t0002g0125others(10): Show | 14 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-31-3535G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121084761 | ||||||
chr9:121085096
|
A | G | 1 | a0002c0002t0001g0107 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-31-3200A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121085096 | ||||||
chr9:121085355
|
T | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0048 | 2 | NA19003.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-31-2941T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121085355 | ||||||
chr9:121085501
|
A | G | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31-2795A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121085501 | ||||||
chr9:121085503
|
A | G | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-31-2793A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121085503 | ||||||
chr9:121085571
|
T | C | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-31-2725T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121085571 | ||||||
chr9:121085682
|
C | T | 3 | a0002c0002t0001g0104a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG00280.hp2 HG00741.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-31-2614C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121085682 | ||||||
chr9:121085880
|
A | G | 3 | a0002c0002t0001g0104a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG00280.hp2 HG00741.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-31-2416A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121085880 | ||||||
chr9:121085947
|
A | G | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-31-2349A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121085947 | ||||||
chr9:121086114
|
A | C | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31-2182A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121086114 | ||||||
chr9:121086215
|
A | G | 1 | a0003c0003t0001g0299 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-31-2081A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121086215 | ||||||
chr9:121086254
|
C | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-31-2042C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121086254 | ||||||
chr9:121086325
|
T | C | 2 | a0002c0006t0001g0025a0002c0006t0001g0026 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-31-1971T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121086325 | ||||||
chr9:121086509
|
T | C | 1 | a0012c0025t0001g0111 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-31-1787T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121086509 | ||||||
chr9:121086558
|
C | T | 104 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(101): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.-31-1738C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121086558 | ||||||
chr9:121086559
|
A | G | 288 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(285): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.-31-1737A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121086559 | ||||||
chr9:121086633
|
C | CT | 22 | a0001c0001t0001g0194a0001c0001t0001g0198a0001c0001t0001g0199others(19): Show | 22 | HG00621.hp1 HG00738.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-31-1641dupT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 121086633 | |||||
chr9:121086633
|
C | CTT | 39 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0195others(36): Show | 41 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.-31-1642_-31-1641d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 121086633 | |||||
chr9:121086633
|
C | CTTT | 6 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0237others(3): Show | 6 | HG02572.hp2 HG02970.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31-1643_-31-1641d others(5): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | INFO_REALIGN_3_PRIME | chr9 | 121086633 | |||||
chr9:121086704
|
G | A | 1 | a0002c0002t0001g0049 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-31-1592G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121086704 | ||||||
chr9:121086878
|
C | T | 1 | a0004c0026t0001g0135 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-31-1418C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121086878 | ||||||
chr9:121086919
|
C | T | 1 | a0003c0003t0001g0296 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-31-1377C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121086919 | ||||||
chr9:121086992
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-31-1304T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121086992 | ||||||
chr9:121087053
|
T | C | 1 | a0002c0002t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-31-1243T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121087053 | ||||||
chr9:121087291
|
G | A | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-31-1005G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121087291 | ||||||
chr9:121087325
|
A | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-31-971A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121087325 | ||||||
chr9:121087347
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-31-949G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121087347 | ||||||
chr9:121087584
|
G | A | 191 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(188): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.-31-712G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121087584 | ||||||
chr9:121087587
|
A | C | 1 | a0002c0002t0001g0100 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-31-709A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121087587 | ||||||
chr9:121087639
|
C | T | 9 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31-657C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121087639 | ||||||
chr9:121087646
|
G | A | 14 | a0003c0003t0001g0254a0003c0004t0002g0009a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31-650G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121087646 | ||||||
chr9:121087883
|
C | A | 1 | a0002c0006t0001g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-31-413C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121087883 | ||||||
chr9:121087894
|
C | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-31-402C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121087894 | ||||||
chr9:121087940
|
G | A | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-31-356G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121087940 | ||||||
chr9:121088178
|
G | A | 1 | a0002c0002t0001g0050 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-31-118G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 2/43 | chr9 | 121088178 | ||||||
chr9:121088962
|
A | G | 4 | a0001c0001t0001g0197a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG02630.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+419A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/43 | chr9 | 121088962 | ||||||
chr9:121088977
|
A | C | 1 | a0003c0003t0001g0254 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.217+434A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/43 | chr9 | 121088977 | ||||||
chr9:121089293
|
A | G | 1 | a0002c0002t0001g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.217+750A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/43 | chr9 | 121089293 | ||||||
chr9:121089358
|
G | A | 1 | a0002c0002t0001g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.217+815G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/43 | chr9 | 121089358 | ||||||
chr9:121089454
|
T | A | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.218-821T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/43 | chr9 | 121089454 | ||||||
chr9:121089500
|
A | G | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.218-775A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/43 | chr9 | 121089500 | ||||||
chr9:121089518
|
T | C | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.218-757T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/43 | chr9 | 121089518 | ||||||
chr9:121089568
|
T | C | 1 | a0006c0010t0001g0052 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.218-707T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/43 | chr9 | 121089568 | ||||||
chr9:121089658
|
G | A | 2 | a0003c0003t0001g0255a0003c0003t0001g0256 | 2 | NA18939.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.218-617G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/43 | chr9 | 121089658 | ||||||
chr9:121089956
|
C | T | 1 | a0007c0011t0001g0014 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.218-319C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/43 | chr9 | 121089956 | ||||||
chr9:121089998
|
G | A | 105 | a0001c0001t0001g0164a0002c0002t0001g0001a0002c0002t0001g0005others(102): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.218-277G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/43 | chr9 | 121089998 | ||||||
chr9:121090037
|
ATTATAGT others(133): Show |
A | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.218-234_218-95del | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 3/43 | INFO_REALIGN_3_PRIME | chr9 | 121090037 | |||||
chr9:121090477
|
A | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.348+72A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121090477 | ||||||
chr9:121090581
|
C | T | 182 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(179): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.348+176C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121090581 | ||||||
chr9:121090603
|
C | G | 1 | a0002c0006t0001g0033 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.348+198C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121090603 | ||||||
chr9:121090772
|
G | A | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.348+367G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121090772 | ||||||
chr9:121090922
|
G | C | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.348+517G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121090922 | ||||||
chr9:121091079
|
A | G | 197 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(194): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.348+674A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121091079 | ||||||
chr9:121091082
|
A | G | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+677A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121091082 | ||||||
chr9:121091341
|
A | G | 1 | a0002c0002t0001g0107 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.348+936A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121091341 | ||||||
chr9:121091609
|
G | A | 1 | a0003c0003t0001g0300 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.348+1204G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121091609 | ||||||
chr9:121091713
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0150 | 3 | HG02970.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.348+1308G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121091713 | ||||||
chr9:121091800
|
C | T | 2 | a0002c0002t0001g0005a0002c0002t0001g0035 | 3 | HG01123.hp1 HG01361.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.348+1395C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121091800 | ||||||
chr9:121091884
|
CT | C | 170 | a0001c0001t0001g0011a0001c0001t0001g0147a0001c0001t0001g0149others(167): Show | 181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.348+1501delT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121091884 | |||||
chr9:121091884
|
CTT | C | 17 | a0001c0001t0001g0165a0001c0001t0001g0233a0001c0001t0003g0239others(14): Show | 17 | HG01074.hp1 HG01109.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.348+1500_348+1501d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121091884 | |||||
chr9:121091936
|
C | T | 1 | a0003c0003t0001g0295 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.348+1531C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121091936 | ||||||
chr9:121091986
|
G | A | 3 | a0010c0014t0001g0167a0010c0014t0001g0169a0020c0034t0001g0168 | 3 | HG02809.hp2 HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.348+1581G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121091986 | ||||||
chr9:121091987
|
C | T | 73 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(70): Show | 78 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.348+1582C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121091987 | ||||||
chr9:121092124
|
C | G | 50 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(47): Show | 52 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.348+1719C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092124 | ||||||
chr9:121092151
|
C | G | 50 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(47): Show | 52 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.348+1746C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092151 | ||||||
chr9:121092357
|
G | A | 1 | a0004c0026t0001g0135 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.348+1952G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092357 | ||||||
chr9:121092427
|
T | TATAG | 190 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(187): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.348+2038_348+2041d others(6): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092427 | |||||
chr9:121092443
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.348+2038G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092443 | ||||||
chr9:121092443
|
GATAATAT others(105): Show |
G | 2 | a0002c0006t0001g0025a0002c0006t0001g0026 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.348+2042_348+2153d others(2): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092443 | |||||
chr9:121092457
|
ATATATAT others(88): Show |
A | 16 | a0001c0001t0001g0149a0001c0001t0001g0186a0001c0001t0001g0187others(13): Show | 19 | HG00280.hp1 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.348+2119_348+2213d others(97): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092457 | |||||
chr9:121092457
|
ATATATAT others(107): Show |
A | 1 | a0001c0001t0001g0151 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.348+2100_348+2213d others(2): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092457 | |||||
chr9:121092459
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.348+2054A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092459 | ||||||
chr9:121092460
|
T | C | 2 | a0003c0004t0002g0141a0003c0004t0002g0145 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.348+2055T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092460 | ||||||
chr9:121092464
|
TATA | T | 12 | a0003c0004t0002g0009a0003c0004t0002g0125a0003c0004t0002g0128others(9): Show | 13 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.348+2063_348+2065d others(5): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092464 | |||||
chr9:121092467
|
AATATATA others(69): Show |
A | 32 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0147others(29): Show | 37 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.348+2175_349-2233d others(78): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092467 | |||||
chr9:121092474
|
A | C | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.348+2069A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092474 | ||||||
chr9:121092476
|
C | A | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.348+2071C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092476 | ||||||
chr9:121092478
|
A | ATATATAA others(9): Show |
1 | a0001c0001t0001g0199 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.348+2079_348+2080i others(18): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092478 | |||||
chr9:121092478
|
A | ATATATAT others(10): Show |
22 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(19): Show | 24 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.348+2082_348+2098d others(19): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092478 | |||||
chr9:121092485
|
T | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01261.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.348+2080T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092485 | ||||||
chr9:121092491
|
A | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.348+2086A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092491 | ||||||
chr9:121092495
|
CTA | C | 120 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0213others(117): Show | 127 | HG00140.hp2 HG00438.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.348+2099_348+2100d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092495 | |||||
chr9:121092500
|
T | C | 1 | a0002c0002t0001g0100 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.348+2095T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092500 | ||||||
chr9:121092504
|
T | A | 86 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(83): Show | 90 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.348+2099T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092504 | ||||||
chr9:121092505
|
A | T | 87 | a0001c0001t0001g0011a0002c0002t0001g0001a0002c0002t0001g0005others(84): Show | 92 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.348+2100A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092505 | ||||||
chr9:121092512
|
A | C | 86 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(83): Show | 90 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.348+2107A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092512 | ||||||
chr9:121092514
|
C | A | 86 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(83): Show | 90 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.348+2109C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092514 | ||||||
chr9:121092514
|
C | CTA | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG02109.hp1 HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.348+2118_348+2119d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092514 | |||||
chr9:121092516
|
ATATATAT others(10): Show |
A | 1 | a0002c0002t0001g0097 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.348+2120_348+2136d others(19): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092516 | |||||
chr9:121092516
|
ATATATAT others(160): Show |
A | 4 | a0002c0002t0001g0007a0002c0002t0001g0050a0002c0002t0001g0108others(1): Show | 5 | HG00621.hp2 HG02071.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+2120_349-2197d others(2): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092516 | |||||
chr9:121092522
|
A | G | 89 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(86): Show | 94 | HG00140.hp2 HG00597.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.348+2117A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092522 | ||||||
chr9:121092524
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.348+2119A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092524 | ||||||
chr9:121092524
|
AATATATA others(12): Show |
A | 1 | a0001c0001t0001g0228 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.348+2138_348+2156d others(21): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092524 | |||||
chr9:121092531
|
A | C | 1 | a0001c0001t0001g0222 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.348+2126A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092531 | ||||||
chr9:121092533
|
C | A | 1 | a0001c0001t0001g0222 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.348+2128C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092533 | ||||||
chr9:121092533
|
C | CTA | 86 | a0001c0001t0001g0218a0001c0001t0001g0229a0001c0001t0001g0230others(83): Show | 91 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(88): Show |
intron_variant | MODIFIER | c.348+2136_348+2137d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092533 | |||||
chr9:121092535
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.348+2137_348+2138i others(21): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092535 | |||||
chr9:121092535
|
ATATATAT others(10): Show |
A | 3 | a0004c0007t0001g0010a0004c0007t0001g0137a0004c0007t0001g0138 | 4 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+2138_348+2154d others(19): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092535 | |||||
chr9:121092535
|
ATATATAT others(29): Show |
A | 2 | a0004c0007t0001g0136a0004c0007t0001g0139 | 2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.348+2138_348+2173d others(38): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092535 | |||||
chr9:121092535
|
ATATATAT others(105): Show |
A | 1 | a0001c0001t0001g0011 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.348+2138_349-2234d others(2): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092535 | |||||
chr9:121092535
|
ATATATAT others(141): Show |
A | 1 | a0003c0003t0001g0295 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.348+2138_349-2198d others(2): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092535 | |||||
chr9:121092541
|
A | G | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.348+2136A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092541 | ||||||
chr9:121092541
|
ATT | A | 12 | a0001c0001t0001g0197a0001c0001t0001g0214a0001c0001t0001g0234others(9): Show | 12 | HG00438.hp2 HG01109.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.348+2137_348+2138d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092541 | ||||||
chr9:121092543
|
T | A | 224 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0189others(221): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.348+2138T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092543 | ||||||
chr9:121092543
|
T | C | 3 | a0002c0002t0001g0104a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG00280.hp2 HG00741.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.348+2138T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092543 | ||||||
chr9:121092543
|
T | G | 2 | a0002c0002t0001g0045a0002c0002t0001g0120 | 2 | NA18946.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.348+2138T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092543 | ||||||
chr9:121092554
|
ATATATAT others(86): Show |
A | 1 | a0001c0001t0001g0189 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.348+2214_349-2177d others(95): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092554 | |||||
chr9:121092554
|
ATATATAT others(181): Show |
A | 2 | a0002c0002t0001g0045a0002c0002t0001g0120 | 2 | NA18946.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.348+2176_349-2120d others(2): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092554 | |||||
chr9:121092556
|
A | ATC | 13 | a0003c0004t0002g0009a0003c0004t0002g0124a0003c0004t0002g0125others(10): Show | 14 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.348+2152_348+2153i others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092556 | |||||
chr9:121092559
|
T | G | 2 | a0002c0006t0001g0025a0002c0006t0001g0026 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.348+2154T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092559 | ||||||
chr9:121092562
|
A | G | 100 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(97): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.348+2157A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092562 | ||||||
