geneid | 54825 |
---|---|
ensemblid | ENSG00000074276.11 |
hgncid | 18231 |
symbol | CDHR2 |
name | cadherin related family member 2 |
refseq_nuc | NM_017675.6 |
refseq_prot | NP_060145.3 |
ensembl_nuc | ENST00000261944.10 |
ensembl_prot | ENSP00000261944.5 |
mane_status | MANE Select |
chr | chr5 |
start | 176549342 |
end | 176595824 |
strand | + |
ver | v1.2 |
region | chr5:176549342-176595824 |
region5000 | chr5:176544342-176600824 |
regionname0 | CDHR2_chr5_176549342_176595824 |
regionname5000 | CDHR2_chr5_176544342_176600824 |
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 | 0/1 | 1310 | 110 | 32 | 30 | 28 | 7 | 12 | 22 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0002 | 0/0 | 1310 | 92 | 19 | 16 | 42 | 5 | 10 | 33 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003 | 0/0 | 1310 | 83 | 1 | 16 | 48 | 3 | 15 | 37 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0004 | 1/0 | 1310 | 13 | 11 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0005 | 0/0 | 1310 | 7 | 2 | 0 | 0 | 2 | 3 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0006 | 0/0 | 1310 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0007 | 0/0 | 1310 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0008 | 0/0 | 1310 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0009 | 0/0 | 1310 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0010 | 0/0 | 1310 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0011 | 0/0 | 1310 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0012 | 0/0 | 1310 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0013 | 0/0 | 1310 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0014 | 0/0 | 1310 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0015 | 0/0 | 1310 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0016 | 0/0 | 1310 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0017 | 0/0 | 1310 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0018 | 0/0 | 1310 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0019 | 0/0 | 1310 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0020 | 0/0 | 1310 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0021 | 0/0 | 1310 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0022 | 0/0 | 1310 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0023 | 0/0 | 1310 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
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 | 0/0 | 3933 | 84 | 16 | 15 | 38 | 5 | 10 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0002 | 0/0 | 3933 | 72 | 1 | 12 | 43 | 3 | 13 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0003 | 0/1 | 3933 | 39 | 4 | 21 | 1 | 5 | 7 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0004 | 0/0 | 3933 | 31 | 4 | 3 | 18 | 1 | 5 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0005 | 0/0 | 3933 | 9 | 6 | 2 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0006 | 0/0 | 3933 | 8 | 2 | 1 | 5 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0007 | 0/0 | 3933 | 7 | 2 | 0 | 0 | 2 | 3 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0008 | 0/0 | 3933 | 5 | 5 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0009 | 1/0 | 3933 | 5 | 4 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0010 | 0/0 | 3933 | 5 | 5 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0011 | 0/0 | 3933 | 4 | 3 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0012 | 0/0 | 3933 | 4 | 0 | 2 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0013 | 0/0 | 3933 | 4 | 1 | 3 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0014 | 0/0 | 3933 | 3 | 3 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0015 | 0/0 | 3933 | 3 | 0 | 3 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0016 | 0/0 | 3933 | 3 | 3 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0017 | 0/0 | 3933 | 3 | 3 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0018 | 0/0 | 3933 | 3 | 0 | 3 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0019 | 0/0 | 3933 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0020 | 0/0 | 3933 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0021 | 0/0 | 3933 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0022 | 0/0 | 3933 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0023 | 0/0 | 3933 | 2 | 1 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0024 | 0/0 | 3933 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0025 | 0/0 | 3933 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0026 | 0/0 | 3933 | 2 | 0 | 1 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0027 | 0/0 | 3933 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0028 | 0/0 | 3933 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0029 | 0/0 | 3933 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0030 | 0/0 | 3933 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0031 | 0/0 | 3933 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0032 | 0/0 | 3933 | 2 | 0 | 0 | 0 | 0 | 2 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0033 | 0/0 | 3933 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0034 | 0/0 | 3933 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0035 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0036 | 0/0 | 3933 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0037 | 0/0 | 3933 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0038 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0039 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0040 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0041 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0042 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0043 | 0/0 | 3933 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0044 | 0/0 | 3933 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0045 | 0/0 | 3933 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0046 | 0/0 | 3933 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0047 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0048 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0049 | 0/0 | 3933 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0050 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0051 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0052 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0053 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0054 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
c0055 | 0/0 | 3933 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
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 | 241 | 342 | 90 | 70 | 124 | 18 | 38 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
t0002 | 0/0 | 241 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
t0003 | 0/0 | 241 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
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 | 4 | 0 | 0 | 4 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0005 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0007 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0003 | 0/1 | 3933 | 39 | 4 | 21 | 1 | 5 | 7 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0004 | 0/0 | 3933 | 31 | 4 | 3 | 18 | 1 | 5 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0005 | 0/0 | 3933 | 9 | 6 | 2 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0006 | 0/0 | 3933 | 8 | 2 | 1 | 5 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0008 | 0/0 | 3933 | 5 | 5 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0013 | 0/0 | 3933 | 4 | 1 | 3 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0016 | 0/0 | 3933 | 3 | 3 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0017 | 0/0 | 3933 | 3 | 3 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0025 | 0/0 | 3933 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0038 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0041 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0044 | 0/0 | 3933 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0046 | 0/0 | 3933 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0047 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0048 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0002c0001 | 0/0 | 3933 | 84 | 16 | 15 | 38 | 5 | 10 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0002c0023 | 0/0 | 3933 | 2 | 1 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0002c0026 | 0/0 | 3933 | 2 | 0 | 1 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0002c0030 | 0/0 | 3933 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0002c0052 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0002c0053 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003c0002 | 0/0 | 3933 | 72 | 1 | 12 | 43 | 3 | 13 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003c0012 | 0/0 | 3933 | 4 | 0 | 2 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003c0032 | 0/0 | 3933 | 2 | 0 | 0 | 0 | 0 | 2 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003c0033 | 0/0 | 3933 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003c0036 | 0/0 | 3933 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003c0037 | 0/0 | 3933 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003c0045 | 0/0 | 3933 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0004c0009 | 1/0 | 3933 | 5 | 4 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0004c0010 | 0/0 | 3933 | 5 | 5 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0004c0039 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0004c0042 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0004c0055 | 0/0 | 3933 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0005c0007 | 0/0 | 3933 | 7 | 2 | 0 | 0 | 2 | 3 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0006c0014 | 0/0 | 3933 | 3 | 3 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0006c0019 | 0/0 | 3933 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0007c0027 | 0/0 | 3933 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0007c0031 | 0/0 | 3933 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0007c0050 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0008c0011 | 0/0 | 3933 | 4 | 3 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0009c0015 | 0/0 | 3933 | 3 | 0 | 3 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0010c0018 | 0/0 | 3933 | 3 | 0 | 3 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0011c0028 | 0/0 | 3933 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0012c0021 | 0/0 | 3933 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0013c0022 | 0/0 | 3933 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0014c0020 | 0/0 | 3933 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0015c0024 | 0/0 | 3933 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0016c0029 | 0/0 | 3933 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0017c0040 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0018c0035 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0019c0043 | 0/0 | 3933 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0020c0051 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0021c0049 | 0/0 | 3933 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0022c0054 | 0/0 | 3933 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0023c0034 | 0/0 | 3933 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0003t0001 | 0/1 | 4173 | 38 | 4 | 21 | 1 | 5 | 6 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0003t0003 | 0/0 | 4173 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0004t0001 | 0/0 | 4173 | 30 | 4 | 3 | 18 | 1 | 4 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0004t0002 | 0/0 | 4173 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0005t0001 | 0/0 | 4173 | 9 | 6 | 2 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0006t0001 | 0/0 | 4173 | 8 | 2 | 1 | 5 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0008t0001 | 0/0 | 4173 | 5 | 5 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0013t0001 | 0/0 | 4173 | 4 | 1 | 3 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0016t0001 | 0/0 | 4173 | 3 | 3 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0017t0001 | 0/0 | 4173 | 3 | 3 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0025t0001 | 0/0 | 4173 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0038t0001 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0041t0001 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0044t0001 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0046t0001 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0047t0001 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0001c0048t0001 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0002c0001t0001 | 0/0 | 4173 | 84 | 16 | 15 | 38 | 5 | 10 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0002c0023t0001 | 0/0 | 4173 | 2 | 1 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0002c0026t0001 | 0/0 | 4173 | 2 | 0 | 1 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0002c0030t0001 | 0/0 | 4173 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0002c0052t0001 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0002c0053t0001 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003c0002t0001 | 0/0 | 4173 | 72 | 1 | 12 | 43 | 3 | 13 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003c0012t0001 | 0/0 | 4173 | 4 | 0 | 2 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003c0032t0001 | 0/0 | 4173 | 2 | 0 | 0 | 0 | 0 | 2 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003c0033t0001 | 0/0 | 4173 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003c0036t0001 | 0/0 | 4173 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003c0037t0001 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0003c0045t0001 | 0/0 | 4173 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0004c0009t0001 | 1/0 | 4173 | 5 | 4 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0004c0010t0001 | 0/0 | 4173 | 5 | 5 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0004c0039t0001 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0004c0042t0001 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0004c0055t0001 | 0/0 | 4173 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0005c0007t0001 | 0/0 | 4173 | 7 | 2 | 0 | 0 | 2 | 3 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0006c0014t0001 | 0/0 | 4173 | 3 | 3 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0006c0019t0001 | 0/0 | 4173 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0007c0027t0001 | 0/0 | 4173 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0007c0031t0001 | 0/0 | 4173 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0007c0050t0001 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0008c0011t0001 | 0/0 | 4173 | 4 | 3 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0009c0015t0001 | 0/0 | 4173 | 3 | 0 | 3 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0010c0018t0001 | 0/0 | 4173 | 3 | 0 | 3 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0011c0028t0001 | 0/0 | 4173 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0012c0021t0001 | 0/0 | 4173 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0013c0022t0001 | 0/0 | 4173 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0014c0020t0001 | 0/0 | 4173 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0015c0024t0001 | 0/0 | 4173 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0016c0029t0001 | 0/0 | 4173 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0017c0040t0001 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0018c0035t0001 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0019c0043t0001 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0020c0051t0001 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0021c0049t0001 | 0/0 | 4173 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0022c0054t0001 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