chr9:121092562
|
A | T | 2 | a0001c0001t0001g0213a0004c0026t0001g0135 | 2 | HG03486.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.348+2157A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092562 | ||||||
chr9:121092571
|
C | CTA | 3 | a0001c0001t0001g0197a0001c0001t0001g0234a0004c0026t0001g0135 | 3 | HG02630.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.348+2175_348+2176d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092571 | |||||
chr9:121092571
|
CTA | C | 3 | a0001c0001t0003g0238a0001c0001t0003g0242a0026c0033t0001g0170 | 3 | HG00438.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.348+2175_348+2176d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092571 | |||||
chr9:121092571
|
CTATATAT others(52): Show |
C | 1 | a0010c0014t0001g0167 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.348+2175_348+2233d others(61): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092571 | |||||
chr9:121092573
|
ATATATAT others(48): Show |
A | 1 | a0021c0030t0001g0235 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.348+2177_348+2231d others(57): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092573 | |||||
chr9:121092573
|
ATATATAT others(162): Show |
A | 86 | a0001c0001t0001g0213a0002c0002t0001g0001a0002c0002t0001g0005others(83): Show | 90 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.348+2195_349-2120d others(2): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092573 | |||||
chr9:121092575
|
ATATATAA others(65): Show |
A | 6 | a0001c0001t0003g0239a0001c0001t0003g0240a0001c0001t0003g0241others(3): Show | 6 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+2177_349-2235d others(74): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092575 | |||||
chr9:121092579
|
A | G | 77 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(74): Show | 82 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.348+2174A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092579 | ||||||
chr9:121092581
|
A | G | 103 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(100): Show | 109 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.348+2176A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092581 | ||||||
chr9:121092581
|
A | T | 3 | a0004c0007t0001g0010a0004c0007t0001g0137a0004c0007t0001g0138 | 4 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+2176A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092581 | ||||||
chr9:121092590
|
C | CTA | 4 | a0003c0004t0002g0123a0004c0007t0001g0010a0004c0007t0001g0137others(1): Show | 5 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.348+2194_348+2195d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092590 | |||||
chr9:121092592
|
ATATATAT others(48): Show |
A | 2 | a0001c0001t0001g0214a0026c0033t0001g0170 | 2 | HG00438.hp1 HG00438.hp2 |
intron_variant | MODIFIER | c.348+2214_349-2215d others(57): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092592 | |||||
chr9:121092592
|
ATATATAT others(143): Show |
A | 78 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(75): Show | 83 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.348+2230_349-2104d others(2): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092592 | |||||
chr9:121092600
|
A | G | 14 | a0003c0004t0002g0009a0003c0004t0002g0124a0003c0004t0002g0125others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.348+2195A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092600 | ||||||
chr9:121092600
|
A | T | 3 | a0001c0005t0001g0015a0004c0007t0001g0136a0004c0007t0001g0139 | 4 | HG02895.hp1 HG03225.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+2195A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092600 | ||||||
chr9:121092611
|
ATATATAT others(124): Show |
A | 12 | a0003c0004t0002g0009a0003c0004t0002g0124a0003c0004t0002g0125others(9): Show | 13 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.348+2214_349-2139d others(2): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092611 | |||||
chr9:121092613
|
ATATATTA others(27): Show |
A | 2 | a0001c0001t0003g0238a0001c0001t0003g0242 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.348+2214_349-2236d others(36): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092613 | |||||
chr9:121092619
|
T | A | 13 | a0001c0001t0001g0197a0001c0001t0001g0218a0001c0001t0001g0222others(10): Show | 14 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.348+2214T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092619 | ||||||
chr9:121092619
|
T | G | 11 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0027others(8): Show | 11 | HG01891.hp1 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.348+2214T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092619 | ||||||
chr9:121092619
|
TATATATA others(124): Show |
T | 1 | a0001c0001t0001g0016 | 2 | NA18986.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.348+2233_349-2120d others(2): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092619 | |||||
chr9:121092620
|
A | T | 1 | a0004c0007t0001g0139 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.348+2215A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092620 | ||||||
chr9:121092621
|
T | A | 1 | a0004c0007t0001g0139 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.348+2216T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092621 | ||||||
chr9:121092630
|
ATATATAT others(105): Show |
A | 39 | a0001c0001t0001g0017a0001c0001t0001g0195a0001c0001t0001g0196others(36): Show | 40 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.349-2232_349-2121d others(2): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092630 | |||||
chr9:121092635
|
T | G | 1 | a0002c0002t0001g0097 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.348+2230T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092635 | ||||||
chr9:121092636
|
A | G | 2 | a0002c0006t0001g0025a0002c0006t0001g0026 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.348+2231A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092636 | ||||||
chr9:121092636
|
ATAATATA others(99): Show |
A | 1 | a0002c0002t0001g0097 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.348+2234_349-2144d others(2): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092636 | |||||
chr9:121092638
|
A | G | 2 | a0003c0004t0002g0123a0003c0004t0002g0131 | 2 | HG03579.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.348+2233A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092638 | ||||||
chr9:121092638
|
A | T | 4 | a0001c0001t0001g0194a0001c0001t0001g0222a0001c0001t0001g0233others(1): Show | 4 | HG02559.hp1 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+2233A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092638 | ||||||
chr9:121092642
|
T | C | 1 | a0004c0007t0001g0010 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.348+2237T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092642 | ||||||
chr9:121092647
|
C | CTA | 9 | a0001c0001t0001g0197a0001c0001t0001g0234a0004c0007t0001g0010others(6): Show | 10 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.349-2234_349-2233d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092647 | |||||
chr9:121092647
|
C | CTATATAT others(12): Show |
1 | a0010c0014t0001g0167 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.349-2175_349-2157d others(21): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092647 | |||||
chr9:121092649
|
ATATATAA others(86): Show |
A | 3 | a0001c0001t0001g0194a0003c0004t0002g0123a0003c0004t0002g0131 | 3 | HG03579.hp1 NA18948.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.349-2232_349-2140d others(95): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092649 | |||||
chr9:121092653
|
A | C | 8 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-2235A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092653 | ||||||
chr9:121092655
|
A | ATT | 4 | a0001c0001t0001g0218a0001c0001t0001g0222a0001c0001t0001g0233others(1): Show | 4 | HG02559.hp1 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-2233_349-2232i others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092655 | ||||||
chr9:121092666
|
ATATATAT others(69): Show |
A | 3 | a0001c0001t0001g0218a0002c0006t0001g0023a0002c0006t0001g0024 | 3 | HG01891.hp1 HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.349-2195_349-2120d others(78): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092666 | |||||
chr9:121092674
|
A | T | 5 | a0001c0001t0001g0197a0001c0001t0001g0222a0001c0001t0001g0233others(2): Show | 5 | HG02559.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-2214A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092674 | ||||||
chr9:121092683
|
C | A | 1 | a0001c0001t0003g0239 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.349-2205C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092683 | ||||||
chr9:121092685
|
ATATATAT others(50): Show |
A | 3 | a0001c0001t0001g0222a0001c0001t0001g0233a0001c0001t0001g0236 | 3 | HG02559.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.349-2176_349-2120d others(59): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092685 | |||||
chr9:121092693
|
A | G | 2 | a0002c0006t0001g0025a0002c0006t0001g0026 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.349-2195A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092693 | ||||||
chr9:121092693
|
A | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0234 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.349-2195A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092693 | ||||||
chr9:121092702
|
CTA | C | 1 | a0001c0005t0001g0003 | 3 | HG01070.hp2 HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.349-2177_349-2176d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092702 | |||||
chr9:121092712
|
A | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0234 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.349-2176A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092712 | ||||||
chr9:121092721
|
CTA | C | 13 | a0001c0001t0001g0214a0001c0001t0003g0238a0001c0001t0003g0239others(10): Show | 13 | HG00438.hp2 HG01109.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.349-2156_349-2155d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092721 | |||||
chr9:121092723
|
ATATATAT others(12): Show |
A | 2 | a0001c0001t0001g0197a0001c0001t0001g0234 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.349-2156_349-2138d others(21): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092723 | |||||
chr9:121092728
|
TA | T | 4 | a0002c0002t0001g0007a0002c0002t0001g0050a0002c0002t0001g0108others(1): Show | 5 | HG00621.hp2 HG02071.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-2159delA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092728 | ||||||
chr9:121092730
|
T | G | 4 | a0002c0002t0001g0007a0002c0002t0001g0050a0002c0002t0001g0108others(1): Show | 5 | HG00621.hp2 HG02071.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-2158T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092730 | ||||||
chr9:121092731
|
A | G | 3 | a0002c0006t0001g0025a0002c0006t0001g0026a0003c0003t0001g0295 | 3 | HG01109.hp2 HG03831.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.349-2157A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092731 | ||||||
chr9:121092732
|
T | A | 2 | a0002c0006t0001g0025a0002c0006t0001g0026 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.349-2156T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092732 | ||||||
chr9:121092732
|
TA | T | 4 | a0002c0002t0001g0007a0002c0002t0001g0050a0002c0002t0001g0108others(1): Show | 5 | HG00621.hp2 HG02071.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-2154delA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092732 | |||||
chr9:121092733
|
A | G | 1 | a0003c0003t0001g0295 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.349-2155A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092733 | ||||||
chr9:121092733
|
A | T | 12 | a0001c0001t0001g0214a0001c0001t0003g0238a0001c0001t0003g0239others(9): Show | 12 | HG00438.hp2 HG01109.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.349-2155A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092733 | ||||||
chr9:121092740
|
A | C | 6 | a0002c0002t0001g0007a0002c0002t0001g0050a0002c0002t0001g0108others(3): Show | 7 | HG00621.hp2 HG01109.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-2148A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092740 | ||||||
chr9:121092742
|
C | A | 6 | a0002c0002t0001g0007a0002c0002t0001g0050a0002c0002t0001g0108others(3): Show | 7 | HG00621.hp2 HG01109.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-2146C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092742 | ||||||
chr9:121092742
|
C | CTA | 8 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0175others(5): Show | 8 | HG01496.hp2 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.349-2139_349-2138d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092742 | |||||
chr9:121092749
|
T | A | 1 | a0002c0002t0001g0097 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.349-2139T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092749 | ||||||
chr9:121092750
|
A | ATT | 10 | a0001c0001t0001g0214a0001c0001t0003g0238a0001c0001t0003g0239others(7): Show | 10 | HG00438.hp2 HG01109.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.349-2138_349-2137i others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092750 | ||||||
chr9:121092750
|
A | G | 2 | a0002c0002t0001g0045a0002c0002t0001g0098 | 2 | HG01081.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.349-2138A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092750 | ||||||
chr9:121092750
|
A | T | 40 | a0001c0001t0001g0017a0001c0001t0001g0194a0001c0001t0001g0195others(37): Show | 41 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.349-2138A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092750 | ||||||
chr9:121092769
|
T | G | 19 | a0002c0002t0001g0040a0002c0002t0001g0112a0002c0006t0001g0023others(16): Show | 20 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.349-2119T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092769 | ||||||
chr9:121092790
|
G | A | 247 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(244): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.349-2098G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092790 | ||||||
chr9:121092816
|
TA | T | 12 | a0001c0001t0001g0165a0001c0001t0001g0180a0001c0001t0001g0192others(9): Show | 12 | HG00140.hp1 HG01261.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.349-2071delA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092816 | ||||||
chr9:121092817
|
AT | A | 283 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(280): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.349-2058delT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121092817 | |||||
chr9:121092819
|
T | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0153a0002c0002t0001g0056others(1): Show | 6 | HG00639.hp1 HG00735.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.349-2069T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092819 | ||||||
chr9:121092820
|
T | A | 106 | a0001c0001t0001g0012a0001c0001t0001g0150a0001c0001t0001g0164others(103): Show | 114 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.349-2068T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092820 | ||||||
chr9:121092822
|
T | A | 5 | a0003c0003t0001g0018a0003c0003t0001g0264a0003c0003t0001g0265others(2): Show | 6 | HG02976.hp1 HG03490.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-2066T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092822 | ||||||
chr9:121092889
|
A | G | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(246): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.349-1999A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092889 | ||||||
chr9:121092907
|
A | G | 199 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(196): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.349-1981A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092907 | ||||||
chr9:121092963
|
C | T | 1 | a0008c0012t0002g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.349-1925C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092963 | ||||||
chr9:121092989
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.349-1899A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121092989 | ||||||
chr9:121093050
|
C | G | 306 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0012others(303): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.349-1838C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121093050 | ||||||
chr9:121093052
|
C | T | 12 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0025others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.349-1836C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121093052 | ||||||
chr9:121093096
|
C | T | 3 | a0002c0002t0001g0095a0002c0002t0001g0096a0002c0002t0001g0103 | 3 | HG00140.hp1 HG01261.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.349-1792C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121093096 | ||||||
chr9:121093215
|
A | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG02451.hp2 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.349-1673A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121093215 | ||||||
chr9:121093494
|
G | A | 1 | a0002c0002t0001g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.349-1394G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121093494 | ||||||
chr9:121093656
|
A | G | 9 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0027others(6): Show | 9 | HG01891.hp1 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.349-1232A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121093656 | ||||||
chr9:121094081
|
G | A | 2 | a0002c0002t0001g0057a0002c0002t0001g0097 | 2 | HG01255.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.349-807G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121094081 | ||||||
chr9:121094103
|
GTCCCCGC others(4): Show |
G | 9 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0027others(6): Show | 9 | HG01891.hp1 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.349-779_349-769del others(11): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | INFO_REALIGN_3_PRIME | chr9 | 121094103 | |||||
chr9:121094126
|
G | C | 191 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(188): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.349-762G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121094126 | ||||||
chr9:121094588
|
A | G | 1 | a0001c0005t0001g0015 | 2 | NA18971.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.349-300A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121094588 | ||||||
chr9:121094647
|
T | G | 5 | a0003c0004t0002g0125a0003c0004t0002g0130a0003c0004t0002g0131others(2): Show | 5 | HG00099.hp2 HG02027.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-241T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121094647 | ||||||
chr9:121094807
|
C | T | 104 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(101): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.349-81C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121094807 | ||||||
chr9:121094862
|
G | T | 1 | a0003c0003t0001g0301 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.349-26G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 4/43 | chr9 | 121094862 | ||||||
chr9:121095032
|
C | A | 2 | a0002c0006t0001g0027a0002c0006t0001g0028 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.479+14C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 5/43 | chr9 | 121095032 | ||||||
chr9:121095380
|
C | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.479+362C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 5/43 | chr9 | 121095380 | ||||||
chr9:121095916
|
G | T | 191 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(188): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.480-506G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 5/43 | chr9 | 121095916 | ||||||
chr9:121095995
|
G | A | 1 | a0002c0002t0001g0058 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.480-427G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 5/43 | chr9 | 121095995 | ||||||
chr9:121096046
|
C | A | 1 | a0002c0002t0001g0110 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.480-376C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 5/43 | chr9 | 121096046 | ||||||
chr9:121096152
|
T | A | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(246): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.480-270T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 5/43 | chr9 | 121096152 | ||||||
chr9:121096285
|
T | G | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.480-137T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 5/43 | chr9 | 121096285 | ||||||
chr9:121096774
|
C | T | 12 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0025others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.621+211C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 6/43 | chr9 | 121096774 | ||||||
chr9:121096968
|
G | GT | 20 | a0001c0001t0001g0179a0001c0001t0001g0236a0002c0002t0001g0093others(17): Show | 21 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.621+418dupT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr9 | 121096968 | |||||
chr9:121096972
|
T | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.621+409T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 6/43 | chr9 | 121096972 | ||||||
chr9:121097023
|
G | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0180 | 2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.621+460G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 6/43 | chr9 | 121097023 | ||||||
chr9:121097387
|
T | A | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.621+824T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 6/43 | chr9 | 121097387 | ||||||
chr9:121097583
|
G | A | 3 | a0008c0012t0002g0142a0008c0012t0002g0143a0008c0012t0002g0144 | 3 | HG02976.hp1 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.622-803G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 6/43 | chr9 | 121097583 | ||||||
chr9:121097584
|
T | TC | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(246): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.622-801dupC | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 6/43 | INFO_REALIGN_3_PRIME | chr9 | 121097584 | |||||
chr9:121097795
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.622-591C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 6/43 | chr9 | 121097795 | ||||||
chr9:121097998
|
T | G | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.622-388T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 6/43 | chr9 | 121097998 | ||||||
chr9:121098097
|
C | T | 92 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(89): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.622-289C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 6/43 | chr9 | 121098097 | ||||||
chr9:121098121
|
T | C | 1 | a0003c0004t0001g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.622-265T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 6/43 | chr9 | 121098121 | ||||||
chr9:121098156
|
A | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | NA18939.hp2 NA18974.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.622-230A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 6/43 | chr9 | 121098156 | ||||||
chr9:121098235
|
T | C | 1 | a0003c0004t0002g0132 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.622-151T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 6/43 | chr9 | 121098235 | ||||||
chr9:121098580
|
T | TAAATTTA others(322): Show |
1 | a0008c0012t0002g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.808+22_808+23insGG others(327): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr9 | 121098580 | |||||
chr9:121098734
|
C | T | 1 | a0002c0006t0001g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.808+162C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121098734 | ||||||
chr9:121098736
|
C | T | 13 | a0003c0004t0002g0009a0003c0004t0002g0124a0003c0004t0002g0125others(10): Show | 14 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.808+164C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121098736 | ||||||
chr9:121098791
|
G | A | 7 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0175others(4): Show | 7 | HG01496.hp2 HG02109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.808+219G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121098791 | ||||||
chr9:121098809
|
G | A | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.808+237G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121098809 | ||||||
chr9:121098829
|
C | CA | 16 | a0003c0003t0001g0300a0003c0004t0001g0140a0003c0004t0002g0009others(13): Show | 17 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.808+268dupA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr9 | 121098829 | |||||
chr9:121098829
|
C | CAA | 176 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(173): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.808+267_808+268dup others(2): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr9 | 121098829 | |||||
chr9:121098841
|
C | A | 2 | a0003c0004t0002g0141a0003c0004t0002g0145 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.808+269C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121098841 | ||||||
chr9:121099149
|
C | G | 1 | a0003c0003t0001g0251 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.808+577C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099149 | ||||||
chr9:121099227
|
A | G | 3 | a0002c0006t0001g0029a0002c0006t0001g0032a0013c0021t0001g0030 | 3 | HG02647.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.808+655A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099227 | ||||||
chr9:121099271
|
G | T | 1 | a0004c0026t0001g0135 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.808+699G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099271 | ||||||
chr9:121099292
|
T | C | 1 | a0002c0002t0001g0036 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.808+720T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099292 | ||||||
chr9:121099311
|
G | A | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.808+739G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099311 | ||||||
chr9:121099350
|
G | T | 8 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.808+778G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099350 | ||||||
chr9:121099545
|
A | G | 2 | a0002c0006t0001g0025a0002c0006t0001g0026 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.808+973A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099545 | ||||||
chr9:121099578
|
G | C | 104 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(101): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.808+1006G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099578 | ||||||
chr9:121099610
|
C | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.808+1038C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099610 | ||||||
chr9:121099620
|
G | A | 7 | a0001c0005t0001g0003a0001c0005t0001g0166a0001c0005t0001g0181others(4): Show | 9 | HG00280.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.808+1048G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099620 | ||||||
chr9:121099675
|
A | G | 2 | a0001c0001t0001g0211a0022c0028t0001g0212 | 2 | HG00408.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.808+1103A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099675 | ||||||
chr9:121099693
|
ACAG | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG02451.hp2 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.808+1124_808+1126d others(5): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr9 | 121099693 | |||||
chr9:121099698
|
A | C | 3 | a0001c0001t0001g0218a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG02451.hp2 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.808+1126A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099698 | ||||||
chr9:121099737
|
G | A | 3 | a0002c0002t0001g0104a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG00280.hp2 HG00741.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.808+1165G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099737 | ||||||
chr9:121099743
|
C | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG00408.hp2 HG02129.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.808+1171C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099743 | ||||||
chr9:121099773
|
A | G | 184 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(181): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.808+1201A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121099773 | ||||||
chr9:121100000
|
G | T | 1 | a0002c0023t0001g0092 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.808+1428G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121100000 | ||||||
chr9:121100077
|
C | T | 1 | a0002c0002t0001g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.808+1505C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121100077 | ||||||
chr9:121100099
|
C | T | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.808+1527C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121100099 | ||||||
chr9:121100314
|
C | A | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.808+1742C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121100314 | ||||||
chr9:121100315
|
A | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.808+1743A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121100315 | ||||||
chr9:121100381
|
C | G | 1 | a0001c0001t0001g0173 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.808+1809C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121100381 | ||||||
chr9:121100408
|
G | A | 13 | a0003c0004t0002g0009a0003c0004t0002g0124a0003c0004t0002g0125others(10): Show | 14 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.808+1836G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121100408 | ||||||
chr9:121100605
|
G | A | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(246): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.808+2033G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121100605 | ||||||
chr9:121100650
|
G | C | 72 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(69): Show | 77 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.808+2078G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121100650 | ||||||
chr9:121100807
|
CAAAG | C | 3 | a0006c0010t0001g0052a0006c0010t0001g0090a0006c0010t0001g0091 | 3 | HG01070.hp1 HG02698.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.808+2238_808+2241d others(6): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr9 | 121100807 | |||||
chr9:121101000
|
AAGAG | A | 67 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(64): Show | 72 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.808+2432_808+2435d others(6): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr9 | 121101000 | |||||
chr9:121101005
|
A | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.808+2433A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101005 | ||||||
chr9:121101085
|
A | G | 2 | a0002c0002t0001g0088a0002c0002t0001g0089 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.808+2513A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101085 | ||||||
chr9:121101210
|
C | A | 253 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(250): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.808+2638C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101210 | ||||||
chr9:121101489
|
A | G | 9 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0027others(6): Show | 9 | HG01891.hp1 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.808+2917A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101489 | ||||||
chr9:121101538
|
T | A | 182 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(179): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.808+2966T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101538 | ||||||
chr9:121101673
|
A | G | 1 | a0004c0007t0001g0139 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.808+3101A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101673 | ||||||
chr9:121101712
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.808+3140A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101712 | ||||||
chr9:121101898
|
T | G | 1 | a0001c0001t0003g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.808+3326T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101898 | ||||||
chr9:121101910
|
G | T | 1 | a0001c0001t0003g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.808+3338G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101910 | ||||||
chr9:121101916
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.808+3344G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101916 | ||||||
chr9:121101923
|
C | A | 1 | a0001c0001t0003g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.808+3351C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101923 | ||||||
chr9:121101930
|
G | C | 1 | a0001c0001t0003g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.808+3358G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101930 | ||||||
chr9:121101938
|
T | C | 1 | a0001c0001t0003g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.808+3366T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101938 | ||||||
chr9:121101943
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.808+3371C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101943 | ||||||
chr9:121101947
|
G | T | 1 | a0001c0001t0003g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.808+3375G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121101947 | ||||||
chr9:121102070
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.808+3498C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121102070 | ||||||
chr9:121102095
|
A | G | 1 | a0002c0006t0001g0033 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.808+3523A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121102095 | ||||||
chr9:121102379
|
G | T | 92 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(89): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.808+3807G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121102379 | ||||||
chr9:121102685
|
G | T | 1 | a0001c0001t0001g0214 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.808+4113G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121102685 | ||||||
chr9:121102740
|
C | A | 63 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0149others(60): Show | 65 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.808+4168C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121102740 | ||||||
chr9:121102866
|
G | T | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.808+4294G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121102866 | ||||||
chr9:121102867
|
A | T | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.808+4295A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121102867 | ||||||
chr9:121103002
|
C | T | 5 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.808+4430C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121103002 | ||||||
chr9:121103034
|
A | G | 1 | a0003c0003t0001g0298 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.808+4462A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121103034 | ||||||
chr9:121103168
|
A | C | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.808+4596A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121103168 | ||||||
chr9:121103176
|
G | A | 67 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(64): Show | 72 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.808+4604G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121103176 | ||||||
chr9:121103182
|
T | C | 4 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.808+4610T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121103182 | ||||||
chr9:121103188
|
T | C | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.809-4614T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121103188 | ||||||
chr9:121103493
|
G | A | 3 | a0002c0006t0001g0029a0002c0006t0001g0032a0013c0021t0001g0030 | 3 | HG02647.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.809-4309G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121103493 | ||||||
chr9:121103638
|
G | A | 178 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(175): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.809-4164G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121103638 | ||||||
chr9:121103702
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.809-4100A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121103702 | ||||||
chr9:121103729
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0001g0234 | 2 | HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.809-4073G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121103729 | ||||||
chr9:121103768
|
T | A | 1 | a0002c0002t0001g0055 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.809-4034T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121103768 | ||||||
chr9:121103783
|
C | T | 2 | a0002c0002t0001g0086a0002c0002t0001g0087 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.809-4019C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121103783 | ||||||
chr9:121103867
|
C | G | 106 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(103): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.809-3935C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121103867 | ||||||
chr9:121103894
|
G | A | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.809-3908G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121103894 | ||||||
chr9:121104069
|
C | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0203a0001c0001t0001g0204 | 3 | HG00621.hp1 NA19060.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.809-3733C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121104069 | ||||||
chr9:121104075
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.809-3727C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121104075 | ||||||
chr9:121104167
|
C | T | 12 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0025others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.809-3635C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121104167 | ||||||
chr9:121104222
|
G | A | 1 | a0003c0004t0001g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.809-3580G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121104222 | ||||||
chr9:121104223
|
T | C | 15 | a0003c0004t0001g0140a0003c0004t0002g0009a0003c0004t0002g0123others(12): Show | 16 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.809-3579T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121104223 | ||||||
chr9:121104285
|
A | G | 1 | a0002c0002t0001g0109 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.809-3517A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121104285 | ||||||
chr9:121104349
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.809-3453G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121104349 | ||||||
chr9:121104463
|
G | A | 9 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.809-3339G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121104463 | ||||||
chr9:121104557
|
AAAAAG | A | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.809-3235_809-3231d others(7): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr9 | 121104557 | |||||
chr9:121104694
|
A | AT | 54 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0151others(51): Show | 56 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.809-3084dupT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr9 | 121104694 | |||||
chr9:121104694
|
A | ATT | 98 | a0001c0001t0001g0195a0001c0001t0001g0208a0001c0001t0001g0217others(95): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.809-3085_809-3084d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr9 | 121104694 | |||||
chr9:121104694
|
A | ATTT | 31 | a0001c0001t0003g0243a0002c0002t0001g0034a0002c0002t0001g0040others(28): Show | 32 | HG00323.hp2 HG00408.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.809-3086_809-3084d others(5): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr9 | 121104694 | |||||
chr9:121104694
|
A | ATTTT | 41 | a0002c0002t0001g0044a0003c0003t0001g0018a0003c0003t0001g0019others(38): Show | 44 | HG00140.hp2 HG00597.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.809-3087_809-3084d others(6): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr9 | 121104694 | |||||
chr9:121104694
|
A | ATTTTT | 24 | a0003c0003t0001g0004a0003c0003t0001g0116a0003c0003t0001g0253others(21): Show | 26 | HG00741.hp1 HG01106.hp2 HG01952.hp1 others(23): Show |
intron_variant | MODIFIER | c.809-3088_809-3084d others(7): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr9 | 121104694 | |||||
chr9:121104883
|
T | C | 1 | a0002c0002t0001g0060 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.809-2919T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121104883 | ||||||
chr9:121104985
|
C | T | 1 | a0003c0003t0001g0292 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.809-2817C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121104985 | ||||||
chr9:121105046
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.809-2756T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121105046 | ||||||
chr9:121105192
|
C | G | 106 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(103): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.809-2610C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121105192 | ||||||
chr9:121105374
|
T | C | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-2428T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121105374 | ||||||
chr9:121105443
|
C | T | 1 | a0002c0023t0001g0092 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.809-2359C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121105443 | ||||||
chr9:121105504
|
T | C | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(246): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.809-2298T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121105504 | ||||||
chr9:121105630
|
G | A | 3 | a0002c0002t0001g0104a0002c0002t0001g0105a0002c0002t0001g0106 | 3 | HG00280.hp2 HG00741.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.809-2172G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121105630 | ||||||
chr9:121105703
|
A | G | 1 | a0003c0003t0001g0300 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.809-2099A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121105703 | ||||||
chr9:121105774
|
T | A | 1 | a0001c0001t0001g0175 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.809-2028T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121105774 | ||||||
chr9:121105880
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.809-1922C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121105880 | ||||||
chr9:121105913
|
T | C | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.809-1889T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121105913 | ||||||
chr9:121106071
|
G | A | 192 | a0001c0001t0001g0216a0002c0002t0001g0001a0002c0002t0001g0005others(189): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.809-1731G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121106071 | ||||||
chr9:121106212
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.809-1590G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121106212 | ||||||
chr9:121106249
|
G | T | 1 | a0002c0002t0001g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.809-1553G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121106249 | ||||||
chr9:121106275
|
G | T | 106 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(103): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.809-1527G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121106275 | ||||||
chr9:121106337
|
CA | C | 205 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(202): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.809-1447delA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | INFO_REALIGN_3_PRIME | chr9 | 121106337 | |||||
chr9:121106359
|
A | T | 9 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.809-1443A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121106359 | ||||||
chr9:121106373
|
G | A | 2 | a0002c0002t0001g0040a0002c0002t0001g0081 | 2 | HG02135.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.809-1429G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121106373 | ||||||
chr9:121106389
|
C | T | 2 | a0002c0002t0002g0114a0016c0020t0001g0115 | 2 | NA18959.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.809-1413C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121106389 | ||||||
chr9:121106800
|
A | G | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.809-1002A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121106800 | ||||||
chr9:121106978
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.809-824A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121106978 | ||||||
chr9:121106979
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.809-823G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121106979 | ||||||
chr9:121107171
|
A | G | 3 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0001t0001g0202 | 3 | NA18949.hp2 NA18950.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.809-631A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121107171 | ||||||
chr9:121107237
|
T | C | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(252): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.809-565T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121107237 | ||||||
chr9:121107479
|
T | A | 1 | a0001c0001t0001g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.809-323T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121107479 | ||||||
chr9:121107500
|
G | C | 1 | a0001c0001t0001g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.809-302G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121107500 | ||||||
chr9:121107558
|
C | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.809-244C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121107558 | ||||||