a0023c0034t0001 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | copy fasta | chr5 | 176544342 | 176600824 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0003t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0004t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0005t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0005t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0005t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0005t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0005t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0005t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0005t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0006t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0006t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0006t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0006t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0006t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0006t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0006t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0008t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0008t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0008t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0008t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0008t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0013t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0013t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0016t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0016t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0017t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0017t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0017t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0025t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0025t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0038t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0041t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0044t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0046t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0047t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0001c0048t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0005 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0023t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0023t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0026t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0026t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0030t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0030t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0052t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0002c0053t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0012t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0012t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0012t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0012t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0032t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0032t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0033t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0033t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0036t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0037t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0003c0045t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0004c0009t0001g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0004c0009t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0004c0009t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0004c0009t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0004c0009t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0004c0010t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0004c0010t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0004c0010t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0004c0039t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0004c0042t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0004c0055t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0005c0007t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0005c0007t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0005c0007t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0005c0007t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0005c0007t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0005c0007t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0006c0014t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0006c0014t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0006c0019t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0006c0019t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0007c0027t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0007c0027t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0007c0031t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0007c0031t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0007c0050t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0008c0011t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0008c0011t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0008c0011t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0008c0011t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0009c0015t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0009c0015t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0009c0015t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0010c0018t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0010c0018t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0011c0028t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0011c0028t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0012c0021t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0012c0021t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0013c0022t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0013c0022t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0014c0020t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0014c0020t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0015c0024t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0015c0024t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0016c0029t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0016c0029t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0017c0040t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0018c0035t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0019c0043t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0020c0051t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0021c0049t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0022c0054t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
a0023c0034t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0001 | g0064 | EUR | GBR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00099 | hp2 | a0002 | c0001 | t0001 | g0154 | EUR | GBR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00140 | hp1 | a0001 | c0005 | t0001 | g0200 | EUR | GBR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00140 | hp2 | a0002 | c0001 | t0001 | g0089 | EUR | GBR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00280 | hp1 | a0001 | c0004 | t0001 | g0278 | EUR | FIN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00280 | hp2 | a0005 | c0007 | t0001 | g0062 | EUR | FIN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00323 | hp1 | a0003 | c0002 | t0001 | g0219 | EUR | FIN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0101 | EUR | FIN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00408 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00408 | hp2 | a0003 | c0002 | t0001 | g0209 | EAS | CHS | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00423 | hp1 | a0001 | c0046 | t0001 | g0297 | EAS | CHS | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00423 | hp2 | a0003 | c0002 | t0001 | g0215 | EAS | CHS | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00438 | hp1 | a0002 | c0001 | t0001 | g0060 | EAS | CHS | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00438 | hp2 | a0002 | c0001 | t0001 | g0093 | EAS | CHS | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00639 | hp1 | a0002 | c0001 | t0001 | g0080 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00639 | hp2 | a0003 | c0002 | t0001 | g0212 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00642 | hp1 | a0010 | c0018 | t0001 | g0004 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0306 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00733 | hp1 | a0003 | c0012 | t0001 | g0086 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00733 | hp2 | a0008 | c0011 | t0001 | g0172 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0310 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00735 | hp2 | a0002 | c0001 | t0001 | g0015 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0309 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00738 | hp2 | a0003 | c0002 | t0001 | g0298 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0307 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG00741 | hp2 | a0002 | c0001 | t0001 | g0091 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01069 | hp1 | a0010 | c0018 | t0001 | g0057 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01069 | hp2 | a0001 | c0013 | t0001 | g0002 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01070 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01070 | hp2 | a0001 | c0013 | t0001 | g0002 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01071 | hp1 | a0010 | c0018 | t0001 | g0004 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01071 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01074 | hp1 | a0001 | c0013 | t0001 | g0002 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01074 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01081 | hp1 | a0001 | c0004 | t0001 | g0040 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01081 | hp2 | a0002 | c0001 | t0001 | g0077 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01106 | hp1 | a0003 | c0002 | t0001 | g0246 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01109 | hp1 | a0004 | c0055 | t0001 | g0033 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0257 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01167 | hp1 | a0001 | c0005 | t0001 | g0018 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01167 | hp2 | a0002 | c0001 | t0001 | g0132 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01168 | hp1 | a0003 | c0045 | t0001 | g0041 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01168 | hp2 | a0002 | c0001 | t0001 | g0015 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01169 | hp1 | a0001 | c0005 | t0001 | g0018 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01169 | hp2 | a0002 | c0001 | t0001 | g0148 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01175 | hp1 | a0001 | c0003 | t0001 | g0100 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01175 | hp2 | a0002 | c0001 | t0001 | g0070 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01192 | hp1 | a0003 | c0002 | t0001 | g0188 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0122 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01243 | hp1 | a0002 | c0001 | t0001 | g0050 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0099 | AMR | PUR | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01255 | hp1 | a0001 | c0004 | t0001 | g0279 | AMR | CLM | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0256 | AMR | CLM | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01256 | hp1 | a0003 | c0002 | t0001 | g0237 | AMR | CLM | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01256 | hp2 | a0002 | c0001 | t0001 | g0108 | AMR | CLM | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01258 | hp1 | a0002 | c0001 | t0001 | g0069 | AMR | CLM | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0010 | AMR | CLM | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01361 | hp1 | a0001 | c0003 | t0001 | g0301 | AMR | CLM | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01361 | hp2 | a0002 | c0001 | t0001 | g0149 | AMR | CLM | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01433 | hp1 | a0003 | c0002 | t0001 | g0204 | AMR | CLM | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01433 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | CLM | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0304 | AMR | CLM | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0047 | AMR | CLM | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01515 | hp1 | a0021 | c0049 | t0001 | g0054 | EUR | IBS | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01515 | hp2 | a0001 | c0003 | t0001 | g0023 | EUR | IBS | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01516 | hp1 | a0002 | c0001 | t0001 | g0007 | EUR | IBS | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01516 | hp2 | a0003 | c0002 | t0001 | g0189 | EUR | IBS | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01517 | hp1 | a0001 | c0003 | t0001 | g0023 | EUR | IBS | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01517 | hp2 | a0003 | c0002 | t0001 | g0191 | EUR | IBS | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01884 | hp1 | a0006 | c0019 | t0001 | g0043 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0169 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01891 | hp1 | a0004 | c0009 | t0001 | g0147 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01891 | hp2 | a0001 | c0048 | t0001 | g0315 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01928 | hp1 | a0001 | c0006 | t0001 | g0117 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01928 | hp2 | a0001 | c0003 | t0001 | g0107 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01934 | hp1 | a0003 | c0002 | t0001 | g0106 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01934 | hp2 | a0003 | c0002 | t0001 | g0072 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01952 | hp1 | a0003 | c0002 | t0001 | g0239 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01952 | hp2 | a0002 | c0026 | t0001 | g0201 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01975 | hp1 | a0001 | c0004 | t0001 | g0271 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01975 | hp2 | a0009 | c0015 | t0001 | g0193 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01978 | hp1 | a0003 | c0002 | t0001 | g0020 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0098 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01981 | hp1 | a0003 | c0002 | t0001 | g0240 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01981 | hp2 | a0003 | c0036 | t0001 | g0223 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01993 | hp1 | a0009 | c0015 | t0001 | g0227 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG01993 | hp2 | a0002 | c0001 | t0001 | g0095 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02027 | hp1 | a0003 | c0002 | t0001 | g0019 | EAS | KHV | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02027 | hp2 | a0002 | c0001 | t0001 | g0235 | EAS | KHV | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02040 | hp1 | a0002 | c0001 | t0001 | g0007 | EAS | KHV | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02040 | hp2 | a0003 | c0002 | t0001 | g0205 | EAS | KHV | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02055 | hp1 | a0007 | c0050 | t0001 | g0136 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02055 | hp2 | a0001 | c0047 | t0001 | g0174 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02056 | hp1 | a0003 | c0002 | t0001 | g0234 | EAS | KHV | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02056 | hp2 | a0003 | c0002 | t0001 | g0198 | EAS | KHV | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02071 | hp1 | a0003 | c0002 | t0001 | g0221 | EAS | KHV | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02071 | hp2 | a0001 | c0044 | t0001 | g0022 | EAS | KHV | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02074 | hp1 | a0002 | c0001 | t0001 | g0232 | EAS | KHV | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02074 | hp2 | a0003 | c0002 | t0001 | g0303 | EAS | KHV | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02083 | hp1 | a0003 | c0002 | t0001 | g0230 | EAS | KHV | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02083 | hp2 | a0001 | c0006 | t0001 | g0233 | EAS | KHV | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02132 | hp1 | a0001 | c0025 | t0001 | g0216 | EAS | KHV | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02132 | hp2 | a0002 | c0001 | t0001 | g0088 | EAS | KHV | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02145 | hp1 | a0004 | c0010 | t0001 | g0016 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02145 | hp2 | a0002 | c0001 | t0001 | g0034 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02148 | hp1 | a0003 | c0002 | t0001 | g0156 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02148 | hp2 | a0001 | c0003 | t0001 | g0161 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02155 | hp1 | a0001 | c0004 | t0001 | g0022 | EAS | CDX | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02155 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | CDX | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02165 | hp1 | a0002 | c0001 | t0001 | g0109 | EAS | CDX | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02165 | hp2 | a0003 | c0002 | t0001 | g0229 | EAS | CDX | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02258 | hp1 | a0002 | c0001 | t0001 | g0130 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02258 | hp2 | a0004 | c0010 | t0001 | g0017 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02280 | hp1 | a0002 | c0001 | t0001 | g0005 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02280 | hp2 | a0002 | c0023 | t0001 | g0027 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02293 | hp1 | a0003 | c0012 | t0001 | g0280 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02293 | hp2 | a0009 | c0015 | t0001 | g0225 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02300 | hp1 | a0001 | c0003 | t0001 | g0021 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02300 | hp2 | a0002 | c0001 | t0001 | g0079 | AMR | PEL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02451 | hp1 | a0001 | c0008 | t0001 | g0166 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02451 | hp2 | a0008 | c0011 | t0001 | g0313 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02572 | hp1 | a0002 | c0001 | t0001 | g0026 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02572 | hp2 | a0001 | c0041 | t0001 | g0264 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02602 | hp1 | a0002 | c0001 | t0001 | g0153 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02602 | hp2 | a0005 | c0007 | t0001 | g0097 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02615 | hp1 | a0004 | c0010 | t0001 | g0017 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02615 | hp2 | a0011 | c0028 | t0001 | g0302 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02622 | hp1 | a0006 | c0014 | t0001 | g0045 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02622 | hp2 | a0002 | c0001 | t0001 | g0030 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02630 | hp1 | a0011 | c0028 | t0001 | g0145 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02630 | hp2 | a0018 | c0035 | t0001 | g0182 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02647 | hp1 | a0001 | c0008 | t0001 | g0165 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02647 | hp2 | a0002 | c0001 | t0001 | g0129 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02683 | hp1 | a0002 | c0001 | t0001 | g0008 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02683 | hp2 | a0003 | c0032 | t0001 | g0120 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02717 | hp1 | a0001 | c0003 | t0001 | g0308 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02717 | hp2 | a0007 | c0031 | t0001 | g0317 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02723 | hp1 | a0004 | c0039 | t0001 | g0024 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02723 | hp2 | a0004 | c0009 | t0001 | g0168 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02735 | hp1 | a0002 | c0001 | t0001 | g0063 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02735 | hp2 | a0005 | c0007 | t0001 | g0065 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02738 | hp1 | a0002 | c0001 | t0001 | g0158 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0160 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02809 | hp1 | a0002 | c0001 | t0001 | g0151 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02809 | hp2 | a0012 | c0021 | t0001 | g0314 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02818 | hp1 | a0002 | c0001 | t0001 | g0052 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02818 | hp2 | a0001 | c0008 | t0001 | g0178 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02895 | hp1 | a0013 | c0022 | t0001 | g0262 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02895 | hp2 | a0002 | c0001 | t0001 | g0133 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02896 | hp1 | a0001 | c0008 | t0001 | g0177 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02896 | hp2 | a0017 | c0040 | t0001 | g0167 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02897 | hp1 | a0001 | c0008 | t0001 | g0176 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02897 | hp2 | a0013 | c0022 | t0001 | g0261 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02922 | hp1 | a0005 | c0007 | t0001 | g0138 | AFR | ESN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02922 | hp2 | a0007 | c0027 | t0001 | g0036 | AFR | ESN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02965 | hp1 | a0007 | c0031 | t0001 | g0316 | AFR | ESN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02965 | hp2 | a0001 | c0016 | t0001 | g0137 | AFR | ESN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02970 | hp1 | a0004 | c0010 | t0001 | g0032 | AFR | ESN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02970 | hp2 | a0001 | c0016 | t0001 | g0014 | AFR | ESN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02976 | hp1 | a0001 | c0017 | t0001 | g0134 | AFR | ESN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02976 | hp2 | a0001 | c0006 | t0001 | g0141 | AFR | ESN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03017 | hp1 | a0001 | c0003 | t0003 | g0105 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03017 | hp2 | a0003 | c0002 | t0001 | g0190 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03041 | hp1 | a0001 | c0004 | t0001 | g0295 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03041 | hp2 | a0006 | c0014 | t0001 | g0003 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03098 | hp1 | a0001 | c0017 | t0001 | g0135 | AFR | MSL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03098 | hp2 | a0001 | c0004 | t0001 | g0179 | AFR | MSL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03139 | hp1 | a0006 | c0019 | t0001 | g0044 | AFR | ESN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03139 | hp2 | a0001 | c0005 | t0001 | g0173 | AFR | ESN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03195 | hp1 | a0005 | c0007 | t0001 | g0139 | AFR | ESN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03195 | hp2 | a0014 | c0020 | t0001 | g0181 | AFR | ESN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03209 | hp1 | a0001 | c0006 | t0001 | g0170 | AFR | MSL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03209 | hp2 | a0006 | c0014 | t0001 | g0003 | AFR | MSL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03225 | hp1 | a0002 | c0001 | t0001 | g0025 | AFR | MSL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03225 | hp2 | a0002 | c0001 | t0001 | g0140 | AFR | MSL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03453 | hp1 | a0001 | c0005 | t0001 | g0013 | AFR | MSL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03453 | hp2 | a0008 | c0011 | t0001 | g0171 | AFR | MSL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03486 | hp1 | a0008 | c0011 | t0001 | g0277 | AFR | MSL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03486 | hp2 | a0001 | c0038 | t0001 | g0152 | AFR | MSL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03491 | hp1 | a0002 | c0001 | t0001 | g0092 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03491 | hp2 | a0003 | c0002 | t0001 | g0220 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03492 | hp1 | a0002 | c0001 | t0001 | g0008 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03492 | hp2 | a0003 | c0032 | t0001 | g0121 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03516 | hp1 | a0004 | c0010 | t0001 | g0016 | AFR | ESN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03516 | hp2 | a0007 | c0027 | t0001 | g0035 | AFR | ESN | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03540 | hp1 | a0002 | c0001 | t0001 | g0049 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03540 | hp2 | a0004 | c0042 | t0001 | g0143 | AFR | GWD | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03654 | hp1 | a0001 | c0004 | t0002 | g0276 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03654 | hp2 | a0003 | c0002 | t0001 | g0244 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03669 | hp1 | a0003 | c0002 | t0001 | g0019 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03669 | hp2 | a0003 | c0002 | t0001 | g0222 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03688 | hp1 | a0001 | c0003 | t0001 | g0039 | SAS | STU | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03688 | hp2 | a0001 | c0004 | t0001 | g0288 | SAS | STU | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03704 | hp1 | a0001 | c0004 | t0001 | g0290 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03704 | hp2 | a0003 | c0002 | t0001 | g0020 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03710 | hp1 | a0001 | c0003 | t0001 | g0061 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03710 | hp2 | a0003 | c0002 | t0001 | g0238 | SAS | PJL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03831 | hp1 | a0005 | c0007 | t0001 | g0009 | SAS | BEB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03831 | hp2 | a0001 | c0003 | t0001 | g0318 | SAS | BEB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03834 | hp1 | a0001 | c0004 | t0001 | g0287 | SAS | BEB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03834 | hp2 | a0002 | c0001 | t0001 | g0118 | SAS | BEB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03942 | hp1 | a0002 | c0001 | t0001 | g0159 | SAS | BEB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03942 | hp2 | a0003 | c0002 | t0001 | g0249 | SAS | BEB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG04115 | hp1 | a0003 | c0002 | t0001 | g0214 | SAS | STU | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG04115 | hp2 | a0003 | c0002 | t0001 | g0185 | SAS | STU | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0162 | SAS | BEB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG04184 | hp2 | a0003 | c0002 | t0001 | g0252 | SAS | BEB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG04199 | hp1 | a0003 | c0002 | t0001 | g0253 | SAS | STU | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG04199 | hp2 | a0001 | c0004 | t0001 | g0289 | SAS | STU | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG04228 | hp1 | a0002 | c0001 | t0001 | g0115 | SAS | STU | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0102 | SAS | STU | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18522 | hp1 | a0002 | c0052 | t0001 | g0155 | AFR | YRI | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18522 | hp2 | a0001 | c0016 | t0001 | g0014 | AFR | YRI | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18612 | hp1 | a0001 | c0004 | t0001 | g0270 | EAS | CHB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18612 | hp2 | a0003 | c0002 | t0001 | g0183 | EAS | CHB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18906 | hp1 | a0001 | c0017 | t0001 | g0144 | AFR | YRI | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18906 | hp2 | a0002 | c0001 | t0001 | g0028 | AFR | YRI | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18939 | hp1 | a0002 | c0001 | t0001 | g0068 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18939 | hp2 | a0001 | c0004 | t0001 | g0268 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18940 | hp1 | a0002 | c0001 | t0001 | g0114 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18940 | hp2 | a0003 | c0002 | t0001 | g0248 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18943 | hp1 | a0001 | c0006 | t0001 | g0011 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18943 | hp2 | a0001 | c0004 | t0001 | g0294 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18944 | hp1 | a0003 | c0002 | t0001 | g0236 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18944 | hp2 | a0001 | c0006 | t0001 | g0011 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18945 | hp1 | a0003 | c0002 | t0001 | g0192 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18945 | hp2 | a0002 | c0001 | t0001 | g0096 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18947 | hp1 | a0003 | c0002 | t0001 | g0263 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18947 | hp2 | a0016 | c0029 | t0001 | g0094 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18950 | hp1 | a0003 | c0002 | t0001 | g0254 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18950 | hp2 | a0003 | c0033 | t0001 | g0066 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18951 | hp1 | a0019 | c0043 | t0001 | g0281 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18951 | hp2 | a0003 | c0002 | t0001 | g0203 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18952 | hp1 | a0002 | c0001 | t0001 | g0113 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18952 | hp2 | a0003 | c0002 | t0001 | g0202 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18954 | hp1 | a0003 | c0037 | t0001 | g0211 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18954 | hp2 | a0002 | c0001 | t0001 | g0116 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18959 | hp1 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18959 | hp2 | a0003 | c0002 | t0001 | g0194 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18966 | hp1 | a0023 | c0034 | t0001 | g0251 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18966 | hp2 | a0002 | c0001 | t0001 | g0076 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18967 | hp1 | a0002 | c0001 | t0001 | g0127 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18967 | hp2 | a0003 | c0002 | t0001 | g0226 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18968 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18968 | hp2 | a0002 | c0030 | t0001 | g0269 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18969 | hp1 | a0002 | c0001 | t0001 | g0053 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18969 | hp2 | a0003 | c0002 | t0001 | g0243 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18971 | hp1 | a0003 | c0002 | t0001 | g0217 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18971 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18975 | hp1 | a0002 | c0001 | t0001 | g0125 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18975 | hp2 | a0002 | c0001 | t0001 | g0074 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18977 | hp1 | a0002 | c0001 | t0001 | g0058 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18977 | hp2 | a0003 | c0002 | t0001 | g0207 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18979 | hp1 | a0001 | c0006 | t0001 | g0110 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18979 | hp2 | a0001 | c0004 | t0001 | g0300 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18981 | hp1 | a0001 | c0004 | t0001 | g0299 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18981 | hp2 | a0002 | c0001 | t0001 | g0056 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18982 | hp1 | a0003 | c0002 | t0001 | g0184 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18982 | hp2 | a0001 | c0004 | t0001 | g0283 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18983 | hp1 | a0001 | c0025 | t0001 | g0195 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18983 | hp2 | a0003 | c0033 | t0001 | g0112 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18984 | hp1 | a0001 | c0004 | t0001 | g0266 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18984 | hp2 | a0002 | c0001 | t0001 | g0124 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18986 | hp1 | a0001 | c0004 | t0001 | g0272 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18986 | hp2 | a0003 | c0012 | t0001 | g0067 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18989 | hp1 | a0003 | c0002 | t0001 | g0213 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18989 | hp2 | a0002 | c0001 | t0001 | g0126 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18993 | hp1 | a0003 | c0002 | t0001 | g0247 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18993 | hp2 | a0002 | c0001 | t0001 | g0083 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18998 | hp1 | a0003 | c0012 | t0001 | g0085 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18998 | hp2 | a0003 | c0002 | t0001 | g0197 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18999 | hp1 | a0002 | c0001 | t0001 | g0081 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA18999 | hp2 | a0001 | c0004 | t0001 | g0260 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19001 | hp1 | a0002 | c0001 | t0001 | g0055 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19001 | hp2 | a0003 | c0002 | t0001 | g0224 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0103 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19002 | hp2 | a0003 | c0002 | t0001 | g0242 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19005 | hp1 | a0003 | c0002 | t0001 | g0208 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19005 | hp2 | a0002 | c0001 | t0001 | g0075 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19007 | hp1 | a0002 | c0001 | t0001 | g0087 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19007 | hp2 | a0002 | c0030 | t0001 | g0284 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19009 | hp1 | a0016 | c0029 | t0001 | g0275 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19009 | hp2 | a0002 | c0026 | t0001 | g0293 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19012 | hp1 | a0002 | c0001 | t0001 | g0082 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19012 | hp2 | a0001 | c0006 | t0001 | g0111 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19030 | hp1 | a0001 | c0005 | t0001 | g0296 | AFR | LWK | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19030 | hp2 | a0004 | c0009 | t0001 | g0146 | AFR | LWK | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0048 | AFR | LWK | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19043 | hp2 | a0002 | c0001 | t0001 | g0051 | AFR | LWK | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19056 | hp1 | a0001 | c0004 | t0001 | g0285 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19056 | hp2 | a0002 | c0001 | t0001 | g0078 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19067 | hp1 | a0002 | c0001 | t0001 | g0123 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19067 | hp2 | a0001 | c0004 | t0001 | g0291 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19070 | hp1 | a0001 | c0004 | t0001 | g0282 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19070 | hp2 | a0003 | c0002 | t0001 | g0186 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19074 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19074 | hp2 | a0003 | c0002 | t0001 | g0241 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19077 | hp1 | a0001 | c0004 | t0001 | g0274 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19077 | hp2 | a0003 | c0002 | t0001 | g0245 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19078 | hp1 | a0001 | c0004 | t0001 | g0059 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19078 | hp2 | a0003 | c0002 | t0001 | g0206 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19079 | hp1 | a0015 | c0024 | t0001 | g0073 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19079 | hp2 | a0003 | c0002 | t0001 | g0199 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19080 | hp1 | a0003 | c0002 | t0001 | g0231 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19080 | hp2 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19082 | hp1 | a0002 | c0001 | t0001 | g0128 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19082 | hp2 | a0003 | c0002 | t0001 | g0210 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19084 | hp1 | a0003 | c0002 | t0001 | g0187 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19084 | hp2 | a0001 | c0004 | t0001 | g0286 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19085 | hp1 | a0003 | c0002 | t0001 | g0255 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19085 | hp2 | a0003 | c0002 | t0001 | g0292 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19087 | hp1 | a0002 | c0001 | t0001 | g0157 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19087 | hp2 | a0003 | c0002 | t0001 | g0218 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19088 | hp1 | a0001 | c0004 | t0001 | g0273 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19088 | hp2 | a0003 | c0002 | t0001 | g0228 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19090 | hp1 | a0015 | c0024 | t0001 | g0071 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19090 | hp2 | a0003 | c0002 | t0001 | g0250 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19091 | hp1 | a0002 | c0023 | t0001 | g0042 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19091 | hp2 | a0001 | c0004 | t0001 | g0267 | EAS | JPT | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19240 | hp1 | a0001 | c0005 | t0001 | g0013 | AFR | YRI | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA19240 | hp2 | a0012 | c0021 | t0001 | g0037 | AFR | YRI | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA20752 | hp1 | a0005 | c0007 | t0001 | g0009 | EUR | TSI | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0258 | EUR | TSI | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA20805 | hp1 | a0001 | c0003 | t0001 | g0259 | EUR | TSI | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA20805 | hp2 | a0002 | c0001 | t0001 | g0005 | EUR | TSI | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA20905 | hp1 | a0002 | c0001 | t0001 | g0119 | SAS | GIH | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA20905 | hp2 | a0003 | c0002 | t0001 | g0196 | SAS | GIH | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02109 | hp1 | a0002 | c0001 | t0001 | g0038 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0305 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02486 | hp1 | a0001 | c0005 | t0001 | g0311 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0163 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02559 | hp1 | a0004 | c0009 | t0001 | g0312 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG02559 | hp2 | a0020 | c0051 | t0001 | g0150 | AFR | ACB | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03471 | hp1 | a0002 | c0001 | t0001 | g0142 | AFR | MSL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG03471 | hp2 | a0002 | c0053 | t0001 | g0131 | AFR | MSL | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG06807 | hp1 | a0001 | c0013 | t0001 | g0029 | AFR | USA | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