chr9:121107595
|
T | G | 1 | a0002c0002t0001g0061 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.809-207T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121107595 | ||||||
chr9:121107611
|
A | G | 4 | a0001c0001t0001g0147a0001c0001t0001g0172a0001c0001t0001g0173others(1): Show | 4 | HG00438.hp1 HG01074.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-191A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121107611 | ||||||
chr9:121107667
|
A | G | 2 | a0002c0006t0001g0025a0002c0006t0001g0026 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.809-135A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 7/43 | chr9 | 121107667 | ||||||
chr9:121108185
|
G | A | 191 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(188): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1002+190G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121108185 | ||||||
chr9:121108403
|
T | C | 111 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(108): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1002+408T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121108403 | ||||||
chr9:121108445
|
A | G | 1 | a0003c0003t0001g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1002+450A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121108445 | ||||||
chr9:121108509
|
T | A | 67 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(64): Show | 72 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.1002+514T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121108509 | ||||||
chr9:121108606
|
A | G | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(252): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1002+611A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121108606 | ||||||
chr9:121108660
|
G | A | 51 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(48): Show | 56 | HG00597.hp2 HG01081.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.1002+665G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121108660 | ||||||
chr9:121108733
|
A | G | 1 | a0003c0003t0001g0290 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1002+738A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121108733 | ||||||
chr9:121108865
|
G | T | 1 | a0002c0002t0001g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1002+870G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121108865 | ||||||
chr9:121108966
|
G | A | 1 | a0003c0003t0001g0281 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1002+971G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121108966 | ||||||
chr9:121109034
|
A | G | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1002+1039A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121109034 | ||||||
chr9:121109061
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1002+1066C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121109061 | ||||||
chr9:121109203
|
A | G | 178 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(175): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1002+1208A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121109203 | ||||||
chr9:121109421
|
G | A | 193 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(190): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1002+1426G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121109421 | ||||||
chr9:121109496
|
TTTAG | T | 4 | a0001c0001t0003g0238a0001c0001t0003g0242a0001c0001t0003g0243others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002+1506_1002+150 others(8): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 121109496 | |||||
chr9:121109577
|
C | CTG | 190 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(187): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.1002+1598_1002+159 others(6): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 121109577 | |||||
chr9:121109577
|
C | CTGTG | 3 | a0006c0010t0001g0052a0006c0010t0001g0090a0006c0010t0001g0091 | 3 | HG01070.hp1 HG02698.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1002+1596_1002+159 others(8): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 121109577 | |||||
chr9:121109710
|
G | T | 1 | a0004c0007t0001g0139 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1002+1715G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121109710 | ||||||
chr9:121109760
|
C | A | 1 | a0003c0003t0001g0264 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1002+1765C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121109760 | ||||||
chr9:121109787
|
A | G | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1002+1792A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121109787 | ||||||
chr9:121109857
|
A | G | 2 | a0002c0006t0001g0023a0002c0006t0001g0024 | 2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1002+1862A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121109857 | ||||||
chr9:121109878
|
T | C | 179 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(176): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1002+1883T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121109878 | ||||||
chr9:121110025
|
A | G | 66 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(63): Show | 71 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.1002+2030A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121110025 | ||||||
chr9:121110100
|
T | C | 1 | a0005c0008t0001g0062 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1002+2105T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121110100 | ||||||
chr9:121110160
|
C | A | 1 | a0001c0001t0001g0164 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1002+2165C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121110160 | ||||||
chr9:121110477
|
C | G | 1 | a0002c0002t0001g0036 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1003-1982C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121110477 | ||||||
chr9:121110686
|
G | C | 1 | a0004c0026t0001g0135 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1003-1773G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121110686 | ||||||
chr9:121110691
|
C | T | 1 | a0003c0019t0002g0127 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1003-1768C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121110691 | ||||||
chr9:121110701
|
AT | A | 12 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0025others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1003-1749delT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 121110701 | |||||
chr9:121110732
|
G | C | 2 | a0002c0002t0001g0046a0002c0002t0001g0099 | 2 | HG01175.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1003-1727G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121110732 | ||||||
chr9:121110859
|
G | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1003-1600G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121110859 | ||||||
chr9:121110883
|
CAG | C | 3 | a0002c0002t0001g0005a0002c0002t0001g0035a0002c0002t0001g0098 | 4 | HG01081.hp2 HG01123.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1003-1574_1003-157 others(6): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | INFO_REALIGN_3_PRIME | chr9 | 121110883 | |||||
chr9:121110933
|
T | G | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(252): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1003-1526T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121110933 | ||||||
chr9:121110958
|
G | C | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1003-1501G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121110958 | ||||||
chr9:121110970
|
T | G | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1003-1489T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121110970 | ||||||
chr9:121110999
|
T | G | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1003-1460T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121110999 | ||||||
chr9:121111198
|
G | A | 6 | a0002c0002t0001g0051a0002c0002t0001g0057a0002c0002t0001g0063others(3): Show | 6 | HG01255.hp1 HG01257.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1003-1261G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121111198 | ||||||
chr9:121111279
|
G | A | 1 | a0003c0003t0001g0259 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1003-1180G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121111279 | ||||||
chr9:121111375
|
C | A | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1003-1084C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121111375 | ||||||
chr9:121111433
|
A | T | 1 | a0003c0003t0001g0275 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1003-1026A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121111433 | ||||||
chr9:121111829
|
AG | A | 72 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(69): Show | 77 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.1003-629delG | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121111829 | ||||||
chr9:121111986
|
C | T | 1 | a0015c0024t0001g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1003-473C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121111986 | ||||||
chr9:121112430
|
T | C | 1 | a0001c0001t0003g0244 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1003-29T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 8/43 | chr9 | 121112430 | ||||||
chr9:121112884
|
C | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1122+306C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 9/43 | chr9 | 121112884 | ||||||
chr9:121113114
|
C | T | 193 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(190): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1123-388C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 9/43 | chr9 | 121113114 | ||||||
chr9:121113152
|
T | C | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(252): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1123-350T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 9/43 | chr9 | 121113152 | ||||||
chr9:121113310
|
A | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1123-192A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 9/43 | chr9 | 121113310 | ||||||
chr9:121113331
|
T | C | 3 | a0008c0012t0002g0142a0008c0012t0002g0143a0008c0012t0002g0144 | 3 | HG02976.hp1 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1123-171T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 9/43 | chr9 | 121113331 | ||||||
chr9:121113418
|
T | C | 1 | a0003c0003t0001g0118 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1123-84T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 9/43 | chr9 | 121113418 | ||||||
chr9:121113751
|
TA | T | 71 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(68): Show | 74 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.1345+36delA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 10/43 | INFO_REALIGN_3_PRIME | chr9 | 121113751 | |||||
chr9:121114027
|
G | A | 178 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(175): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1345+303G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 10/43 | chr9 | 121114027 | ||||||
chr9:121114132
|
C | T | 3 | a0008c0012t0002g0142a0008c0012t0002g0143a0008c0012t0002g0144 | 3 | HG02976.hp1 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1345+408C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 10/43 | chr9 | 121114132 | ||||||
chr9:121114169
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1345+445C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 10/43 | chr9 | 121114169 | ||||||
chr9:121114173
|
A | G | 94 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(91): Show | 99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1345+449A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 10/43 | chr9 | 121114173 | ||||||
chr9:121114268
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1345+544A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 10/43 | chr9 | 121114268 | ||||||
chr9:121114344
|
A | T | 1 | a0001c0001t0001g0223 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1345+620A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 10/43 | chr9 | 121114344 | ||||||
chr9:121114628
|
T | C | 1 | a0002c0002t0001g0036 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1346-463T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 10/43 | chr9 | 121114628 | ||||||
chr9:121115578
|
G | C | 2 | a0002c0006t0001g0027a0002c0006t0001g0028 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1455+378G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121115578 | ||||||
chr9:121115772
|
G | A | 247 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(244): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.1455+572G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121115772 | ||||||
chr9:121116045
|
G | GA | 9 | a0002c0002t0001g0059a0002c0002t0001g0066a0003c0003t0001g0116others(6): Show | 9 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.1455+853dupA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | INFO_REALIGN_3_PRIME | chr9 | 121116045 | |||||
chr9:121116076
|
G | A | 253 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(250): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1455+876G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121116076 | ||||||
chr9:121116384
|
T | A | 177 | a0001c0001t0001g0194a0002c0002t0001g0001a0002c0002t0001g0005others(174): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1455+1184T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121116384 | ||||||
chr9:121116386
|
A | T | 247 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(244): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.1455+1186A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121116386 | ||||||
chr9:121116387
|
T | A | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1455+1187T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121116387 | ||||||
chr9:121116519
|
C | G | 7 | a0003c0003t0001g0116a0003c0003t0001g0117a0003c0003t0001g0260others(4): Show | 7 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1455+1319C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121116519 | ||||||
chr9:121116544
|
A | T | 1 | a0003c0003t0001g0281 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1455+1344A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121116544 | ||||||
chr9:121116561
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1455+1361G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121116561 | ||||||
chr9:121116569
|
C | T | 7 | a0003c0003t0001g0116a0003c0003t0001g0117a0003c0003t0001g0260others(4): Show | 7 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.1455+1369C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121116569 | ||||||
chr9:121116570
|
G | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1455+1370G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121116570 | ||||||
chr9:121116975
|
A | G | 1 | a0002c0002t0001g0080 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1456-1371A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121116975 | ||||||
chr9:121117145
|
C | T | 1 | a0004c0007t0001g0010 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1456-1201C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121117145 | ||||||
chr9:121117288
|
A | G | 1 | a0003c0003t0001g0290 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1456-1058A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121117288 | ||||||
chr9:121117379
|
CTT | C | 13 | a0003c0004t0002g0009a0003c0004t0002g0124a0003c0004t0002g0125others(10): Show | 14 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1456-966_1456-965d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121117379 | ||||||
chr9:121117489
|
A | G | 106 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(103): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1456-857A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121117489 | ||||||
chr9:121117497
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1456-849A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121117497 | ||||||
chr9:121117612
|
A | C | 1 | a0003c0004t0002g0130 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1456-734A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121117612 | ||||||
chr9:121117627
|
T | A | 1 | a0003c0004t0002g0130 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1456-719T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121117627 | ||||||
chr9:121117807
|
A | G | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(246): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1456-539A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121117807 | ||||||
chr9:121117852
|
G | A | 3 | a0003c0003t0001g0018a0003c0003t0001g0264a0003c0003t0001g0265 | 4 | HG03490.hp1 HG03492.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1456-494G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121117852 | ||||||
chr9:121117935
|
C | T | 1 | a0002c0002t0001g0079 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1456-411C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121117935 | ||||||
chr9:121118240
|
A | T | 1 | a0002c0002t0001g0065 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1456-106A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121118240 | ||||||
chr9:121118292
|
T | C | 15 | a0003c0004t0001g0140a0003c0004t0002g0009a0003c0004t0002g0123others(12): Show | 16 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.1456-54T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121118292 | ||||||
chr9:121118298
|
A | T | 1 | a0002c0002t0001g0079 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1456-48A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121118298 | ||||||
chr9:121118341
|
A | G | 1 | a0002c0002t0001g0078 | 1 | NA18968.hp1 | splice_region_variant&intron_variant | LOW | c.1456-5A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 11/43 | chr9 | 121118341 | ||||||
chr9:121118906
|
G | A | 3 | a0008c0012t0002g0142a0008c0012t0002g0143a0008c0012t0002g0144 | 3 | HG02976.hp1 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1650+366G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121118906 | ||||||
chr9:121118921
|
T | C | 178 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(175): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1650+381T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121118921 | ||||||
chr9:121119080
|
A | ATG | 103 | a0001c0032t0001g0190a0002c0002t0001g0005a0002c0002t0001g0006others(100): Show | 109 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.1650+566_1650+567d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 121119080 | |||||
chr9:121119080
|
A | ATGTG | 50 | a0001c0005t0001g0184a0002c0002t0001g0001a0002c0002t0001g0022others(47): Show | 52 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.1650+564_1650+567d others(6): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 121119080 | |||||
chr9:121119080
|
A | ATGTGTG | 19 | a0002c0002t0001g0049a0002c0002t0001g0074a0002c0002t0001g0075others(16): Show | 19 | HG01069.hp1 HG01071.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.1650+562_1650+567d others(8): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 121119080 | |||||
chr9:121119080
|
A | G | 1 | a0002c0006t0001g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1650+540A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121119080 | ||||||
chr9:121119080
|
ATG | A | 6 | a0001c0001t0001g0147a0001c0001t0001g0172a0001c0001t0001g0196others(3): Show | 6 | HG01074.hp2 HG01884.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1650+566_1650+567d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 121119080 | |||||
chr9:121119080
|
ATGTG | A | 18 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0125others(15): Show | 19 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1650+564_1650+567d others(6): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 121119080 | |||||
chr9:121119108
|
A | G | 1 | a0010c0014t0001g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1650+568A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121119108 | ||||||
chr9:121119161
|
G | C | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1650+621G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121119161 | ||||||
chr9:121119224
|
A | C | 1 | a0002c0006t0001g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1650+684A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121119224 | ||||||
chr9:121119313
|
C | CT | 25 | a0001c0001t0001g0201a0001c0001t0001g0210a0002c0002t0001g0085others(22): Show | 27 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1650+787dupT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 121119313 | |||||
chr9:121119320
|
T | G | 1 | a0001c0001t0001g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1650+780T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121119320 | ||||||
chr9:121119331
|
C | G | 1 | a0003c0004t0002g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1650+791C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121119331 | ||||||
chr9:121119490
|
C | T | 290 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(287): Show | 308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.1650+950C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121119490 | ||||||
chr9:121119539
|
C | T | 2 | a0002c0006t0001g0027a0002c0006t0001g0028 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1650+999C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121119539 | ||||||
chr9:121119618
|
C | A | 1 | a0001c0005t0001g0015 | 2 | NA18971.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1650+1078C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121119618 | ||||||
chr9:121119703
|
T | G | 1 | a0002c0002t0002g0114 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1650+1163T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121119703 | ||||||
chr9:121119889
|
G | A | 1 | a0001c0005t0001g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1650+1349G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121119889 | ||||||
chr9:121120120
|
G | GT | 69 | a0001c0009t0001g0156a0002c0002t0001g0061a0003c0003t0001g0004others(66): Show | 74 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.1650+1590dupT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 121120120 | |||||
chr9:121120120
|
GT | G | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1650+1590delT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 121120120 | |||||
chr9:121120253
|
A | G | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1650+1713A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121120253 | ||||||
chr9:121120272
|
C | G | 1 | a0003c0004t0001g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1650+1732C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121120272 | ||||||
chr9:121120409
|
G | C | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1650+1869G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121120409 | ||||||
chr9:121120494
|
C | T | 2 | a0002c0006t0001g0027a0002c0006t0001g0028 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1650+1954C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121120494 | ||||||
chr9:121120756
|