HG06807 | hp2 | a0014 | c0020 | t0001 | g0180 | AFR | USA | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA20300 | hp1 | a0003 | c0002 | t0001 | g0164 | AFR | USA | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA20300 | hp2 | a0022 | c0054 | t0001 | g0175 | AFR | USA | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA21309 | hp1 | a0001 | c0004 | t0001 | g0265 | AFR | LWK | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
NA21309 | hp2 | a0001 | c0005 | t0001 | g0046 | AFR | LWK | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0104 | REF | REF | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
homoSapiens_grch38 | hp1 | a0004 | c0009 | t0001 | g0031 | REF | REF | CDHR2_chr5_176544342_176600824 | CDHR2 | chr5 | 176544342 | 176600824 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:176568710
|
C | A | 2 | a0006a0008 | 9 | HG00733.hp2 HG01884.hp1 HG02451.hp2 others(6): Show |
missense_variant | MODERATE | c.157C>A | p.Gln53Lys | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 4/32 | 245/4173 | 157/3933 | 53/1310 | chr5 | 176568710 | ||
chr5:176571258
|
G | A | 1 | a0023 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.361G>A | p.Ala121Thr | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/32 | 449/4173 | 361/3933 | 121/1310 | chr5 | 176571258 | ||
chr5:176574099
|
G | A | 1 | a0011 | 2 | HG02615.hp2 HG02630.hp1 |
missense_variant | MODERATE | c.422G>A | p.Ser141Asn | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/32 | 510/4173 | 422/3933 | 141/1310 | chr5 | 176574099 | ||
chr5:176575294
|
G | A | 1 | a0017 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.636G>A | p.Met212Ile | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 9/32 | 724/4173 | 636/3933 | 212/1310 | chr5 | 176575294 | ||
chr5:176575733
|
G | A | 1 | a0009 | 3 | HG01975.hp2 HG01993.hp1 HG02293.hp2 |
missense_variant | MODERATE | c.854G>A | p.Arg285Gln | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 11/32 | 942/4173 | 854/3933 | 285/1310 | chr5 | 176575733 | ||
chr5:176577475
|
T | C | 19 | a0001a0002a0003others(16): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
missense_variant | MODERATE | c.1271T>C | p.Val424Ala | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 13/32 | 1359/4173 | 1271/3933 | 424/1310 | chr5 | 176577475 | ||
chr5:176577655
|
G | A | 2 | a0012a0013 | 4 | HG02809.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
missense_variant | MODERATE | c.1369G>A | p.Val457Ile | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 14/32 | 1457/4173 | 1369/3933 | 457/1310 | chr5 | 176577655 | ||
chr5:176577679
|
A | C | 3 | a0005a0014a0018 | 10 | HG00280.hp2 HG02602.hp2 HG02630.hp2 others(7): Show |
missense_variant | MODERATE | c.1393A>C | p.Met465Leu | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 14/32 | 1481/4173 | 1393/3933 | 465/1310 | chr5 | 176577679 | ||
chr5:176577742
|
G | A | 1 | a0019 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.1456G>A | p.Val486Ile | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 14/32 | 1544/4173 | 1456/3933 | 486/1310 | chr5 | 176577742 | ||
chr5:176578417
|
G | A | 2 | a0014a0018 | 3 | HG02630.hp2 HG03195.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.1627G>A | p.Gly543Ser | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/32 | 1715/4173 | 1627/3933 | 543/1310 | chr5 | 176578417 | ||
chr5:176578480
|
G | A | 1 | a0005 | 7 | HG00280.hp2 HG02602.hp2 HG02735.hp2 others(4): Show |
missense_variant | MODERATE | c.1690G>A | p.Gly564Arg | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/32 | 1778/4173 | 1690/3933 | 564/1310 | chr5 | 176578480 | ||
chr5:176581502
|
C | T | 1 | a0015 | 2 | NA19079.hp1 NA19090.hp1 |
missense_variant | MODERATE | c.1978C>T | p.Arg660Cys | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/32 | 2066/4173 | 1978/3933 | 660/1310 | chr5 | 176581502 | ||
chr5:176581538
|
G | A | 1 | a0021 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.2014G>A | p.Glu672Lys | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/32 | 2102/4173 | 2014/3933 | 672/1310 | chr5 | 176581538 | ||
chr5:176584443
|
C | T | 1 | a0020 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.2162C>T | p.Ala721Val | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/32 | 2250/4173 | 2162/3933 | 721/1310 | chr5 | 176584443 | ||
chr5:176584983
|
C | T | 1 | a0010 | 3 | HG00642.hp1 HG01069.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.2702C>T | p.Thr901Met | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/32 | 2790/4173 | 2702/3933 | 901/1310 | chr5 | 176584983 | ||
chr5:176586828
|
G | A | 1 | a0016 | 2 | NA18947.hp2 NA19009.hp1 |
missense_variant | MODERATE | c.2842G>A | p.Val948Met | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/32 | 2930/4173 | 2842/3933 | 948/1310 | chr5 | 176586828 | ||
chr5:176590454
|
C | T | 7 | a0002a0010a0011others(4): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(98): Show |
missense_variant | MODERATE | c.3383C>T | p.Thr1128Met | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 27/32 | 3471/4173 | 3383/3933 | 1128/1310 | chr5 | 176590454 | ||
chr5:176590638
|
C | A | 3 | a0003a0009a0015 | 88 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
missense_variant | MODERATE | c.3490C>A | p.Leu1164Met | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 28/32 | 3578/4173 | 3490/3933 | 1164/1310 | chr5 | 176590638 | ||
chr5:176595583
|
G | A | 2 | a0007a0022 | 6 | HG02055.hp1 HG02717.hp2 HG02922.hp2 others(3): Show |
missense_variant | MODERATE | c.3844G>A | p.Val1282Met | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 32/32 | 3932/4173 | 3844/3933 | 1282/1310 | chr5 | 176595583 | ||
chr5:176595598
|
C | T | 1 | a0013 | 2 | HG02895.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.3859C>T | p.Arg1287Trp | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 32/32 | 3947/4173 | 3859/3933 | 1287/1310 | chr5 | 176595598 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:176571245
|
T | C | 22 | a0001c0005a0001c0008a0001c0016others(19): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
synonymous_variant | LOW | c.348T>C | p.Asp116Asp | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/32 | 436/4173 | 348/3933 | 116/1310 | chr5 | 176571245 | ||
chr5:176575143
|
A | C | 40 | a0001c0003a0001c0005a0001c0006others(37): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
synonymous_variant | LOW | c.555A>C | p.Ile185Ile | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 8/32 | 643/4173 | 555/3933 | 185/1310 | chr5 | 176575143 | ||
chr5:176575541
|
C | T | 9 | a0001c0004a0001c0016a0001c0044others(6): Show | 43 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(40): Show |
synonymous_variant | LOW | c.804C>T | p.Gly268Gly | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 10/32 | 892/4173 | 804/3933 | 268/1310 | chr5 | 176575541 | ||
chr5:176576122
|
C | T | 1 | a0001c0047 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.1131C>T | p.Asp377Asp | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/32 | 1219/4173 | 1131/3933 | 377/1310 | chr5 | 176576122 | ||
chr5:176577509
|
A | G | 2 | a0001c0041a0006c0019 | 3 | HG01884.hp1 HG02572.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.1305A>G | p.Val435Val | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 13/32 | 1393/4173 | 1305/3933 | 435/1310 | chr5 | 176577509 | ||
chr5:176577512
|
C | T | 1 | a0002c0053 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.1308C>T | p.Ser436Ser | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 13/32 | 1396/4173 | 1308/3933 | 436/1310 | chr5 | 176577512 | ||
chr5:176577527
|
C | T | 1 | a0006c0014 | 3 | HG02622.hp1 HG03041.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.1323C>T | p.Tyr441Tyr | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 13/32 | 1411/4173 | 1323/3933 | 441/1310 | chr5 | 176577527 | ||
chr5:176577750
|
G | A | 1 | a0001c0044 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.1464G>A | p.Thr488Thr | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 14/32 | 1552/4173 | 1464/3933 | 488/1310 | chr5 | 176577750 | ||
chr5:176578401
|
G | A | 2 | a0014c0020a0018c0035 | 3 | HG02630.hp2 HG03195.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.1611G>A | p.Thr537Thr | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/32 | 1699/4173 | 1611/3933 | 537/1310 | chr5 | 176578401 | ||
chr5:176578476
|
C | T | 32 | a0001c0003a0001c0004a0001c0006others(29): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
synonymous_variant | LOW | c.1686C>T | p.Asp562Asp | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/32 | 1774/4173 | 1686/3933 | 562/1310 | chr5 | 176578476 | ||
chr5:176581537
|
C | T | 1 | a0003c0037 | 1 | NA18954.hp1 | synonymous_variant | LOW | c.2013C>T | p.Gly671Gly | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/32 | 2101/4173 | 2013/3933 | 671/1310 | chr5 | 176581537 | ||
chr5:176584423
|
C | T | 1 | a0004c0042 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.2142C>T | p.Gly714Gly | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/32 | 2230/4173 | 2142/3933 | 714/1310 | chr5 | 176584423 | ||
chr5:176584441
|
C | T | 1 | a0002c0052 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.2160C>T | p.Asp720Asp | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/32 | 2248/4173 | 2160/3933 | 720/1310 | chr5 | 176584441 | ||
chr5:176584849
|
C | T | 2 | a0007c0027a0022c0054 | 3 | HG02922.hp2 HG03516.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.2568C>T | p.Val856Val | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/32 | 2656/4173 | 2568/3933 | 856/1310 | chr5 | 176584849 | ||
chr5:176584888
|
G | A | 6 | a0001c0003a0001c0008a0001c0013others(3): Show | 52 | HG00323.hp2 HG00642.hp2 HG00735.hp1 others(49): Show |
synonymous_variant | LOW | c.2607G>A | p.Ala869Ala | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/32 | 2695/4173 | 2607/3933 | 869/1310 | chr5 | 176584888 | ||
chr5:176584933
|
C | T | 4 | a0001c0008a0001c0013a0001c0038others(1): Show | 11 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(8): Show |
synonymous_variant | LOW | c.2652C>T | p.Tyr884Tyr | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/32 | 2740/4173 | 2652/3933 | 884/1310 | chr5 | 176584933 | ||
chr5:176589138
|
G | C | 1 | a0001c0017 | 3 | HG02976.hp1 HG03098.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.2964G>C | p.Ser988Ser | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 22/32 | 3052/4173 | 2964/3933 | 988/1310 | chr5 | 176589138 | ||
chr5:176589614
|
T | C | 1 | a0001c0017 | 3 | HG02976.hp1 HG03098.hp1 NA18906.hp1 |
splice_region_variant&synonymous_variant | LOW | c.3204T>C | p.Asn1068Asn | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 24/32 | 3292/4173 | 3204/3933 | 1068/1310 | chr5 | 176589614 | ||
chr5:176590583
|
G | A | 1 | a0001c0046 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.3435G>A | p.Glu1145Glu | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 28/32 | 3523/4173 | 3435/3933 | 1145/1310 | chr5 | 176590583 | ||
chr5:176595663
|
G | A | 1 | a0003c0036 | 1 | HG01981.hp2 | synonymous_variant | LOW | c.3924G>A | p.Thr1308Thr | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 32/32 | 4012/4173 | 3924/3933 | 1308/1310 | chr5 | 176595663 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:176549396
|
C | T | 1 | a0001c0003t0003 | 1 | HG03017.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-34C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/32 | chr5 | 176549396 | ||||||
chr5:176595789
|
C | T | 1 | a0001c0004t0002 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*117C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 32/32 | 117 | chr5 | 176595789 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:176549433
|
A | G | 1 | a0001c0003t0001g0318 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-16+19A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176549433 | ||||||
chr5:176549666
|
A | C | 304 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(301): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.-16+252A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176549666 | ||||||
chr5:176549761
|
C | T | 4 | a0002c0001t0001g0038a0007c0027t0001g0035a0007c0027t0001g0036others(1): Show | 4 | HG02109.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+347C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176549761 | ||||||
chr5:176549796
|
C | T | 4 | a0001c0048t0001g0315a0002c0001t0001g0038a0007c0031t0001g0316others(1): Show | 4 | HG01891.hp2 HG02109.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+382C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176549796 | ||||||
chr5:176549925
|
A | G | 2 | a0008c0011t0001g0313a0012c0021t0001g0314 | 2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-16+511A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176549925 | ||||||
chr5:176549947
|
C | A | 1 | a0001c0003t0001g0039 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-16+533C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176549947 | ||||||
chr5:176549970
|
A | T | 1 | a0004c0009t0001g0312 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-16+556A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176549970 | ||||||
chr5:176549995
|
C | G | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-16+581C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176549995 | ||||||
chr5:176550060
|
T | G | 303 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(300): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.-16+646T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176550060 | ||||||
chr5:176550160
|
G | A | 1 | a0004c0039t0001g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-16+746G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176550160 | ||||||
chr5:176550185
|
G | A | 2 | a0001c0004t0001g0040a0003c0045t0001g0041 | 2 | HG01081.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-16+771G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176550185 | ||||||
chr5:176550189
|
G | A | 2 | a0008c0011t0001g0313a0012c0021t0001g0314 | 2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-16+775G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176550189 | ||||||
chr5:176550525
|
C | T | 8 | a0001c0003t0001g0023a0001c0003t0001g0304a0001c0003t0001g0305others(5): Show | 9 | HG00642.hp2 HG00735.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16+1111C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176550525 | ||||||
chr5:176550755
|
A | C | 1 | a0003c0002t0001g0303 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-16+1341A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176550755 | ||||||
chr5:176550766
|
C | A | 2 | a0008c0011t0001g0313a0012c0021t0001g0314 | 2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-16+1352C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176550766 | ||||||
chr5:176550865
|
C | T | 1 | a0011c0028t0001g0302 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-16+1451C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176550865 | ||||||
chr5:176551123
|
C | T | 46 | a0001c0003t0001g0301a0001c0004t0001g0022a0001c0004t0001g0040others(43): Show | 46 | HG00280.hp1 HG00423.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.-16+1709C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551123 | ||||||
chr5:176551292
|
C | T | 13 | a0001c0003t0001g0021a0001c0003t0001g0023a0001c0003t0001g0256others(10): Show | 15 | HG00642.hp2 HG00735.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16+1878C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551292 | ||||||
chr5:176551317
|
G | A | 1 | a0002c0023t0001g0042 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-16+1903G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551317 | ||||||
chr5:176551369
|
T | C | 2 | a0006c0019t0001g0043a0006c0019t0001g0044 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-16+1955T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551369 | ||||||
chr5:176551389
|
G | A | 6 | a0001c0003t0001g0047a0001c0003t0001g0048a0001c0005t0001g0046others(3): Show | 9 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16+1975G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551389 | ||||||
chr5:176551444
|
A | G | 2 | a0008c0011t0001g0313a0012c0021t0001g0314 | 2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-16+2030A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551444 | ||||||
chr5:176551529
|
C | T | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-16+2115C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551529 | ||||||
chr5:176551530
|
G | A | 4 | a0002c0001t0001g0049a0002c0001t0001g0050a0002c0001t0001g0051others(1): Show | 4 | HG01243.hp1 HG02818.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+2116G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551530 | ||||||
chr5:176551542
|
G | A | 1 | a0004c0039t0001g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-16+2128G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551542 | ||||||
chr5:176551701
|
C | CT | 97 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(94): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.-16+2305dupT | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176551701 | |||||
chr5:176551701
|
C | CTT | 53 | a0001c0003t0001g0047a0001c0003t0001g0048a0001c0003t0001g0160others(50): Show | 59 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.-16+2304_-16+2305d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176551701 | |||||
chr5:176551701
|
C | CTTT | 66 | a0001c0003t0001g0039a0001c0004t0001g0022a0001c0004t0001g0040others(63): Show | 68 | HG00280.hp1 HG00733.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.-16+2303_-16+2305d others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176551701 | |||||
chr5:176551701
|
C | CTTTT | 74 | a0001c0004t0001g0299a0001c0004t0001g0300a0001c0005t0001g0018others(71): Show | 77 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.-16+2302_-16+2305d others(6): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176551701 | |||||
chr5:176551701
|
C | CTTTTT | 9 | a0001c0003t0001g0301a0003c0002t0001g0248a0003c0002t0001g0249others(6): Show | 9 | HG01361.hp1 HG03942.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+2301_-16+2305d others(7): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176551701 | |||||
chr5:176551846
|
C | T | 1 | a0012c0021t0001g0314 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-16+2432C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551846 | ||||||
chr5:176551867
|
AAT | A | 105 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(102): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-16+2456_-16+2457d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176551867 | |||||
chr5:176551870
|
AT | A | 185 | a0001c0003t0001g0039a0001c0003t0001g0047a0001c0003t0001g0048others(182): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-16+2470delT | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176551870 | |||||
chr5:176551872
|
T | A | 2 | a0008c0011t0001g0313a0012c0021t0001g0314 | 2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-16+2458T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551872 | ||||||
chr5:176551882
|
T | G | 80 | a0001c0004t0001g0260a0001c0005t0001g0018a0001c0005t0001g0200others(77): Show | 83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.-16+2468T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551882 | ||||||
chr5:176551883
|
T | G | 141 | a0001c0003t0001g0039a0001c0003t0001g0301a0001c0004t0001g0022others(138): Show | 147 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.-16+2469T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551883 | ||||||
chr5:176551884
|
T | G | 147 | a0001c0003t0001g0039a0001c0003t0001g0301a0001c0004t0001g0022others(144): Show | 153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-16+2470T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551884 | ||||||
chr5:176551885
|
G | T | 108 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(105): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-16+2471G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551885 | ||||||
chr5:176551949
|
C | T | 1 | a0002c0052t0001g0155 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-16+2535C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551949 | ||||||
chr5:176551958
|
A | G | 1 | a0001c0003t0001g0163 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-16+2544A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176551958 | ||||||
chr5:176552006
|
G | A | 2 | a0002c0001t0001g0129a0002c0001t0001g0130 | 2 | HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-16+2592G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176552006 | ||||||
chr5:176552060
|
C | T | 45 | a0001c0003t0001g0039a0001c0003t0001g0301a0001c0004t0001g0022others(42): Show | 45 | HG00280.hp1 HG00423.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.-16+2646C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176552060 | ||||||
chr5:176552098
|
C | T | 2 | a0001c0005t0001g0013a0001c0005t0001g0173 | 3 | HG03139.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-16+2684C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176552098 | ||||||
chr5:176552176
|
C | T | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-16+2762C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176552176 | ||||||
chr5:176552283
|
G | A | 137 | a0001c0003t0001g0039a0001c0003t0001g0301a0001c0004t0001g0022others(134): Show | 143 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-16+2869G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176552283 | ||||||
chr5:176552309
|
T | C | 247 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(244): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.-16+2895T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176552309 | ||||||
chr5:176552328
|
A | G | 110 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(107): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.-16+2914A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176552328 | ||||||
chr5:176552475
|
A | G | 110 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(107): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.-16+3061A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176552475 | ||||||
chr5:176552602
|
G | A | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-16+3188G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176552602 | ||||||
chr5:176552608
|
G | A | 8 | a0001c0004t0001g0169a0001c0005t0001g0013a0001c0005t0001g0173others(5): Show | 9 | HG01884.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16+3194G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176552608 | ||||||
chr5:176552608
|
G | C | 47 | a0001c0003t0001g0047a0001c0003t0001g0048a0001c0004t0001g0179others(44): Show | 52 | HG00099.hp2 HG00735.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.-16+3194G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176552608 | ||||||
chr5:176552609
|
C | T | 47 | a0001c0003t0001g0047a0001c0003t0001g0048a0001c0004t0001g0179others(44): Show | 52 | HG00099.hp2 HG00735.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.-16+3195C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176552609 | ||||||
chr5:176552625
|
CTG | C | 6 | a0001c0004t0001g0169a0001c0006t0001g0170a0001c0008t0001g0165others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+3214_-16+3215d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176552625 | |||||
chr5:176552725
|
C | T | 44 | a0001c0003t0001g0039a0001c0003t0001g0301a0001c0004t0001g0022others(41): Show | 44 | HG00280.hp1 HG00423.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-16+3311C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176552725 | ||||||
chr5:176552816
|
A | G | 293 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(290): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-16+3402A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176552816 | ||||||
chr5:176553053
|
G | C | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-16+3639G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176553053 | ||||||
chr5:176553112
|
T | C | 110 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(107): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.-16+3698T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176553112 | ||||||
chr5:176553152
|
C | T | 7 | a0002c0001t0001g0123a0002c0001t0001g0124a0002c0001t0001g0125others(4): Show | 7 | NA18967.hp1 NA18975.hp1 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+3738C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176553152 | ||||||
chr5:176553238
|
G | A | 2 | a0003c0002t0001g0183a0003c0002t0001g0248 | 2 | NA18612.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.-16+3824G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176553238 | ||||||
chr5:176553241
|
T | C | 46 | a0001c0003t0001g0047a0001c0003t0001g0048a0001c0004t0001g0179others(43): Show | 51 | HG00099.hp2 HG00735.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.-16+3827T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176553241 | ||||||
chr5:176553263
|
C | A | 1 | a0001c0003t0001g0304 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-16+3849C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176553263 | ||||||
chr5:176553297
|
G | A | 2 | a0001c0048t0001g0315a0012c0021t0001g0037 | 2 | HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-16+3883G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176553297 | ||||||
chr5:176553322
|
G | A | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-16+3908G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176553322 | ||||||
chr5:176553463
|
G | A | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+4049G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176553463 | ||||||
chr5:176553606
|
C | T | 2 | a0002c0001t0001g0153a0002c0001t0001g0154 | 2 | HG00099.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-16+4192C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176553606 | ||||||
chr5:176553706
|
C | T | 1 | a0022c0054t0001g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-16+4292C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176553706 | ||||||
chr5:176553880
|
C | A | 78 | a0001c0004t0001g0059a0001c0005t0001g0018a0001c0005t0001g0200others(75): Show | 81 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.-16+4466C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176553880 | ||||||
chr5:176553944
|
T | C | 307 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(304): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-16+4530T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176553944 | ||||||
chr5:176553945
|
G | A | 1 | a0003c0002t0001g0184 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-16+4531G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176553945 | ||||||
chr5:176554042
|
G | A | 6 | a0001c0017t0001g0134a0001c0017t0001g0135a0002c0001t0001g0132others(3): Show | 6 | HG01167.hp2 HG02055.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+4628G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176554042 | ||||||
chr5:176554073
|
T | C | 110 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(107): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.-16+4659T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176554073 | ||||||
chr5:176554108
|
C | T | 2 | a0003c0002t0001g0242a0003c0002t0001g0243 | 2 | NA18969.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-16+4694C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176554108 | ||||||
chr5:176554135
|
C | T | 1 | a0001c0003t0001g0122 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-16+4721C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176554135 | ||||||
chr5:176554417
|
G | C | 1 | a0003c0002t0001g0184 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-16+5003G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176554417 | ||||||
chr5:176554448
|
C | T | 6 | a0001c0004t0001g0169a0001c0006t0001g0170a0001c0008t0001g0165others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+5034C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176554448 | ||||||
chr5:176554477
|
G | T | 6 | a0003c0002t0001g0237a0003c0002t0001g0238a0003c0002t0001g0239others(3): Show | 6 | HG01256.hp1 HG01952.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+5063G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176554477 | ||||||
chr5:176554656
|
T | G | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-16+5242T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176554656 | ||||||
chr5:176554691
|
C | T | 1 | a0012c0021t0001g0314 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-16+5277C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176554691 | ||||||
chr5:176554757
|
T | C | 1 | a0001c0041t0001g0264 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-16+5343T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176554757 | ||||||
chr5:176554842
|
C | T | 123 | a0001c0003t0001g0047a0001c0003t0001g0048a0001c0004t0001g0179others(120): Show | 130 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-16+5428C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176554842 | ||||||
chr5:176555058
|
G | A | 2 | a0001c0016t0001g0014a0001c0016t0001g0137 | 3 | HG02965.hp2 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-16+5644G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555058 | ||||||
chr5:176555192
|
T | G | 128 | a0001c0003t0001g0047a0001c0003t0001g0048a0001c0004t0001g0059others(125): Show | 136 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.-16+5778T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555192 | ||||||
chr5:176555300
|
C | T | 1 | a0003c0002t0001g0244 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-16+5886C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555300 | ||||||
chr5:176555307
|
C | G | 185 | a0001c0003t0001g0047a0001c0003t0001g0048a0001c0003t0001g0301others(182): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-16+5893C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555307 | ||||||
chr5:176555354
|
G | A | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-16+5940G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555354 | ||||||
chr5:176555391
|
A | C | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+5977A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555391 | ||||||
chr5:176555471
|
A | T | 1 | a0003c0002t0001g0236 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-16+6057A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555471 | ||||||
chr5:176555514
|
C | G | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-16+6100C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555514 | ||||||
chr5:176555557
|
G | A | 6 | a0001c0003t0001g0047a0001c0003t0001g0048a0001c0005t0001g0046others(3): Show | 9 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16+6143G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555557 | ||||||
chr5:176555579
|
G | A | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-16+6165G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555579 | ||||||
chr5:176555620
|
G | A | 5 | a0001c0006t0001g0141a0002c0001t0001g0140a0002c0001t0001g0142others(2): Show | 5 | HG02922.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+6206G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555620 | ||||||
chr5:176555644
|
C | T | 1 | a0001c0047t0001g0174 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-16+6230C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555644 | ||||||
chr5:176555672
|
C | T | 1 | a0002c0001t0001g0235 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-16+6258C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555672 | ||||||
chr5:176555704
|
C | T | 3 | a0001c0003t0001g0012a0003c0032t0001g0120a0003c0032t0001g0121 | 4 | HG01070.hp1 HG01071.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+6290C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555704 | ||||||
chr5:176555752
|
A | C | 299 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(296): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-16+6338A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555752 | ||||||
chr5:176555788
|
TC | T | 168 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(165): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.-16+6376delC | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176555788 | |||||
chr5:176555815
|
C | A | 1 | a0002c0001t0001g0060 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-16+6401C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555815 | ||||||
chr5:176555888
|
A | G | 301 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(298): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-16+6474A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555888 | ||||||
chr5:176555909
|
CA | C | 289 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(286): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-16+6503delA | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176555909 | |||||
chr5:176555917
|
A | C | 1 | a0001c0003t0001g0061 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-16+6503A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176555917 | ||||||
chr5:176555917
|
AC | A | 10 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(7): Show | 10 | HG02451.hp2 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-16+6508delC | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176555917 | |||||
chr5:176556149
|
C | T | 2 | a0001c0005t0001g0013a0001c0005t0001g0173 | 3 | HG03139.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-16+6735C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556149 | ||||||
chr5:176556192
|
T | C | 2 | a0001c0005t0001g0013a0001c0005t0001g0173 | 3 | HG03139.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-16+6778T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556192 | ||||||
chr5:176556242
|
A | ACCTGTAA others(156): Show |