G | A | 253 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(250): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1650+2216G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121120756 | ||||||
chr9:121120829
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1650+2289G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121120829 | ||||||
chr9:121120842
|
A | T | 1 | a0003c0003t0001g0295 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1650+2302A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121120842 | ||||||
chr9:121121530
|
T | C | 1 | a0001c0032t0001g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1651-2401T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121121530 | ||||||
chr9:121121658
|
A | C | 1 | a0016c0020t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1651-2273A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121121658 | ||||||
chr9:121121839
|
G | A | 1 | a0003c0004t0002g0130 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1651-2092G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121121839 | ||||||
chr9:121121952
|
G | A | 1 | a0002c0002t0001g0067 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1651-1979G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121121952 | ||||||
chr9:121121954
|
A | T | 3 | a0002c0002t0001g0005a0002c0002t0001g0035a0002c0002t0001g0098 | 4 | HG01081.hp2 HG01123.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1651-1977A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121121954 | ||||||
chr9:121122024
|
T | C | 1 | a0002c0002t0001g0079 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1651-1907T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121122024 | ||||||
chr9:121122028
|
A | G | 193 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(190): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1651-1903A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121122028 | ||||||
chr9:121122072
|
A | G | 1 | a0025c0027t0001g0193 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1651-1859A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121122072 | ||||||
chr9:121122085
|
T | G | 1 | a0004c0007t0001g0010 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1651-1846T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121122085 | ||||||
chr9:121122430
|
A | C | 1 | a0003c0003t0001g0289 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1651-1501A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121122430 | ||||||
chr9:121122606
|
T | C | 3 | a0003c0003t0001g0277a0003c0003t0001g0282a0003c0003t0001g0283 | 3 | NA18952.hp1 NA18975.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1651-1325T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121122606 | ||||||
chr9:121122758
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1651-1173C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121122758 | ||||||
chr9:121122824
|
A | G | 1 | a0002c0002t0001g0006 | 2 | HG02155.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1651-1107A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121122824 | ||||||
chr9:121122869
|
C | T | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1651-1062C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121122869 | ||||||
chr9:121122931
|
C | T | 2 | a0011c0013t0001g0248a0011c0013t0001g0249 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1651-1000C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121122931 | ||||||
chr9:121122997
|
G | A | 253 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(250): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1651-934G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121122997 | ||||||
chr9:121123162
|
G | GA | 77 | a0002c0002t0001g0041a0002c0002t0001g0061a0002c0002t0001g0101others(74): Show | 82 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.1651-763dupA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | INFO_REALIGN_3_PRIME | chr9 | 121123162 | |||||
chr9:121123352
|
G | A | 5 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1651-579G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121123352 | ||||||
chr9:121123374
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1651-557G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121123374 | ||||||
chr9:121123450
|
C | A | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(252): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1651-481C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121123450 | ||||||
chr9:121123458
|
G | A | 12 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0025others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1651-473G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121123458 | ||||||
chr9:121123580
|
T | C | 193 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(190): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1651-351T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121123580 | ||||||
chr9:121123652
|
G | A | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1651-279G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121123652 | ||||||
chr9:121123877
|
T | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0189 | 3 | HG01167.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1651-54T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 12/43 | chr9 | 121123877 | ||||||
chr9:121124425
|
G | A | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1804+341G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121124425 | ||||||
chr9:121124455
|
G | C | 193 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(190): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1804+371G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121124455 | ||||||
chr9:121124489
|
A | G | 1 | a0003c0004t0002g0125 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1804+405A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121124489 | ||||||
chr9:121124534
|
A | G | 1 | a0003c0003t0001g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1804+450A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121124534 | ||||||
chr9:121124656
|
G | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0180 | 2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1804+572G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121124656 | ||||||
chr9:121124764
|
C | T | 1 | a0001c0001t0003g0239 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1804+680C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121124764 | ||||||
chr9:121124774
|
C | CA | 99 | a0001c0001t0001g0153a0001c0001t0001g0164a0001c0001t0001g0177others(96): Show | 104 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1804+708dupA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | INFO_REALIGN_3_PRIME | chr9 | 121124774 | |||||
chr9:121124774
|
C | CAA | 10 | a0002c0002t0001g0038a0002c0002t0001g0046a0002c0002t0001g0095others(7): Show | 10 | HG00140.hp1 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1804+707_1804+708d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | INFO_REALIGN_3_PRIME | chr9 | 121124774 | |||||
chr9:121124774
|
CA | C | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1804+708delA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | INFO_REALIGN_3_PRIME | chr9 | 121124774 | |||||
chr9:121124809
|
G | T | 11 | a0003c0004t0002g0009a0003c0004t0002g0125a0003c0004t0002g0129others(8): Show | 12 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1804+725G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121124809 | ||||||
chr9:121124944
|
GA | G | 243 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(240): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1805-757delA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | INFO_REALIGN_3_PRIME | chr9 | 121124944 | |||||
chr9:121124944
|
GAA | G | 6 | a0001c0001t0001g0217a0001c0001t0001g0225a0001c0001t0001g0226others(3): Show | 6 | HG02015.hp1 HG02132.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.1805-758_1805-757d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | INFO_REALIGN_3_PRIME | chr9 | 121124944 | |||||
chr9:121125049
|
G | T | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1805-667G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121125049 | ||||||
chr9:121125067
|
C | T | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1805-649C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121125067 | ||||||
chr9:121125092
|
A | G | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(252): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1805-624A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121125092 | ||||||
chr9:121125138
|
G | C | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(246): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1805-578G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121125138 | ||||||
chr9:121125170
|
CT | C | 5 | a0002c0002t0001g0007a0002c0002t0001g0008a0002c0002t0001g0050others(2): Show | 7 | HG00621.hp2 HG02071.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1805-531delT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | INFO_REALIGN_3_PRIME | chr9 | 121125170 | |||||
chr9:121125199
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1805-517G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121125199 | ||||||
chr9:121125294
|
A | G | 1 | a0026c0033t0001g0170 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1805-422A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121125294 | ||||||
chr9:121125387
|
C | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1805-329C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121125387 | ||||||
chr9:121125434
|
C | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1805-282C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121125434 | ||||||
chr9:121125514
|
T | C | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1805-202T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 13/43 | chr9 | 121125514 | ||||||
chr9:121125964
|
G | T | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(252): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.2025+28G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121125964 | ||||||
chr9:121126200
|
T | C | 193 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(190): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.2025+264T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121126200 | ||||||
chr9:121126399
|
A | C | 1 | a0004c0007t0001g0010 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2025+463A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121126399 | ||||||
chr9:121126453
|
T | G | 1 | a0003c0003t0001g0260 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2025+517T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121126453 | ||||||
chr9:121126548
|
T | C | 9 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0027others(6): Show | 9 | HG01891.hp1 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2025+612T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121126548 | ||||||
chr9:121126559
|
A | G | 2 | a0002c0002t0001g0088a0002c0002t0001g0089 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2025+623A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121126559 | ||||||
chr9:121126818
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2025+882T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121126818 | ||||||
chr9:121126829
|
G | GT | 194 | a0001c0001t0001g0204a0002c0002t0001g0001a0002c0002t0001g0005others(191): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.2025+902dupT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr9 | 121126829 | |||||
chr9:121126839
|
G | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG02451.hp2 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2025+903G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121126839 | ||||||
chr9:121126982
|
G | A | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2025+1046G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121126982 | ||||||
chr9:121127041
|
A | G | 8 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0175others(5): Show | 8 | HG01496.hp2 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2025+1105A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121127041 | ||||||
chr9:121127088
|
C | T | 178 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(175): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.2025+1152C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121127088 | ||||||
chr9:121127458
|
C | G | 67 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(64): Show | 72 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.2025+1522C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121127458 | ||||||
chr9:121127525
|
C | A | 1 | a0002c0002t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2025+1589C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121127525 | ||||||
chr9:121127539
|
G | T | 12 | a0003c0004t0002g0009a0003c0004t0002g0125a0003c0004t0002g0128others(9): Show | 13 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.2025+1603G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121127539 | ||||||
chr9:121127621
|
T | G | 1 | a0002c0002t0001g0074 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2025+1685T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121127621 | ||||||
chr9:121127726
|
C | T | 13 | a0003c0004t0002g0009a0003c0004t0002g0124a0003c0004t0002g0125others(10): Show | 14 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.2025+1790C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121127726 | ||||||
chr9:121127738
|
G | A | 11 | a0003c0004t0002g0009a0003c0004t0002g0125a0003c0004t0002g0129others(8): Show | 12 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.2025+1802G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121127738 | ||||||
chr9:121127793
|
C | A | 1 | a0001c0001t0001g0196 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2025+1857C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121127793 | ||||||
chr9:121127860
|
A | G | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(246): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.2025+1924A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121127860 | ||||||
chr9:121127888
|
T | TG | 67 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(64): Show | 72 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.2025+1953dupG | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr9 | 121127888 | |||||
chr9:121127973
|
C | T | 1 | a0001c0005t0001g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2025+2037C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121127973 | ||||||
chr9:121128031
|
A | G | 72 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(69): Show | 77 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.2025+2095A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128031 | ||||||
chr9:121128137
|
T | A | 1 | a0003c0004t0002g0134 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2025+2201T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128137 | ||||||
chr9:121128158
|
C | A | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2025+2222C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128158 | ||||||
chr9:121128171
|
C | G | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2025+2235C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128171 | ||||||
chr9:121128171
|
C | T | 94 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(91): Show | 99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.2025+2235C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128171 | ||||||
chr9:121128215
|
G | A | 1 | a0019c0016t0002g0021 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2025+2279G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128215 | ||||||
chr9:121128391
|
G | A | 1 | a0002c0002t0001g0022 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2025+2455G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128391 | ||||||
chr9:121128459
|
A | G | 2 | a0003c0004t0002g0141a0003c0004t0002g0145 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2025+2523A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128459 | ||||||
chr9:121128588
|
G | A | 1 | a0003c0003t0001g0286 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2025+2652G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128588 | ||||||
chr9:121128611
|
A | G | 2 | a0002c0002t0001g0005a0002c0002t0001g0035 | 3 | HG01123.hp1 HG01361.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2025+2675A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128611 | ||||||
chr9:121128662
|
T | A | 9 | a0002c0002t0001g0049a0002c0002t0001g0074a0002c0002t0001g0075others(6): Show | 9 | NA18950.hp1 NA18951.hp2 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.2025+2726T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128662 | ||||||
chr9:121128722
|
T | G | 11 | a0003c0003t0001g0116a0003c0003t0001g0117a0003c0003t0001g0250others(8): Show | 11 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.2025+2786T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128722 | ||||||
chr9:121128829
|
G | A | 1 | a0003c0003t0001g0253 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2025+2893G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128829 | ||||||
chr9:121128888
|
T | TTAAA | 253 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(250): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.2025+2954_2025+295 others(8): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr9 | 121128888 | |||||
chr9:121128955
|
G | A | 7 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0027others(4): Show | 7 | HG01891.hp1 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2025+3019G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128955 | ||||||
chr9:121128989
|
C | A | 1 | a0003c0003t0001g0281 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2025+3053C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121128989 | ||||||
chr9:121129073
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0189 | 3 | HG01167.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2025+3137G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121129073 | ||||||
chr9:121129136
|
T | C | 1 | a0010c0014t0001g0167 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2025+3200T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121129136 | ||||||
chr9:121129152
|
A | C | 1 | a0002c0002t0001g0074 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2025+3216A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121129152 | ||||||
chr9:121129281
|
T | G | 1 | a0003c0003t0001g0117 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2025+3345T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121129281 | ||||||
chr9:121129298
|
G | A | 191 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(188): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.2025+3362G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121129298 | ||||||
chr9:121129615
|
A | G | 1 | a0025c0027t0001g0193 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2025+3679A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121129615 | ||||||
chr9:121129706
|
T | C | 92 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(89): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2025+3770T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121129706 | ||||||
chr9:121129769
|
G | C | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG00408.hp2 HG02129.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.2025+3833G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121129769 | ||||||
chr9:121129769
|
G | T | 106 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(103): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2025+3833G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121129769 | ||||||
chr9:121129958
|
C | G | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2025+4022C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121129958 | ||||||
chr9:121130227
|
C | G | 1 | a0013c0021t0001g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2025+4291C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121130227 | ||||||
chr9:121130308
|
T | G | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2025+4372T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121130308 | ||||||
chr9:121130387
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2025+4451A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121130387 | ||||||
chr9:121130440
|
G | A | 92 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(89): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2025+4504G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121130440 | ||||||
chr9:121130477
|
C | T | 191 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(188): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.2025+4541C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121130477 | ||||||
chr9:121130811
|
T | C | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(246): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.2025+4875T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121130811 | ||||||
chr9:121131056
|
T | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2026-4750T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121131056 | ||||||
chr9:121131215
|
A | G | 1 | a0001c0001t0001g0173 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2026-4591A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121131215 | ||||||
chr9:121131385
|
A | T | 1 | a0003c0003t0001g0291 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2026-4421A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121131385 | ||||||
chr9:121131450
|
C | T | 1 | a0002c0002t0001g0072 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2026-4356C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121131450 | ||||||
chr9:121131700
|
G | A | 1 | a0003c0004t0002g0124 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2026-4106G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121131700 | ||||||
chr9:121131770
|
C | T | 104 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(101): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.2026-4036C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121131770 | ||||||
chr9:121131771
|
G | C | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2026-4035G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121131771 | ||||||
chr9:121131772
|
G | A | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2026-4034G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121131772 | ||||||
chr9:121131995
|
G | C | 1 | a0003c0003t0001g0269 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2026-3811G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121131995 | ||||||
chr9:121132038
|
G | A | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2026-3768G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121132038 | ||||||
chr9:121132075
|
T | C | 1 | a0003c0003t0001g0265 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2026-3731T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121132075 | ||||||
chr9:121132337
|