1 | a0001c0006t0001g0233 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-16+6891_-16+6892i others(165): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176556242 | |||||
chr5:176556306
|
C | T | 78 | a0001c0005t0001g0018a0001c0005t0001g0200a0001c0025t0001g0195others(75): Show | 81 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.-16+6892C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556306 | ||||||
chr5:176556325
|
C | T | 1 | a0002c0001t0001g0119 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-16+6911C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556325 | ||||||
chr5:176556330
|
T | C | 2 | a0001c0005t0001g0013a0001c0005t0001g0173 | 3 | HG03139.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-16+6916T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556330 | ||||||
chr5:176556355
|
C | T | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-16+6941C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556355 | ||||||
chr5:176556388
|
C | T | 1 | a0002c0001t0001g0128 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-16+6974C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556388 | ||||||
chr5:176556393
|
G | A | 129 | a0001c0003t0001g0047a0001c0003t0001g0048a0001c0004t0001g0179others(126): Show | 139 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-16+6979G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556393 | ||||||
chr5:176556395
|
G | A | 1 | a0002c0001t0001g0128 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-16+6981G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556395 | ||||||
chr5:176556457
|
G | C | 1 | a0001c0004t0001g0265 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-16+7043G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556457 | ||||||
chr5:176556473
|
C | T | 2 | a0001c0004t0001g0295a0001c0005t0001g0296 | 2 | HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-16+7059C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556473 | ||||||
chr5:176556474
|
G | A | 2 | a0002c0001t0001g0153a0002c0001t0001g0154 | 2 | HG00099.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-16+7060G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556474 | ||||||
chr5:176556482
|
T | C | 1 | a0001c0004t0001g0266 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-16+7068T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556482 | ||||||
chr5:176556493
|
A | C | 1 | a0001c0004t0001g0266 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-16+7079A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556493 | ||||||
chr5:176556494
|
G | A | 1 | a0001c0004t0001g0266 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-16+7080G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556494 | ||||||
chr5:176556534
|
A | G | 1 | a0001c0004t0001g0294 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-16+7120A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556534 | ||||||
chr5:176556589
|
C | A | 1 | a0003c0002t0001g0185 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-16+7175C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556589 | ||||||
chr5:176556590
|
G | A | 1 | a0003c0002t0001g0183 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-16+7176G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556590 | ||||||
chr5:176556597
|
G | A | 1 | a0004c0042t0001g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-16+7183G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556597 | ||||||
chr5:176556614
|
G | A | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-16+7200G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556614 | ||||||
chr5:176556784
|
T | G | 2 | a0006c0019t0001g0043a0006c0019t0001g0044 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-16+7370T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176556784 | ||||||
chr5:176557000
|
TTC | T | 12 | a0001c0016t0001g0014a0001c0016t0001g0137a0002c0052t0001g0155others(9): Show | 14 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-16+7602_-16+7603d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557000 | |||||
chr5:176557000
|
TTCTC | T | 55 | a0001c0003t0001g0301a0001c0004t0001g0022a0001c0004t0001g0040others(52): Show | 58 | HG00280.hp1 HG00423.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.-16+7600_-16+7603d others(6): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557000 | |||||
chr5:176557013
|
TC | T | 19 | a0001c0006t0001g0141a0001c0038t0001g0152a0002c0001t0001g0015others(16): Show | 20 | HG00099.hp2 HG00735.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+7600delC | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557013 | ||||||
chr5:176557013
|
TCTC | T | 89 | a0001c0005t0001g0018a0001c0005t0001g0200a0001c0006t0001g0233others(86): Show | 92 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-16+7600_-16+7602d others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557013 | ||||||
chr5:176557014
|
C | T | 7 | a0001c0017t0001g0134a0001c0017t0001g0135a0002c0001t0001g0052others(4): Show | 7 | HG01167.hp2 HG02055.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16+7600C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557014 | ||||||
chr5:176557014
|
CTCTT | C | 119 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(116): Show | 135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-16+7602_-16+7605d others(6): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557014 | |||||
chr5:176557016
|
C | T | 38 | a0001c0006t0001g0141a0001c0016t0001g0014a0001c0016t0001g0137others(35): Show | 41 | HG00099.hp2 HG00735.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.-16+7602C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557016 | ||||||
chr5:176557148
|
T | TAGGACCA others(1): Show |
304 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(301): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.-16+7738_-16+7745d others(10): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557148 | |||||
chr5:176557172
|
C | T | 1 | a0002c0001t0001g0118 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-16+7758C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557172 | ||||||
chr5:176557197
|
TTTG | T | 293 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(290): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-16+7789_-16+7791d others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557197 | |||||
chr5:176557216
|
T | G | 133 | a0001c0004t0001g0059a0001c0005t0001g0013a0001c0005t0001g0018others(130): Show | 142 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.-16+7802T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557216 | ||||||
chr5:176557277
|
C | T | 42 | a0001c0003t0001g0301a0001c0004t0001g0022a0001c0004t0001g0040others(39): Show | 42 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.-16+7863C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557277 | ||||||
chr5:176557280
|
C | A | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+7866C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557280 | ||||||
chr5:176557490
|
G | A | 2 | a0006c0019t0001g0043a0006c0019t0001g0044 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-15-7848G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557490 | ||||||
chr5:176557502
|
G | A | 1 | a0003c0002t0001g0188 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-15-7836G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557502 | ||||||
chr5:176557538
|
C | T | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-7800C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557538 | ||||||
chr5:176557560
|
A | AT | 102 | a0001c0003t0001g0012a0001c0003t0001g0318a0001c0005t0001g0018others(99): Show | 110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-15-7755dupT | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557560 | |||||
chr5:176557560
|
A | ATT | 16 | a0001c0005t0001g0013a0001c0005t0001g0173a0001c0006t0001g0117others(13): Show | 17 | HG01928.hp1 HG01993.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.-15-7756_-15-7755d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557560 | |||||
chr5:176557560
|
AT | A | 45 | a0001c0003t0001g0023a0001c0003t0001g0301a0001c0003t0001g0305others(42): Show | 46 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-15-7755delT | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557560 | |||||
chr5:176557560
|
ATT | A | 8 | a0001c0004t0001g0169a0001c0004t0001g0270a0001c0006t0001g0170others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-7756_-15-7755d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557560 | |||||
chr5:176557568
|
T | C | 1 | a0001c0004t0001g0268 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-15-7770T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557568 | ||||||
chr5:176557593
|
T | G | 1 | a0002c0053t0001g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-15-7745T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557593 | ||||||
chr5:176557605
|
G | A | 48 | a0001c0003t0001g0301a0001c0004t0001g0022a0001c0004t0001g0040others(45): Show | 48 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.-15-7733G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557605 | ||||||
chr5:176557608
|
C | G | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-7730C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557608 | ||||||
chr5:176557682
|
T | TTCTCTTC others(53): Show |
2 | a0001c0008t0001g0176a0001c0008t0001g0177 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-15-7655_-15-7654i others(62): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557682 | |||||
chr5:176557682
|
T | TTCTCTTC others(73): Show |
2 | a0014c0020t0001g0180a0014c0020t0001g0181 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-15-7655_-15-7654i others(82): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557682 | |||||
chr5:176557682
|
T | TTCTCTTC others(69): Show |
1 | a0018c0035t0001g0182 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-15-7655_-15-7654i others(78): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557682 | |||||
chr5:176557682
|
T | TTCTCTTC others(53): Show |
1 | a0001c0008t0001g0178 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-15-7655_-15-7654i others(62): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557682 | |||||
chr5:176557686
|
T | C | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-7652T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557686 | ||||||
chr5:176557686
|
TTTTC | T | 127 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0173others(124): Show | 136 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.-15-7628_-15-7625d others(6): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557686 | |||||
chr5:176557686
|
TTTTCTTT others(1): Show |
T | 112 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(109): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-15-7632_-15-7625d others(10): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557686 | |||||
chr5:176557694
|
C | T | 34 | a0001c0006t0001g0141a0001c0017t0001g0134a0001c0017t0001g0135others(31): Show | 37 | HG00099.hp2 HG00735.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.-15-7644C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557694 | ||||||
chr5:176557697
|
T | G | 7 | a0001c0004t0001g0268a0001c0004t0001g0271a0001c0004t0001g0272others(4): Show | 7 | HG01975.hp1 NA18939.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15-7641T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557697 | ||||||
chr5:176557705
|
T | C | 3 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-15-7633T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557705 | ||||||
chr5:176557706
|
C | T | 3 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-15-7632C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557706 | ||||||
chr5:176557711
|
T | TTCTTTTC others(4): Show |
3 | a0014c0020t0001g0180a0014c0020t0001g0181a0018c0035t0001g0182 | 3 | HG02630.hp2 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-15-7626_-15-7625i others(13): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176557711 | |||||
chr5:176557715
|
T | C | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-7623T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557715 | ||||||
chr5:176557719
|
T | C | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-7619T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557719 | ||||||
chr5:176557897
|
A | G | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-7441A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557897 | ||||||
chr5:176557979
|
T | A | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-7359T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557979 | ||||||
chr5:176557995
|
C | T | 1 | a0002c0001t0001g0109 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-15-7343C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176557995 | ||||||
chr5:176558063
|
G | A | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-7275G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558063 | ||||||
chr5:176558124
|
C | T | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-7214C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558124 | ||||||
chr5:176558159
|
A | G | 132 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0173others(129): Show | 141 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.-15-7179A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558159 | ||||||
chr5:176558195
|
T | G | 3 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-15-7143T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558195 | ||||||
chr5:176558212
|
T | C | 171 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(168): Show | 187 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.-15-7126T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558212 | ||||||
chr5:176558214
|
AT | A | 182 | a0001c0003t0001g0107a0001c0003t0001g0301a0001c0004t0001g0022others(179): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.-15-7105delT | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176558214 | |||||
chr5:176558214
|
ATT | A | 117 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(114): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.-15-7106_-15-7105d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176558214 | |||||
chr5:176558218
|
T | A | 2 | a0001c0005t0001g0173a0004c0009t0001g0147 | 2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-15-7120T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558218 | ||||||
chr5:176558219
|
T | A | 126 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0200others(123): Show | 133 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-15-7119T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558219 | ||||||
chr5:176558220
|
T | A | 2 | a0002c0001t0001g0133a0009c0015t0001g0193 | 2 | HG01975.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-15-7118T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558220 | ||||||
chr5:176558223
|
T | A | 1 | a0012c0021t0001g0314 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-15-7115T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558223 | ||||||
chr5:176558238
|
C | T | 3 | a0014c0020t0001g0180a0014c0020t0001g0181a0018c0035t0001g0182 | 3 | HG02630.hp2 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-15-7100C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558238 | ||||||
chr5:176558246
|
C | T | 1 | a0016c0029t0001g0275 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-15-7092C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558246 | ||||||
chr5:176558255
|
G | A | 6 | a0002c0001t0001g0015a0002c0001t0001g0148a0002c0001t0001g0149others(3): Show | 7 | HG00099.hp2 HG00735.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-7083G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558255 | ||||||
chr5:176558302
|
G | A | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-7036G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558302 | ||||||
chr5:176558368
|
A | G | 4 | a0004c0009t0001g0146a0004c0009t0001g0147a0004c0009t0001g0312others(1): Show | 4 | HG01891.hp1 HG02559.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-6970A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558368 | ||||||
chr5:176558377
|
A | G | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-6961A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558377 | ||||||
chr5:176558382
|
AT | A | 46 | a0001c0003t0001g0301a0001c0004t0001g0022a0001c0004t0001g0040others(43): Show | 46 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.-15-6938delT | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176558382 | |||||
chr5:176558540
|
C | G | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-6798C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558540 | ||||||
chr5:176558540
|
C | T | 297 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(294): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-15-6798C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558540 | ||||||
chr5:176558571
|
G | A | 5 | a0001c0006t0001g0011a0001c0006t0001g0110a0001c0006t0001g0111others(2): Show | 6 | HG01928.hp1 NA18943.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-6767G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558571 | ||||||
chr5:176558622
|
C | T | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-6716C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558622 | ||||||
chr5:176558665
|
G | A | 2 | a0001c0005t0001g0013a0001c0005t0001g0173 | 3 | HG03139.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-15-6673G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558665 | ||||||
chr5:176558675
|
G | A | 2 | a0013c0022t0001g0261a0013c0022t0001g0262 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-15-6663G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558675 | ||||||
chr5:176558741
|
C | G | 4 | a0006c0019t0001g0043a0006c0019t0001g0044a0013c0022t0001g0261others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-6597C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558741 | ||||||
chr5:176558762
|
C | T | 1 | a0003c0036t0001g0223 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-15-6576C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558762 | ||||||
chr5:176558795
|
C | T | 1 | a0003c0002t0001g0106 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-15-6543C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558795 | ||||||
chr5:176558981
|
A | G | 307 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(304): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-15-6357A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176558981 | ||||||
chr5:176559036
|
G | A | 1 | a0001c0025t0001g0195 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-15-6302G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176559036 | ||||||
chr5:176559052
|
G | A | 2 | a0002c0001t0001g0113a0002c0001t0001g0114 | 2 | NA18940.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-15-6286G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176559052 | ||||||
chr5:176559082
|
C | T | 42 | a0001c0003t0001g0301a0001c0004t0001g0022a0001c0004t0001g0040others(39): Show | 42 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.-15-6256C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176559082 | ||||||
chr5:176559150
|
C | T | 33 | a0001c0006t0001g0141a0001c0017t0001g0134a0001c0017t0001g0135others(30): Show | 34 | HG00099.hp2 HG00735.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.-15-6188C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176559150 | ||||||
chr5:176559193
|
C | T | 4 | a0006c0019t0001g0043a0006c0019t0001g0044a0013c0022t0001g0261others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-6145C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176559193 | ||||||
chr5:176559292
|
C | T | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-6046C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176559292 | ||||||
chr5:176559713
|
AT | A | 155 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(152): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.-15-5617delT | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176559713 | |||||
chr5:176559721
|
TA | T | 142 | a0001c0004t0001g0169a0001c0005t0001g0013a0001c0005t0001g0018others(139): Show | 151 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-15-5613delA | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176559721 | |||||
chr5:176559722
|
A | T | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-5616A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176559722 | ||||||
chr5:176560078
|
G | A | 2 | a0001c0004t0001g0289a0001c0004t0002g0276 | 2 | HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-15-5260G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560078 | ||||||
chr5:176560168
|
G | A | 42 | a0001c0003t0001g0301a0001c0004t0001g0022a0001c0004t0001g0040others(39): Show | 42 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.-15-5170G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560168 | ||||||
chr5:176560225
|
C | T | 2 | a0001c0005t0001g0013a0001c0005t0001g0173 | 3 | HG03139.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-15-5113C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560225 | ||||||
chr5:176560265
|
C | T | 128 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0173others(125): Show | 137 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.-15-5073C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560265 | ||||||
chr5:176560323
|
G | T | 6 | a0002c0001t0001g0123a0002c0001t0001g0124a0002c0001t0001g0125others(3): Show | 6 | NA18967.hp1 NA18975.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-5015G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560323 | ||||||
chr5:176560331
|
G | T | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-5007G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560331 | ||||||
chr5:176560340
|
G | A | 82 | a0001c0005t0001g0018a0001c0005t0001g0200a0001c0006t0001g0233others(79): Show | 85 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-15-4998G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560340 | ||||||
chr5:176560350
|
C | T | 3 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-15-4988C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560350 | ||||||
chr5:176560375
|
G | A | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-4963G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560375 | ||||||
chr5:176560421
|
A | G | 1 | a0004c0009t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-15-4917A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560421 | ||||||
chr5:176560425
|
G | A | 117 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(114): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.-15-4913G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560425 | ||||||
chr5:176560469
|
A | G | 1 | a0001c0004t0001g0273 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-15-4869A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560469 | ||||||
chr5:176560624
|
G | A | 2 | a0002c0001t0001g0069a0002c0001t0001g0108 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-15-4714G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560624 | ||||||
chr5:176560632
|
C | G | 1 | a0001c0003t0001g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-15-4706C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560632 | ||||||
chr5:176560758
|
C | A | 1 | a0003c0002t0001g0185 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-15-4580C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560758 | ||||||
chr5:176560772
|
C | T | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02109.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-4566C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560772 | ||||||
chr5:176560808
|
A | G | 44 | a0001c0006t0001g0141a0001c0016t0001g0014a0001c0016t0001g0137others(41): Show | 49 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.-15-4530A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560808 | ||||||
chr5:176560925
|
G | C | 244 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(241): Show | 264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.-15-4413G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560925 | ||||||
chr5:176560955
|
A | T | 1 | a0003c0002t0001g0222 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-15-4383A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560955 | ||||||
chr5:176560963
|
C | A | 1 | a0001c0025t0001g0195 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-15-4375C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560963 | ||||||
chr5:176560990
|
TG | T | 260 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(257): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.-15-4343delG | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176560990 | |||||
chr5:176560991
|
G | T | 2 | a0003c0002t0001g0242a0003c0002t0001g0243 | 2 | NA18969.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-15-4347G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560991 | ||||||
chr5:176560992
|
G | C | 38 | a0001c0006t0001g0141a0001c0016t0001g0014a0001c0016t0001g0137others(35): Show | 41 | HG00099.hp2 HG00735.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.-15-4346G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176560992 | ||||||
chr5:176561028
|
G | A | 38 | a0001c0006t0001g0141a0001c0016t0001g0014a0001c0016t0001g0137others(35): Show | 41 | HG00099.hp2 HG00735.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.-15-4310G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561028 | ||||||
chr5:176561081
|
G | A | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-4257G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561081 | ||||||
chr5:176561097
|
G | A | 44 | a0001c0006t0001g0141a0001c0016t0001g0014a0001c0016t0001g0137others(41): Show | 49 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.-15-4241G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561097 | ||||||
chr5:176561171
|
C | T | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-4167C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561171 | ||||||
chr5:176561207
|
T | A | 6 | a0004c0010t0001g0016a0004c0010t0001g0017a0008c0011t0001g0171others(3): Show | 8 | HG00733.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-4131T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561207 | ||||||
chr5:176561257
|
G | C | 297 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(294): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-15-4081G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561257 | ||||||
chr5:176561262
|
T | C | 297 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(294): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-15-4076T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561262 | ||||||
chr5:176561294
|
A | G | 297 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(294): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-15-4044A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561294 | ||||||
chr5:176561598
|
A | G | 188 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(185): Show | 199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.-15-3740A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561598 | ||||||
chr5:176561641
|
C | CT | 293 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(290): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-15-3681dupT | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176561641 | |||||
chr5:176561688
|
G | A | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-15-3650G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561688 | ||||||
chr5:176561709
|
G | A | 6 | a0001c0004t0001g0169a0001c0006t0001g0170a0001c0008t0001g0165others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-3629G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561709 | ||||||
chr5:176561710
|
A | G | 103 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(100): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-15-3628A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561710 | ||||||
chr5:176561727
|
C | T | 1 | a0001c0003t0001g0047 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-15-3611C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561727 | ||||||
chr5:176561796
|
C | T | 103 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(100): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-15-3542C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561796 | ||||||
chr5:176561832
|
G | C | 1 | a0001c0004t0001g0271 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-15-3506G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561832 | ||||||
chr5:176561868
|
G | A | 1 | a0001c0003t0001g0160 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-15-3470G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561868 | ||||||
chr5:176561939
|
C | T | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-15-3399C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561939 | ||||||
chr5:176561980
|
G | A | 1 | a0001c0004t0001g0272 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-15-3358G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176561980 | ||||||
chr5:176562027
|
A | G | 103 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(100): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-15-3311A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562027 | ||||||
chr5:176562045
|
G | A | 2 | a0004c0010t0001g0032a0004c0055t0001g0033 | 2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-15-3293G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562045 | ||||||
chr5:176562115
|
G | A | 108 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(105): Show | 115 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-15-3223G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562115 | ||||||
chr5:176562192
|
G | A | 1 | a0001c0003t0001g0318 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-15-3146G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562192 | ||||||
chr5:176562249
|
A | G | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-15-3089A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562249 | ||||||
chr5:176562250
|
G | T | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-15-3088G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562250 | ||||||
chr5:176562339
|
A | G | 1 | a0001c0004t0001g0260 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-15-2999A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562339 | ||||||
chr5:176562352
|
A | AG | 117 | a0001c0003t0001g0107a0001c0004t0001g0059a0001c0006t0001g0011others(114): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.-15-2984dupG | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr5 | 176562352 | |||||
chr5:176562361
|
G | C | 4 | a0006c0019t0001g0043a0006c0019t0001g0044a0013c0022t0001g0261others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-2977G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562361 | ||||||
chr5:176562449
|
G | C | 2 | a0002c0001t0001g0074a0002c0001t0001g0118 | 2 | HG03834.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-15-2889G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562449 | ||||||
chr5:176562455
|
A | G | 103 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(100): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-15-2883A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562455 | ||||||
chr5:176562548
|
G | C | 103 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(100): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-15-2790G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562548 | ||||||
chr5:176562886
|
G | A | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-2452G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562886 | ||||||
chr5:176562954
|
G | A | 8 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(5): Show | 9 | HG02622.hp1 HG02630.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15-2384G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562954 | ||||||
chr5:176562985
|
G | C | 6 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-2353G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562985 | ||||||
chr5:176562990
|
G | A | 305 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(302): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.-15-2348G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176562990 | ||||||
chr5:176563000
|
T | C | 221 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(218): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.-15-2338T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563000 | ||||||
chr5:176563046
|
C | T | 2 | a0002c0001t0001g0069a0002c0001t0001g0108 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-15-2292C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563046 | ||||||
chr5:176563179
|
C | G | 95 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(92): Show | 102 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.-15-2159C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563179 | ||||||
chr5:176563242
|
G | A | 2 | a0003c0002t0001g0164a0003c0002t0001g0196 | 2 | NA20300.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-15-2096G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563242 | ||||||
chr5:176563284
|
G | T | 1 | a0001c0004t0001g0271 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-15-2054G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563284 | ||||||
chr5:176563320
|
C | T | 1 | a0005c0007t0001g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15-2018C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563320 | ||||||
chr5:176563373
|
C | T | 2 | a0001c0003t0001g0306a0002c0001t0001g0096 | 2 | HG00642.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.-15-1965C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563373 | ||||||
chr5:176563405
|
G | T | 1 | a0001c0038t0001g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-15-1933G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563405 | ||||||
chr5:176563439
|
T | A | 1 | a0002c0001t0001g0127 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-15-1899T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563439 | ||||||
chr5:176563440
|
T | C | 1 | a0002c0001t0001g0127 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-15-1898T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563440 | ||||||
chr5:176563443
|
A | G | 1 | a0002c0001t0001g0127 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-15-1895A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563443 | ||||||
chr5:176563444
|
T | A | 1 | a0002c0001t0001g0127 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-15-1894T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563444 | ||||||
chr5:176563446
|
T | C | 1 | a0002c0001t0001g0127 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-15-1892T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563446 | ||||||
chr5:176563449
|
C | T | 1 | a0002c0001t0001g0127 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-15-1889C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563449 | ||||||
chr5:176563469
|
T | C | 1 | a0002c0001t0001g0157 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-15-1869T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563469 | ||||||
chr5:176563516
|
G | T | 4 | a0008c0011t0001g0171a0008c0011t0001g0172a0008c0011t0001g0313others(1): Show | 4 | HG00733.hp2 HG02451.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-1822G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563516 | ||||||
chr5:176563568
|
C | T | 117 | a0001c0003t0001g0107a0001c0004t0001g0059a0001c0006t0001g0011others(114): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.-15-1770C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563568 | ||||||
chr5:176563577
|