C | G | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2026-3469C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121132337 | ||||||
chr9:121132386
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2026-3420T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121132386 | ||||||
chr9:121132439
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2026-3367T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121132439 | ||||||
chr9:121132581
|
G | A | 29 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0164others(26): Show | 32 | HG00280.hp1 HG00438.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.2026-3225G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121132581 | ||||||
chr9:121132773
|
T | C | 1 | a0003c0003t0001g0117 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2026-3033T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121132773 | ||||||
chr9:121132941
|
T | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2026-2865T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121132941 | ||||||
chr9:121133056
|
C | T | 1 | a0003c0003t0001g0117 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2026-2750C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121133056 | ||||||
chr9:121133129
|
T | G | 12 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0025others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2026-2677T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121133129 | ||||||
chr9:121133258
|
A | C | 47 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(44): Show | 49 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.2026-2548A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121133258 | ||||||
chr9:121133296
|
C | T | 1 | a0003c0003t0001g0289 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2026-2510C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121133296 | ||||||
chr9:121133322
|
G | A | 1 | a0002c0002t0001g0035 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2026-2484G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121133322 | ||||||
chr9:121133480
|
G | A | 14 | a0003c0003t0001g0020a0003c0003t0001g0118a0003c0003t0001g0119others(11): Show | 15 | HG01081.hp1 HG01123.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.2026-2326G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121133480 | ||||||
chr9:121133507
|
G | A | 1 | a0002c0002t0001g0006 | 2 | HG02155.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2026-2299G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121133507 | ||||||
chr9:121133568
|
T | G | 1 | a0001c0001t0001g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2026-2238T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121133568 | ||||||
chr9:121133594
|
C | T | 1 | a0003c0004t0002g0133 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2026-2212C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121133594 | ||||||
chr9:121133702
|
T | G | 1 | a0021c0030t0001g0235 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2026-2104T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121133702 | ||||||
chr9:121133732
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2026-2074G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121133732 | ||||||
chr9:121133915
|
C | G | 1 | a0002c0023t0001g0092 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2026-1891C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121133915 | ||||||
chr9:121134230
|
G | A | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2026-1576G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121134230 | ||||||
chr9:121134260
|
G | A | 1 | a0002c0002t0001g0045 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2026-1546G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121134260 | ||||||
chr9:121134291
|
TTA | T | 6 | a0002c0002t0001g0083a0002c0002t0001g0104a0002c0002t0001g0306others(3): Show | 6 | HG00639.hp2 HG01515.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.2026-1513_2026-151 others(6): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr9 | 121134291 | |||||
chr9:121134292
|
TA | T | 168 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(165): Show | 178 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.2026-1513delA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121134292 | ||||||
chr9:121134293
|
A | T | 14 | a0002c0002t0001g0042a0003c0004t0002g0009a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2026-1513A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121134293 | ||||||
chr9:121134293
|
AT | A | 66 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(63): Show | 69 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.2026-1498delT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr9 | 121134293 | |||||
chr9:121134297
|
T | A | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.2026-1509T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121134297 | ||||||
chr9:121134376
|
C | T | 67 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(64): Show | 72 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.2026-1430C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121134376 | ||||||
chr9:121134541
|
C | T | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2026-1265C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121134541 | ||||||
chr9:121134648
|
A | ATG | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2026-1145_2026-114 others(6): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | INFO_REALIGN_3_PRIME | chr9 | 121134648 | |||||
chr9:121134670
|
G | A | 13 | a0003c0004t0002g0009a0003c0004t0002g0124a0003c0004t0002g0125others(10): Show | 14 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.2026-1136G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121134670 | ||||||
chr9:121134698
|
A | G | 1 | a0003c0003t0001g0274 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2026-1108A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121134698 | ||||||
chr9:121135036
|
G | A | 4 | a0003c0003t0001g0250a0003c0003t0001g0251a0011c0013t0001g0248others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.2026-770G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121135036 | ||||||
chr9:121135217
|
A | G | 7 | a0003c0003t0001g0116a0003c0003t0001g0117a0003c0003t0001g0260others(4): Show | 7 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.2026-589A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121135217 | ||||||
chr9:121135231
|
C | T | 1 | a0004c0026t0001g0135 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2026-575C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121135231 | ||||||
chr9:121135347
|
C | T | 7 | a0002c0002t0001g0040a0002c0002t0001g0044a0002c0002t0001g0081others(4): Show | 7 | HG02083.hp2 HG02132.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.2026-459C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121135347 | ||||||
chr9:121135515
|
C | G | 1 | a0001c0001t0001g0219 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2026-291C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121135515 | ||||||
chr9:121135543
|
C | T | 12 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0025others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2026-263C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121135543 | ||||||
chr9:121135617
|
C | T | 1 | a0003c0003t0001g0276 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2026-189C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121135617 | ||||||
chr9:121135702
|
C | G | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2026-104C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 14/43 | chr9 | 121135702 | ||||||
chr9:121136377
|
A | T | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(246): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.2202+395A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121136377 | ||||||
chr9:121136414
|
A | G | 1 | a0003c0003t0001g0265 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2202+432A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121136414 | ||||||
chr9:121136456
|
C | T | 1 | a0002c0023t0001g0092 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2202+474C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121136456 | ||||||
chr9:121136611
|
G | A | 71 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(68): Show | 76 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.2202+629G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121136611 | ||||||
chr9:121136834
|
C | G | 1 | a0002c0002t0001g0071 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2202+852C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121136834 | ||||||
chr9:121137065
|
A | G | 1 | a0021c0030t0001g0235 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2202+1083A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121137065 | ||||||
chr9:121137083
|
G | A | 3 | a0004c0007t0001g0136a0004c0007t0001g0137a0004c0007t0001g0138 | 3 | HG02451.hp1 HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2202+1101G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121137083 | ||||||
chr9:121137221
|
C | T | 1 | a0002c0002t0001g0055 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2202+1239C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121137221 | ||||||
chr9:121137349
|
A | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2203-1196A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121137349 | ||||||
chr9:121137736
|
TAATA | T | 57 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(54): Show | 59 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.2203-802_2203-799d others(6): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | INFO_REALIGN_3_PRIME | chr9 | 121137736 | |||||
chr9:121137894
|
A | G | 1 | a0003c0003t0001g0298 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2203-651A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121137894 | ||||||
chr9:121138033
|
T | C | 7 | a0003c0003t0001g0256a0004c0007t0001g0010a0004c0007t0001g0136others(4): Show | 8 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2203-512T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121138033 | ||||||
chr9:121138169
|
T | C | 2 | a0003c0003t0001g0252a0003c0003t0001g0274 | 2 | NA18997.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.2203-376T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121138169 | ||||||
chr9:121138171
|
C | T | 1 | a0002c0002t0001g0113 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2203-374C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121138171 | ||||||
chr9:121138252
|
C | T | 7 | a0002c0002t0001g0034a0002c0002t0001g0041a0002c0002t0001g0048others(4): Show | 7 | HG01978.hp1 HG02129.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.2203-293C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121138252 | ||||||
chr9:121138501
|
A | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2203-44A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 15/43 | chr9 | 121138501 | ||||||
chr9:121138762
|
G | A | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2337+83G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121138762 | ||||||
chr9:121139062
|
G | A | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2337+383G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121139062 | ||||||
chr9:121139316
|
T | G | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(246): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.2337+637T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121139316 | ||||||
chr9:121139344
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2337+665C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121139344 | ||||||
chr9:121139490
|
C | G | 1 | a0019c0016t0002g0021 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2337+811C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121139490 | ||||||
chr9:121139520
|
A | G | 1 | a0003c0003t0001g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2337+841A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121139520 | ||||||
chr9:121139664
|
G | T | 8 | a0002c0002t0001g0001a0002c0002t0001g0038a0002c0002t0001g0042others(5): Show | 9 | HG03654.hp1 NA18956.hp2 NA18974.hp1 others(6): Show |
intron_variant | MODIFIER | c.2338-977G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121139664 | ||||||
chr9:121139783
|
G | A | 8 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2338-858G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121139783 | ||||||
chr9:121139801
|
T | A | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2338-840T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121139801 | ||||||
chr9:121139858
|
G | T | 1 | a0021c0030t0001g0235 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2338-783G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121139858 | ||||||
chr9:121140125
|
T | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2338-516T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121140125 | ||||||
chr9:121140140
|
T | G | 2 | a0003c0004t0002g0141a0003c0004t0002g0145 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2338-501T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121140140 | ||||||
chr9:121140297
|
G | A | 1 | a0003c0003t0001g0284 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2338-344G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121140297 | ||||||
chr9:121140407
|
G | C | 2 | a0002c0002t0001g0104a0002c0002t0001g0105 | 2 | HG00741.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2338-234G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121140407 | ||||||
chr9:121140429
|
A | G | 2 | a0002c0002t0001g0041a0002c0002t0001g0080 | 2 | HG02129.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.2338-212A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121140429 | ||||||
chr9:121140436
|
T | C | 1 | a0004c0007t0001g0010 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2338-205T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121140436 | ||||||
chr9:121140580
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2338-61C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 16/43 | chr9 | 121140580 | ||||||
chr9:121140839
|
T | C | 1 | a0002c0002t0001g0072 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2483+53T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 17/43 | chr9 | 121140839 | ||||||
chr9:121140967
|
A | G | 3 | a0001c0001t0001g0218a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG02451.hp2 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2483+181A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 17/43 | chr9 | 121140967 | ||||||
chr9:121141014
|
A | G | 4 | a0004c0007t0001g0136a0004c0007t0001g0137a0004c0007t0001g0138others(1): Show | 4 | HG02451.hp1 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2483+228A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 17/43 | chr9 | 121141014 | ||||||
chr9:121141146
|
A | G | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(252): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.2484-235A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 17/43 | chr9 | 121141146 | ||||||
chr9:121141196
|
C | G | 1 | a0002c0002t0001g0053 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2484-185C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 17/43 | chr9 | 121141196 | ||||||
chr9:121141742
|
C | T | 2 | a0003c0004t0002g0141a0003c0004t0002g0145 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2691+154C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 18/43 | chr9 | 121141742 | ||||||
chr9:121141836
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0001g0236 | 2 | HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2691+248G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 18/43 | chr9 | 121141836 | ||||||
chr9:121141889
|
T | A | 72 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(69): Show | 77 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.2692-202T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 18/43 | chr9 | 121141889 | ||||||
chr9:121141926
|
A | G | 1 | a0002c0002t0001g0045 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2692-165A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 18/43 | chr9 | 121141926 | ||||||
chr9:121142504
|
G | T | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2871+234G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 19/43 | chr9 | 121142504 | ||||||
chr9:121142670
|
T | C | 1 | a0003c0019t0002g0127 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2871+400T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 19/43 | chr9 | 121142670 | ||||||
chr9:121142913
|
C | CT | 26 | a0001c0001t0001g0197a0001c0001t0001g0218a0001c0001t0001g0219others(23): Show | 26 | HG01109.hp1 HG01261.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.2871+655dupT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 121142913 | |||||
chr9:121142913
|
C | CTT | 31 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(28): Show | 33 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.2871+654_2871+655d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 19/43 | INFO_REALIGN_3_PRIME | chr9 | 121142913 | |||||
chr9:121143084
|
A | G | 94 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(91): Show | 99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.2871+814A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 19/43 | chr9 | 121143084 | ||||||
chr9:121143245
|
A | C | 6 | a0003c0003t0001g0018a0003c0003t0001g0264a0003c0003t0001g0265others(3): Show | 7 | HG03490.hp1 HG03492.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.2872-658A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 19/43 | chr9 | 121143245 | ||||||
chr9:121143357
|
C | G | 106 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(103): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2872-546C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 19/43 | chr9 | 121143357 | ||||||
chr9:121143425
|
T | G | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2872-478T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 19/43 | chr9 | 121143425 | ||||||
chr9:121143723
|
A | C | 193 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(190): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.2872-180A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 19/43 | chr9 | 121143723 | ||||||
chr9:121143821
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2872-82G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 19/43 | chr9 | 121143821 | ||||||
chr9:121143827
|
A | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2872-76A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 19/43 | chr9 | 121143827 | ||||||
chr9:121144353
|
G | A | 2 | a0003c0003t0001g0250a0003c0003t0001g0251 | 2 | HG03239.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3051+271G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 20/43 | chr9 | 121144353 | ||||||
chr9:121144526
|
G | T | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.3052-317G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 20/43 | chr9 | 121144526 | ||||||
chr9:121145072
|
T | C | 1 | a0024c0031t0001g0154 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3168+113T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 21/43 | chr9 | 121145072 | ||||||
chr9:121145528
|
A | C | 245 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(242): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.3310+143A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 22/43 | chr9 | 121145528 | ||||||
chr9:121145590
|
C | T | 2 | a0010c0014t0001g0169a0020c0034t0001g0168 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3310+205C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 22/43 | chr9 | 121145590 | ||||||
chr9:121145812
|
C | G | 1 | a0002c0002t0001g0022 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3311-296C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 22/43 | chr9 | 121145812 | ||||||
chr9:121146067
|
G | A | 191 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(188): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.3311-41G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 22/43 | chr9 | 121146067 | ||||||
chr9:121146507
|
T | A | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.3459+251T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 23/43 | chr9 | 121146507 | ||||||
chr9:121147074
|
C | G | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3459+818C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 23/43 | chr9 | 121147074 | ||||||
chr9:121147085
|
T | C | 255 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(252): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.3459+829T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 23/43 | chr9 | 121147085 | ||||||
chr9:121147159
|
C | T | 1 | a0002c0002t0001g0050 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3459+903C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 23/43 | chr9 | 121147159 | ||||||
chr9:121147168
|
A | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3459+912A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 23/43 | chr9 | 121147168 | ||||||
chr9:121147466
|
T | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.3460-1206T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 23/43 | chr9 | 121147466 | ||||||
chr9:121147506
|
A | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3460-1166A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 23/43 | chr9 | 121147506 | ||||||
chr9:121147546
|
A | T | 1 | a0003c0004t0002g0131 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3460-1126A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 23/43 | chr9 | 121147546 | ||||||
chr9:121148067
|
A | C | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.3460-605A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 23/43 | chr9 | 121148067 | ||||||
chr9:121148132
|
G | A | 4 | a0002c0002t0001g0057a0002c0002t0001g0063a0002c0002t0001g0065others(1): Show | 4 | HG01255.hp1 HG01257.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.3460-540G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 23/43 | chr9 | 121148132 | ||||||
chr9:121148138
|
C | G | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.3460-534C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 23/43 | chr9 | 121148138 | ||||||
chr9:121148918
|
C | T | 2 | a0002c0006t0001g0025a0002c0006t0001g0026 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3649+57C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 24/43 | chr9 | 121148918 | ||||||
chr9:121149167
|
G | C | 71 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(68): Show | 76 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.3649+306G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 24/43 | chr9 | 121149167 | ||||||
chr9:121149392
|
C | CG | 234 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0195others(231): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.3649+531_3649+532i others(3): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 24/43 | chr9 | 121149392 | ||||||
chr9:121149392
|
C | CGT | 7 | a0001c0001t0001g0194a0002c0002t0001g0049a0002c0002t0001g0113others(4): Show | 7 | HG00738.hp2 HG01981.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.3649+531_3649+532i others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 24/43 | chr9 | 121149392 | ||||||
chr9:121149408
|
GT | G | 183 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(180): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.3649+558delT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 24/43 | INFO_REALIGN_3_PRIME | chr9 | 121149408 | |||||
chr9:121149559
|
C | T | 1 | a0003c0003t0001g0265 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3650-611C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 24/43 | chr9 | 121149559 | ||||||
chr9:121149637
|
C | T | 2 | a0002c0006t0001g0027a0002c0006t0001g0028 | 2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3650-533C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 24/43 | chr9 | 121149637 | ||||||
chr9:121150517
|
C | G | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01261.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3963+34C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121150517 | ||||||
chr9:121150738
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3963+255C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121150738 | ||||||
chr9:121150862
|
C | T | 1 | a0001c0009t0001g0155 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3963+379C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121150862 | ||||||
chr9:121151022
|
T | C | 8 | a0001c0001t0001g0195a0001c0001t0001g0217a0001c0001t0001g0223others(5): Show | 8 | HG00597.hp1 HG02015.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.3963+539T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121151022 | ||||||
chr9:121151384
|
C | CT | 5 | a0003c0003t0001g0118a0003c0003t0001g0250a0003c0003t0001g0296others(2): Show | 5 | HG01167.hp1 HG02071.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.3963+903dupT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 121151384 | |||||
chr9:121151384
|
C | CTT | 65 | a0002c0006t0001g0027a0003c0003t0001g0004a0003c0003t0001g0018others(62): Show | 71 | HG00099.hp2 HG00323.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.3963+902_3963+903d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 121151384 | |||||
chr9:121151384
|
C | CTTT | 20 | a0002c0002t0001g0022a0002c0002t0001g0058a0002c0002t0001g0059others(17): Show | 20 | HG01109.hp2 HG01256.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.3963+903_3963+904i others(5): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 121151384 | |||||
chr9:121151384
|
C | CTTTT | 81 | a0002c0002t0001g0005a0002c0002t0001g0006a0002c0002t0001g0007others(78): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.3963+903_3963+904i others(6): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 121151384 | |||||
chr9:121151384
|
C | CTTTTT | 15 | a0002c0002t0001g0001a0002c0002t0001g0038a0002c0002t0001g0043others(12): Show | 16 | HG01175.hp1 HG02486.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.3963+903_3963+904i others(7): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 121151384 | |||||
chr9:121151387
|
C | T | 186 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(183): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.3963+904C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121151387 | ||||||
chr9:121151387
|
CT | C | 8 | a0001c0001t0001g0189a0001c0001t0001g0213a0001c0001t0001g0216others(5): Show | 8 | HG01167.hp2 HG02080.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3963+925delT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | INFO_REALIGN_3_PRIME | chr9 | 121151387 | |||||
chr9:121151582
|
G | A | 61 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(58): Show | 66 | HG00597.hp2 HG01081.hp1 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.3964-903G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121151582 | ||||||
chr9:121151611
|
C | G | 1 | a0003c0004t0002g0134 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3964-874C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121151611 | ||||||
chr9:121151689
|
C | G | 1 | a0001c0001t0001g0216 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3964-796C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121151689 | ||||||
chr9:121151711
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3964-774T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121151711 | ||||||
chr9:121151714
|
T | C | 1 | a0003c0004t0002g0130 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3964-771T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121151714 | ||||||
chr9:121152028
|
A | G | 167 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(164): Show | 177 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.3964-457A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121152028 | ||||||
chr9:121152057
|
C | A | 1 | a0003c0003t0001g0272 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3964-428C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121152057 | ||||||
chr9:121152220
|
G | A | 1 | a0002c0002t0001g0068 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3964-265G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121152220 | ||||||
chr9:121152314
|
T | C | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(246): Show | 263 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.3964-171T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121152314 | ||||||
chr9:121152328
|
G | A | 14 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(11): Show | 15 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.3964-157G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 25/43 | chr9 | 121152328 | ||||||
chr9:121153222
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02015.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.4172+529C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 26/43 | chr9 | 121153222 | ||||||
chr9:121153369
|
G | A | 1 | a0026c0033t0001g0170 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4172+676G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 26/43 | chr9 | 121153369 | ||||||
chr9:121153491
|
C | CT | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.4172+806dupT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr9 | 121153491 | |||||
chr9:121153677
|
G | A | 17 | a0003c0004t0001g0140a0003c0004t0002g0124a0003c0004t0002g0125others(14): Show | 17 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.4172+984G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 26/43 | chr9 | 121153677 | ||||||
chr9:121153766
|
C | T | 1 | a0003c0003t0001g0253 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.4173-955C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 26/43 | chr9 | 121153766 | ||||||
chr9:121153828
|
C | T | 1 | a0003c0003t0001g0281 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.4173-893C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 26/43 | chr9 | 121153828 | ||||||
chr9:121154225
|
T | TA | 12 | a0003c0004t0002g0123a0003c0004t0002g0141a0003c0004t0002g0145others(9): Show | 13 | HG02451.hp1 HG02486.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.4173-494dupA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 26/43 | INFO_REALIGN_3_PRIME | chr9 | 121154225 | |||||
chr9:121154462
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4173-259T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 26/43 | chr9 | 121154462 | ||||||
chr9:121154596
|
A | G | 58 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(55): Show | 60 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.4173-125A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 26/43 | chr9 | 121154596 | ||||||
chr9:121154615
|
C | T | 6 | a0003c0004t0001g0140a0003c0004t0002g0141a0003c0004t0002g0145others(3): Show | 6 | HG00639.hp2 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.4173-106C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 26/43 | chr9 | 121154615 | ||||||
chr9:121154698
|
T | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.4173-23T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 26/43 | chr9 | 121154698 | ||||||
chr9:121155077
|
A | G | 247 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(244): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.4365+164A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/43 | chr9 | 121155077 | ||||||
chr9:121155164
|
A | G | 1 | a0002c0002t0001g0103 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4365+251A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/43 | chr9 | 121155164 | ||||||
chr9:121155259
|
C | T | 1 | a0016c0020t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4365+346C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/43 | chr9 | 121155259 | ||||||
chr9:121155335
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4365+422T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/43 | chr9 | 121155335 | ||||||
chr9:121155374
|
C | G | 1 | a0003c0003t0001g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4365+461C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/43 | chr9 | 121155374 | ||||||
chr9:121155624
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4365+711G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/43 | chr9 | 121155624 | ||||||
chr9:121155930
|
A | G | 10 | a0002c0002t0001g0049a0002c0002t0001g0074a0002c0002t0001g0075others(7): Show | 10 | NA18942.hp2 NA18950.hp1 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.4365+1017A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/43 | chr9 | 121155930 | ||||||
chr9:121156330
|
G | A | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4366-1140G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/43 | chr9 | 121156330 | ||||||
chr9:121156551
|
A | G | 1 | a0001c0001t0003g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4366-919A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/43 | chr9 | 121156551 | ||||||
chr9:121156628
|
T | C | 1 | a0003c0003t0001g0018 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.4366-842T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/43 | chr9 | 121156628 | ||||||
chr9:121156713
|
G | T | 1 | a0003c0003t0001g0299 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.4366-757G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/43 | chr9 | 121156713 | ||||||
chr9:121156752
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0189 | 3 | HG01167.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.4366-718T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/43 | chr9 | 121156752 | ||||||
chr9:121156757
|
T | TA | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0149others(246): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.4366-709dupA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/43 | INFO_REALIGN_3_PRIME | chr9 | 121156757 | |||||
chr9:121156762
|
C | A | 290 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(287): Show | 308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.4366-708C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 27/43 | chr9 | 121156762 | ||||||
chr9:121157635
|
T | G | 2 | a0002c0002t0001g0086a0002c0002t0001g0087 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.4496+35T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 28/43 | chr9 | 121157635 | ||||||
chr9:121158154
|
A | G | 1 | a0002c0002t0001g0060 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.4764+45A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 30/43 | chr9 | 121158154 | ||||||
chr9:121158280
|
A | G | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4764+171A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 30/43 | chr9 | 121158280 | ||||||
chr9:121158285
|
G | A | 187 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(184): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.4764+176G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 30/43 | chr9 | 121158285 | ||||||
chr9:121158362
|
C | T | 1 | a0003c0003t0001g0276 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4764+253C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 30/43 | chr9 | 121158362 | ||||||
chr9:121158607
|
C | T | 1 | a0002c0006t0001g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4765-248C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 30/43 | chr9 | 121158607 | ||||||
chr9:121158689
|
G | A | 1 | a0002c0006t0001g0028 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4765-166G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 30/43 | chr9 | 121158689 | ||||||
chr9:121158840
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4765-15T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 30/43 | chr9 | 121158840 | ||||||
chr9:121159330
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4929+311C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 31/43 | chr9 | 121159330 | ||||||
chr9:121159356
|
G | A | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.4929+337G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 31/43 | chr9 | 121159356 | ||||||
chr9:121159682
|
CA | C | 7 | a0001c0001t0001g0189a0002c0002t0001g0043a0002c0002t0001g0055others(4): Show | 7 | HG00323.hp1 HG01167.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.4930-446delA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 31/43 | INFO_REALIGN_3_PRIME | chr9 | 121159682 | |||||
chr9:121159999
|
G | A | 9 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(6): Show | 9 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.4930-144G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 31/43 | chr9 | 121159999 | ||||||
chr9:121160314
|
G | A | 1 | a0002c0002t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.5089+12G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 32/43 | chr9 | 121160314 | ||||||
chr9:121160451
|
A | ATGT | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(246): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.5089+150_5089+151i others(5): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr9 | 121160451 | |||||
chr9:121160558
|
G | C | 1 | a0002c0002t0001g0047 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5089+256G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 32/43 | chr9 | 121160558 | ||||||
chr9:121160649
|
G | A | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.5089+347G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 32/43 | chr9 | 121160649 | ||||||
chr9:121160751
|
A | T | 171 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(168): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.5089+449A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 32/43 | chr9 | 121160751 | ||||||
chr9:121160991
|
A | C | 1 | a0002c0002t0001g0078 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.5089+689A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 32/43 | chr9 | 121160991 | ||||||
chr9:121161133
|
A | AGT | 249 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(246): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.5090-711_5090-710d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 32/43 | INFO_REALIGN_3_PRIME | chr9 | 121161133 | |||||
chr9:121161160
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5090-696G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 32/43 | chr9 | 121161160 | ||||||
chr9:121161298
|
C | A | 1 | a0002c0006t0001g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5090-558C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 32/43 | chr9 | 121161298 | ||||||
chr9:121162389
|
CAT | C | 171 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(168): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.5423+120_5423+121d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr9 | 121162389 | |||||
chr9:121162436
|
CT | C | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.5423+178delT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr9 | 121162436 | |||||
chr9:121162921
|
A | C | 288 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(285): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.5423+650A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121162921 | ||||||
chr9:121163165
|
C | A | 191 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(188): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.5423+894C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163165 | ||||||
chr9:121163177
|
C | CA | 52 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(49): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.5423+919dupA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr9 | 121163177 | |||||
chr9:121163177
|
CA | C | 81 | a0002c0002t0001g0100a0003c0003t0001g0004a0003c0003t0001g0018others(78): Show | 87 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.5423+919delA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr9 | 121163177 | |||||
chr9:121163188
|
A | AT | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.5423+917_5423+918i others(3): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163188 | ||||||
chr9:121163190
|
AT | A | 106 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(103): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.5423+920delT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163190 | ||||||
chr9:121163191
|
T | A | 9 | a0002c0002t0001g0075a0002c0006t0001g0029a0002c0006t0001g0032others(6): Show | 10 | HG02451.hp1 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.5423+920T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163191 | ||||||
chr9:121163259
|
G | A | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.5423+988G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163259 | ||||||
chr9:121163319
|
CA | C | 181 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(178): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.5423+1058delA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr9 | 121163319 | |||||
chr9:121163326
|
A | AAT | 6 | a0001c0005t0001g0003a0001c0005t0001g0166a0001c0005t0001g0181others(3): Show | 8 | HG00280.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.5423+1056_5423+105 others(6): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr9 | 121163326 | |||||
chr9:121163326
|
A | AT | 5 | a0005c0008t0001g0077a0008c0012t0002g0142a0008c0012t0002g0143others(2): Show | 5 | HG01981.hp2 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.5423+1055_5423+105 others(5): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163326 | ||||||
chr9:121163326
|
A | T | 2 | a0001c0001t0001g0179a0002c0002t0001g0067 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.5423+1055A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163326 | ||||||
chr9:121163328
|
A | T | 156 | a0001c0001t0001g0011a0001c0001t0001g0149a0001c0001t0001g0150others(153): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.5423+1057A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163328 | ||||||
chr9:121163329
|
AT | A | 65 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(62): Show | 71 | HG00597.hp2 HG00639.hp2 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.5423+1059delT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163329 | ||||||
chr9:121163332
|
T | A | 1 | a0003c0003t0001g0266 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5423+1061T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163332 | ||||||
chr9:121163604
|
A | G | 13 | a0003c0004t0002g0009a0003c0004t0002g0124a0003c0004t0002g0125others(10): Show | 14 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.5423+1333A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163604 | ||||||
chr9:121163759
|
C | A | 1 | a0002c0002t0001g0022 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.5424-1184C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163759 | ||||||
chr9:121163865
|
C | CT | 168 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(165): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.5424-1061dupT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr9 | 121163865 | |||||
chr9:121163865
|
C | CTT | 7 | a0002c0002t0001g0035a0002c0002t0001g0081a0002c0002t0001g0112others(4): Show | 7 | HG01361.hp2 NA18944.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.5424-1062_5424-106 others(6): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr9 | 121163865 | |||||
chr9:121163865
|
CT | C | 57 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(54): Show | 60 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.5424-1061delT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr9 | 121163865 | |||||
chr9:121163911
|
C | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.5424-1032C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163911 | ||||||
chr9:121163931
|
C | A | 14 | a0003c0003t0001g0116a0003c0003t0001g0117a0003c0003t0001g0250others(11): Show | 14 | HG00140.hp2 HG00741.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.5424-1012C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163931 | ||||||
chr9:121163965
|
C | T | 67 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(64): Show | 72 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.5424-978C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121163965 | ||||||
chr9:121164099
|
C | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.5424-844C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121164099 | ||||||
chr9:121164115
|
C | T | 104 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(101): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.5424-828C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121164115 | ||||||
chr9:121164178
|
T | C | 4 | a0003c0004t0002g0130a0003c0004t0002g0131a0003c0019t0002g0127others(1): Show | 4 | HG00099.hp2 NA18948.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.5424-765T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121164178 | ||||||
chr9:121164260
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5424-683C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121164260 | ||||||
chr9:121164299
|
A | G | 1 | a0003c0003t0001g0266 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5424-644A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121164299 | ||||||
chr9:121164524
|
G | A | 1 | a0003c0003t0001g0270 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5424-419G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121164524 | ||||||
chr9:121164559
|
A | C | 252 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(249): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.5424-384A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121164559 | ||||||
chr9:121164585
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0206 | 3 | NA18980.hp2 NA18993.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.5424-358C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121164585 | ||||||
chr9:121164652
|
T | C | 190 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(187): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.5424-291T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | chr9 | 121164652 | ||||||
chr9:121164701
|
TATCCATG others(6): Show |
T | 3 | a0008c0012t0002g0142a0008c0012t0002g0143a0008c0012t0002g0144 | 3 | HG02976.hp1 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5424-234_5424-222d others(15): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 34/43 | INFO_REALIGN_3_PRIME | chr9 | 121164701 | |||||
chr9:121165199
|
T | A | 190 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(187): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.5581+99T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 35/43 | chr9 | 121165199 | ||||||
chr9:121165269
|
A | G | 19 | a0003c0004t0001g0140a0003c0004t0002g0009a0003c0004t0002g0123others(16): Show | 20 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.5581+169A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 35/43 | chr9 | 121165269 | ||||||
chr9:121165318
|
TA | T | 171 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(168): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.5581+229delA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 35/43 | INFO_REALIGN_3_PRIME | chr9 | 121165318 | |||||
chr9:121165412
|
C | G | 2 | a0002c0006t0001g0029a0002c0006t0001g0032 | 2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.5581+312C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 35/43 | chr9 | 121165412 | ||||||
chr9:121165687
|
C | A | 1 | a0004c0026t0001g0135 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5582-420C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 35/43 | chr9 | 121165687 | ||||||
chr9:121165881
|
C | T | 1 | a0003c0004t0002g0123 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5582-226C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 35/43 | chr9 | 121165881 | ||||||
chr9:121166064
|
A | G | 4 | a0003c0003t0001g0020a0003c0003t0001g0269a0003c0003t0001g0270others(1): Show | 5 | HG01123.hp2 HG01346.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.5582-43A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 35/43 | chr9 | 121166064 | ||||||
chr9:121166208
|
T | C | 190 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(187): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.5655+28T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 36/43 | chr9 | 121166208 | ||||||
chr9:121166291
|
G | A | 252 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(249): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.5655+111G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 36/43 | chr9 | 121166291 | ||||||
chr9:121166602
|
A | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5655+422A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 36/43 | chr9 | 121166602 | ||||||
chr9:121166686
|
A | G | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.5655+506A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 36/43 | chr9 | 121166686 | ||||||
chr9:121166862
|
A | G | 1 | a0001c0001t0001g0173 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.5656-627A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 36/43 | chr9 | 121166862 | ||||||
chr9:121166882
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0189 | 3 | HG01167.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.5656-607G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 36/43 | chr9 | 121166882 | ||||||
chr9:121167021
|
C | CA | 233 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(230): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.5656-455dupA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 36/43 | INFO_REALIGN_3_PRIME | chr9 | 121167021 | |||||
chr9:121167306
|
C | CA | 182 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(179): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.5656-171dupA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 36/43 | INFO_REALIGN_3_PRIME | chr9 | 121167306 | |||||
chr9:121167306
|
C | CAA | 72 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(69): Show | 77 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.5656-172_5656-171d others(4): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 36/43 | INFO_REALIGN_3_PRIME | chr9 | 121167306 | |||||
chr9:121167408
|
T | G | 13 | a0003c0004t0002g0009a0003c0004t0002g0123a0003c0004t0002g0124others(10): Show | 14 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.5656-81T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 36/43 | chr9 | 121167408 | ||||||
chr9:121167432
|
A | G | 248 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(245): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.5656-57A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 36/43 | chr9 | 121167432 | ||||||
chr9:121167726
|
G | A | 3 | a0008c0012t0002g0142a0008c0012t0002g0143a0008c0012t0002g0144 | 3 | HG02976.hp1 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.5844+49G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 37/43 | chr9 | 121167726 | ||||||
chr9:121167744
|
T | A | 1 | a0002c0002t0001g0064 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5844+67T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 37/43 | chr9 | 121167744 | ||||||
chr9:121168018
|
A | C | 192 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(189): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.5845-78A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 37/43 | chr9 | 121168018 | ||||||
chr9:121168080
|
A | G | 1 | a0003c0004t0001g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.5845-16A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 37/43 | chr9 | 121168080 | ||||||
chr9:121168687
|
T | C | 238 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(235): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.6070+366T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 38/43 | chr9 | 121168687 | ||||||
chr9:121168894
|
G | A | 1 | a0002c0002t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.6070+573G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 38/43 | chr9 | 121168894 | ||||||
chr9:121169136
|
T | C | 3 | a0002c0002t0001g0008a0002c0002t0001g0112a0002c0002t0001g0113 | 4 | NA19010.hp1 NA19058.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.6071-475T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 38/43 | chr9 | 121169136 | ||||||
chr9:121169249
|
T | G | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.6071-362T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 38/43 | chr9 | 121169249 | ||||||
chr9:121169600
|
G | A | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.6071-11G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 38/43 | chr9 | 121169600 | ||||||
chr9:121170011
|
A | G | 1 | a0002c0002t0001g0107 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.6276+195A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170011 | ||||||
chr9:121170018
|
T | C | 1 | a0013c0021t0001g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6276+202T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170018 | ||||||
chr9:121170184
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.6276+368T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170184 | ||||||
chr9:121170204
|
C | T | 1 | a0002c0002t0001g0036 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.6276+388C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170204 | ||||||
chr9:121170205
|
G | A | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.6276+389G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170205 | ||||||
chr9:121170205
|
G | C | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.6276+389G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170205 | ||||||
chr9:121170246
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.6276+430C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170246 | ||||||
chr9:121170407
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.6276+591G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170407 | ||||||
chr9:121170444
|
C | T | 93 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(90): Show | 98 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.6276+628C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170444 | ||||||
chr9:121170484
|
C | T | 104 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(101): Show | 109 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.6276+668C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170484 | ||||||
chr9:121170645
|
G | A | 1 | a0003c0003t0001g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6277-763G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170645 | ||||||
chr9:121170743
|
G | A | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.6277-665G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170743 | ||||||
chr9:121170828
|
T | G | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.6277-580T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170828 | ||||||
chr9:121170838
|
A | G | 31 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(28): Show | 33 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.6277-570A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170838 | ||||||
chr9:121170974
|
A | C | 1 | a0001c0001t0001g0171 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.6277-434A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121170974 | ||||||
chr9:121171049
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.6277-359C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121171049 | ||||||
chr9:121171146
|
T | A | 51 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(48): Show | 56 | HG00597.hp2 HG01081.hp1 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.6277-262T>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121171146 | ||||||
chr9:121171167
|
T | C | 1 | a0003c0003t0001g0296 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.6277-241T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121171167 | ||||||
chr9:121171228
|
T | C | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.6277-180T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121171228 | ||||||
chr9:121171268
|
G | A | 1 | a0026c0033t0001g0170 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.6277-140G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121171268 | ||||||
chr9:121171355
|
A | C | 1 | a0021c0030t0001g0235 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.6277-53A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 39/43 | chr9 | 121171355 | ||||||
chr9:121171849
|
T | G | 7 | a0001c0005t0001g0003a0001c0005t0001g0166a0001c0005t0001g0181others(4): Show | 9 | HG00280.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.6417+301T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121171849 | ||||||
chr9:121171936
|
A | G | 66 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(63): Show | 71 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.6417+388A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121171936 | ||||||
chr9:121171942
|
C | T | 6 | a0004c0007t0001g0010a0004c0007t0001g0136a0004c0007t0001g0137others(3): Show | 7 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.6417+394C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121171942 | ||||||
chr9:121172095
|
G | A | 73 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(70): Show | 79 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.6417+547G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121172095 | ||||||
chr9:121172100
|
C | T | 1 | a0003c0004t0002g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6417+552C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121172100 | ||||||
chr9:121172185
|
C | T | 228 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(225): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.6417+637C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121172185 | ||||||
chr9:121172217
|
T | C | 1 | a0003c0004t0002g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.6417+669T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121172217 | ||||||
chr9:121172263
|
A | G | 1 | a0003c0004t0002g0145 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6417+715A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121172263 | ||||||
chr9:121172368
|
C | T | 1 | a0003c0003t0001g0261 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.6417+820C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121172368 | ||||||
chr9:121172386
|
AT | A | 67 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(64): Show | 72 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.6417+839delT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121172386 | ||||||
chr9:121172456
|
C | T | 1 | a0003c0004t0002g0134 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.6418-787C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121172456 | ||||||
chr9:121172545
|
G | T | 1 | a0002c0023t0001g0092 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.6418-698G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121172545 | ||||||
chr9:121172644
|
AAAAAC | A | 6 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(3): Show | 6 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.6418-584_6418-580d others(7): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | INFO_REALIGN_3_PRIME | chr9 | 121172644 | |||||
chr9:121172727
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0189 | 3 | HG01167.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.6418-516A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121172727 | ||||||
chr9:121172944
|
T | C | 12 | a0002c0006t0001g0023a0002c0006t0001g0024a0002c0006t0001g0025others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.6418-299T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121172944 | ||||||
chr9:121172976
|
T | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG01261.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.6418-267T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121172976 | ||||||
chr9:121173234
|
A | C | 1 | a0001c0001t0001g0196 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.6418-9A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 40/43 | chr9 | 121173234 | ||||||
chr9:121173540
|
C | T | 4 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG02015.hp2 HG02040.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.6684+31C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 41/43 | chr9 | 121173540 | ||||||
chr9:121173587
|
G | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0189 | 3 | HG01167.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.6684+78G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 41/43 | chr9 | 121173587 | ||||||
chr9:121173661
|
T | C | 1 | a0019c0016t0002g0021 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.6685-14T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 41/43 | chr9 | 121173661 | ||||||
chr9:121173932
|
C | CT | 5 | a0003c0004t0002g0141a0003c0004t0002g0145a0008c0012t0002g0142others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.6747+197dupT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 42/43 | INFO_REALIGN_3_PRIME | chr9 | 121173932 | |||||
chr9:121173993
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.6747+256C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 42/43 | chr9 | 121173993 | ||||||
chr9:121174051
|
A | T | 172 | a0001c0001t0001g0194a0002c0002t0001g0001a0002c0002t0001g0005others(169): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.6747+314A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 42/43 | chr9 | 121174051 | ||||||
chr9:121174103
|
A | C | 1 | a0004c0026t0001g0135 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.6747+366A>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 42/43 | chr9 | 121174103 | ||||||
chr9:121174216
|
T | C | 194 | a0001c0001t0001g0194a0002c0002t0001g0001a0002c0002t0001g0005others(191): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.6747+479T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 42/43 | chr9 | 121174216 | ||||||
chr9:121174316
|
G | A | 172 | a0001c0001t0001g0194a0002c0002t0001g0001a0002c0002t0001g0005others(169): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.6747+579G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 42/43 | chr9 | 121174316 | ||||||
chr9:121174531
|
C | T | 2 | a0002c0006t0001g0025a0002c0006t0001g0026 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.6748-487C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 42/43 | chr9 | 121174531 | ||||||
chr9:121174613
|
C | A | 66 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(63): Show | 71 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.6748-405C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 42/43 | chr9 | 121174613 | ||||||
chr9:121174813
|
C | T | 2 | a0001c0001t0003g0239a0001c0001t0003g0241 | 2 | HG01109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.6748-205C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 42/43 | chr9 | 121174813 | ||||||
chr9:121174878
|
A | G | 56 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(53): Show | 58 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.6748-140A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 42/43 | chr9 | 121174878 | ||||||
chr9:121174962
|
G | A | 13 | a0003c0004t0002g0009a0003c0004t0002g0124a0003c0004t0002g0125others(10): Show | 14 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.6748-56G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 42/43 | chr9 | 121174962 | ||||||
chr9:121175323
|
T | C | 106 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(103): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.6954+99T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121175323 | ||||||
chr9:121175340
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.6954+116C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121175340 | ||||||
chr9:121175506
|
C | T | 1 | a0003c0003t0001g0294 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.6954+282C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121175506 | ||||||
chr9:121175531
|
A | T | 1 | a0002c0002t0001g0042 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.6954+307A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121175531 | ||||||
chr9:121175561
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.6954+337G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121175561 | ||||||
chr9:121175613
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.6954+389T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121175613 | ||||||
chr9:121175624
|
C | T | 1 | a0003c0004t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.6954+400C>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121175624 | ||||||
chr9:121175689
|
A | G | 31 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0194others(28): Show | 33 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.6954+465A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121175689 | ||||||
chr9:121175977
|
G | A | 67 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(64): Show | 72 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.6954+753G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121175977 | ||||||
chr9:121176226
|
T | C | 10 | a0002c0002t0001g0049a0002c0002t0001g0074a0002c0002t0001g0075others(7): Show | 10 | NA18942.hp2 NA18950.hp1 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.6955-937T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176226 | ||||||
chr9:121176375
|
AATTAGCA others(8): Show |
A | 1 | a0002c0002t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.6955-770_6955-756d others(17): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | INFO_REALIGN_3_PRIME | chr9 | 121176375 | |||||
chr9:121176490
|
C | A | 1 | a0002c0002t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6955-673C>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176490 | ||||||
chr9:121176494
|
G | C | 1 | a0002c0002t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6955-669G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176494 | ||||||
chr9:121176496
|
G | C | 1 | a0002c0002t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6955-667G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176496 | ||||||
chr9:121176497
|
G | C | 1 | a0002c0002t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6955-666G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176497 | ||||||
chr9:121176499
|
G | C | 1 | a0002c0002t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6955-664G>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176499 | ||||||
chr9:121176500
|
T | G | 1 | a0002c0002t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6955-663T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176500 | ||||||
chr9:121176505
|
G | A | 1 | a0002c0002t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6955-658G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176505 | ||||||
chr9:121176546
|
A | T | 1 | a0002c0002t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6955-617A>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176546 | ||||||
chr9:121176577
|
A | G | 1 | a0002c0002t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6955-586A>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176577 | ||||||
chr9:121176605
|
CCAGCTCA others(4): Show |
C | 1 | a0002c0002t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.6955-557_6955-547d others(13): Show |
CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176605 | ||||||
chr9:121176618
|
G | A | 1 | a0003c0004t0002g0129 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.6955-545G>A | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176618 | ||||||
chr9:121176681
|
T | G | 1 | a0001c0001t0001g0247 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.6955-482T>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176681 | ||||||
chr9:121176702
|
G | T | 1 | a0023c0029t0001g0224 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.6955-461G>T | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176702 | ||||||
chr9:121176720
|
T | C | 72 | a0003c0003t0001g0004a0003c0003t0001g0018a0003c0003t0001g0019others(69): Show | 77 | HG00140.hp2 HG00597.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.6955-443T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121176720 | ||||||
chr9:121176932
|
A | AT | 193 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(190): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.6955-222dupT | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | INFO_REALIGN_3_PRIME | chr9 | 121176932 | |||||
chr9:121177047
|
T | C | 8 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.6955-116T>C | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121177047 | ||||||
chr9:121177058
|
T | TA | 94 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(91): Show | 99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.6955-104dupA | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | INFO_REALIGN_3_PRIME | chr9 | 121177058 | |||||
chr9:121177078
|
C | G | 1 | a0003c0003t0001g0251 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.6955-85C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121177078 | ||||||
chr9:121177119
|
C | G | 1 | a0003c0003t0001g0266 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6955-44C>G | CNTRL | ENSG00000119397.19 | transcript | ENST00000373855.7 | protein_coding | 43/43 | chr9 | 121177119 |