T | C | 4 | a0002c0001t0001g0015a0002c0001t0001g0148a0002c0001t0001g0149others(1): Show | 5 | HG00735.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-1761T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563577 | ||||||
chr5:176563632
|
A | T | 309 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(306): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-15-1706A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563632 | ||||||
chr5:176563691
|
A | G | 1 | a0002c0001t0001g0133 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-15-1647A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176563691 | ||||||
chr5:176564240
|
C | A | 10 | a0001c0004t0001g0169a0001c0006t0001g0170a0001c0008t0001g0165others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-15-1098C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564240 | ||||||
chr5:176564278
|
C | T | 1 | a0001c0003t0001g0309 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-15-1060C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564278 | ||||||
chr5:176564279
|
G | A | 5 | a0002c0001t0001g0123a0002c0001t0001g0124a0002c0001t0001g0125others(2): Show | 5 | NA18967.hp1 NA18975.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-1059G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564279 | ||||||
chr5:176564304
|
G | A | 2 | a0001c0005t0001g0013a0001c0005t0001g0173 | 3 | HG03139.hp2 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-15-1034G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564304 | ||||||
chr5:176564321
|
G | A | 3 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-15-1017G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564321 | ||||||
chr5:176564347
|
G | A | 3 | a0001c0008t0001g0176a0001c0008t0001g0177a0001c0008t0001g0178 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-15-991G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564347 | ||||||
chr5:176564396
|
C | T | 10 | a0001c0004t0001g0169a0001c0006t0001g0170a0001c0008t0001g0165others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-15-942C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564396 | ||||||
chr5:176564430
|
C | T | 39 | a0001c0003t0001g0301a0001c0004t0001g0022a0001c0004t0001g0040others(36): Show | 39 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.-15-908C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564430 | ||||||
chr5:176564431
|
G | A | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-15-907G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564431 | ||||||
chr5:176564435
|
G | A | 1 | a0002c0001t0001g0075 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-15-903G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564435 | ||||||
chr5:176564479
|
C | T | 109 | a0001c0003t0001g0107a0001c0005t0001g0311a0001c0006t0001g0011others(106): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.-15-859C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564479 | ||||||
chr5:176564508
|
G | C | 87 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(84): Show | 95 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-15-830G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564508 | ||||||
chr5:176564568
|
C | T | 1 | a0006c0019t0001g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-15-770C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564568 | ||||||
chr5:176564580
|
C | T | 1 | a0002c0001t0001g0050 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-15-758C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564580 | ||||||
chr5:176564645
|
T | C | 1 | a0002c0001t0001g0149 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-15-693T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564645 | ||||||
chr5:176564892
|
T | C | 1 | a0002c0023t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-15-446T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564892 | ||||||
chr5:176564913
|
G | T | 1 | a0004c0039t0001g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-15-425G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564913 | ||||||
chr5:176564948
|
G | A | 1 | a0002c0001t0001g0076 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-15-390G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564948 | ||||||
chr5:176564997
|
G | T | 41 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(38): Show | 48 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.-15-341G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176564997 | ||||||
chr5:176565049
|
G | A | 5 | a0008c0011t0001g0171a0008c0011t0001g0172a0008c0011t0001g0277others(2): Show | 5 | HG00733.hp2 HG02451.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-289G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176565049 | ||||||
chr5:176565066
|
G | A | 41 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(38): Show | 48 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.-15-272G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176565066 | ||||||
chr5:176565073
|
A | G | 266 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(263): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.-15-265A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176565073 | ||||||
chr5:176565108
|
G | C | 1 | a0006c0019t0001g0043 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-15-230G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176565108 | ||||||
chr5:176565219
|
T | C | 1 | a0004c0010t0001g0032 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-15-119T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176565219 | ||||||
chr5:176565257
|
A | G | 265 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(262): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-15-81A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176565257 | ||||||
chr5:176565265
|
C | G | 95 | a0001c0003t0001g0107a0001c0006t0001g0011a0001c0006t0001g0110others(92): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15-73C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 1/31 | chr5 | 176565265 | ||||||
chr5:176565518
|
T | A | 45 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(42): Show | 53 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.52+114T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 2/31 | chr5 | 176565518 | ||||||
chr5:176565635
|
G | T | 4 | a0001c0003t0001g0301a0001c0004t0001g0265a0001c0004t0001g0287others(1): Show | 4 | HG01361.hp1 HG03688.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-37G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 2/31 | chr5 | 176565635 | ||||||
chr5:176565773
|
G | A | 1 | a0002c0023t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.124+30G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176565773 | ||||||
chr5:176565948
|
A | C | 10 | a0001c0004t0001g0169a0004c0009t0001g0146a0004c0009t0001g0147others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+205A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176565948 | ||||||
chr5:176565987
|
C | T | 1 | a0003c0002t0001g0234 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.124+244C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176565987 | ||||||
chr5:176565988
|
G | A | 1 | a0017c0040t0001g0167 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.124+245G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176565988 | ||||||
chr5:176566095
|
C | CT | 9 | a0006c0014t0001g0003a0006c0014t0001g0045a0006c0019t0001g0043others(6): Show | 10 | HG00733.hp2 HG01884.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.124+365dupT | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 176566095 | |||||
chr5:176566105
|
T | C | 1 | a0001c0003t0001g0107 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.124+362T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176566105 | ||||||
chr5:176566195
|
G | A | 9 | a0006c0014t0001g0003a0006c0014t0001g0045a0006c0019t0001g0043others(6): Show | 10 | HG00733.hp2 HG01884.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.124+452G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176566195 | ||||||
chr5:176566199
|
A | G | 93 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(90): Show | 97 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.124+456A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176566199 | ||||||
chr5:176566539
|
AGGAGCCC others(4): Show |
A | 2 | a0001c0004t0001g0286a0001c0004t0001g0300 | 2 | NA18979.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.124+802_124+812del others(11): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 176566539 | |||||
chr5:176566551
|
G | A | 5 | a0003c0002t0001g0237a0003c0002t0001g0238a0003c0002t0001g0239others(2): Show | 5 | HG01256.hp1 HG01952.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+808G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176566551 | ||||||
chr5:176566606
|
G | A | 2 | a0006c0014t0001g0003a0006c0014t0001g0045 | 3 | HG02622.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.124+863G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176566606 | ||||||
chr5:176566619
|
C | G | 1 | a0001c0041t0001g0264 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.124+876C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176566619 | ||||||
chr5:176566679
|
G | A | 1 | a0003c0002t0001g0249 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.124+936G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176566679 | ||||||
chr5:176566785
|
C | A | 1 | a0014c0020t0001g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.124+1042C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176566785 | ||||||
chr5:176566797
|
C | T | 8 | a0006c0014t0001g0003a0006c0014t0001g0045a0006c0019t0001g0043others(5): Show | 9 | HG00733.hp2 HG01884.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.124+1054C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176566797 | ||||||
chr5:176566807
|
C | T | 1 | a0003c0002t0001g0183 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.124+1064C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176566807 | ||||||
chr5:176566818
|
A | G | 46 | a0001c0003t0001g0301a0001c0004t0001g0022a0001c0004t0001g0040others(43): Show | 46 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.124+1075A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176566818 | ||||||
chr5:176567020
|
A | G | 2 | a0006c0014t0001g0003a0006c0014t0001g0045 | 3 | HG02622.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.124+1277A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176567020 | ||||||
chr5:176567124
|
A | G | 41 | a0001c0003t0001g0301a0001c0004t0001g0022a0001c0004t0001g0040others(38): Show | 41 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.124+1381A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176567124 | ||||||
chr5:176567172
|
C | CT | 204 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(201): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.124+1443dupT | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 176567172 | |||||
chr5:176567172
|
C | CTT | 86 | a0001c0003t0001g0107a0001c0005t0001g0018a0001c0005t0001g0200others(83): Show | 89 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.124+1442_124+1443d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr5 | 176567172 | |||||
chr5:176567261
|
G | T | 8 | a0006c0014t0001g0003a0006c0014t0001g0045a0006c0019t0001g0043others(5): Show | 9 | HG00733.hp2 HG01884.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-1417G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176567261 | ||||||
chr5:176567412
|
C | T | 3 | a0001c0006t0001g0141a0002c0001t0001g0140a0002c0001t0001g0142 | 3 | HG02976.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.125-1266C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176567412 | ||||||
chr5:176567682
|
G | A | 1 | a0003c0002t0001g0246 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.125-996G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176567682 | ||||||
chr5:176567719
|
C | T | 1 | a0001c0003t0003g0105 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.125-959C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176567719 | ||||||
chr5:176567726
|
C | T | 2 | a0007c0027t0001g0035a0007c0027t0001g0036 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.125-952C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176567726 | ||||||
chr5:176567777
|
G | A | 139 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(136): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.125-901G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176567777 | ||||||
chr5:176567832
|
T | C | 4 | a0001c0004t0001g0278a0001c0004t0001g0279a0001c0004t0001g0289others(1): Show | 4 | HG00280.hp1 HG01255.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-846T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176567832 | ||||||
chr5:176567888
|
C | T | 139 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(136): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.125-790C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176567888 | ||||||
chr5:176567895
|
C | T | 139 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(136): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.125-783C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176567895 | ||||||
chr5:176567951
|
A | G | 1 | a0022c0054t0001g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.125-727A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176567951 | ||||||
chr5:176567968
|
G | A | 139 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(136): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.125-710G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176567968 | ||||||
chr5:176568099
|
T | A | 1 | a0008c0011t0001g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.125-579T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176568099 | ||||||
chr5:176568391
|
G | T | 141 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(138): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.125-287G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176568391 | ||||||
chr5:176568449
|
C | T | 1 | a0022c0054t0001g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.125-229C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176568449 | ||||||
chr5:176568465
|
G | A | 1 | a0017c0040t0001g0167 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.125-213G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176568465 | ||||||
chr5:176568570
|
C | G | 192 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(189): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.125-108C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 3/31 | chr5 | 176568570 | ||||||
chr5:176568834
|
G | A | 90 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(87): Show | 94 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.264+17G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 4/31 | chr5 | 176568834 | ||||||
chr5:176568856
|
G | C | 41 | a0001c0003t0001g0301a0001c0004t0001g0022a0001c0004t0001g0040others(38): Show | 41 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.264+39G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 4/31 | chr5 | 176568856 | ||||||
chr5:176568912
|
C | A | 86 | a0001c0005t0001g0018a0001c0005t0001g0200a0001c0025t0001g0195others(83): Show | 89 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.265-48C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 4/31 | chr5 | 176568912 | ||||||
chr5:176568934
|
C | T | 147 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(144): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.265-26C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 4/31 | chr5 | 176568934 | ||||||
chr5:176568935
|
G | A | 4 | a0008c0011t0001g0171a0008c0011t0001g0172a0008c0011t0001g0277others(1): Show | 4 | HG00733.hp2 HG02451.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-25G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 4/31 | chr5 | 176568935 | ||||||
chr5:176569080
|
G | A | 4 | a0004c0010t0001g0016a0004c0010t0001g0017a0004c0010t0001g0032others(1): Show | 6 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+70G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176569080 | ||||||
chr5:176569159
|
T | C | 1 | a0003c0002t0001g0185 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.315+149T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176569159 | ||||||
chr5:176569287
|
G | GT | 137 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(134): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.315+291dupT | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176569287 | |||||
chr5:176569346
|
C | T | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.315+336C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176569346 | ||||||
chr5:176569354
|
G | A | 1 | a0001c0017t0001g0134 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.315+344G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176569354 | ||||||
chr5:176569376
|
T | C | 1 | a0003c0002t0001g0184 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.315+366T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176569376 | ||||||
chr5:176569403
|
C | A | 6 | a0005c0007t0001g0009a0005c0007t0001g0062a0005c0007t0001g0065others(3): Show | 7 | HG00280.hp2 HG02602.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.315+393C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176569403 | ||||||
chr5:176569417
|
G | A | 25 | a0001c0005t0001g0311a0001c0008t0001g0165a0001c0008t0001g0166others(22): Show | 27 | HG00733.hp2 HG02451.hp1 HG02451.hp2 others(24): Show |
intron_variant | MODIFIER | c.315+407G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176569417 | ||||||
chr5:176569432
|
A | C | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.315+422A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176569432 | ||||||
chr5:176569435
|
C | T | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.315+425C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176569435 | ||||||
chr5:176569578
|
G | A | 1 | a0001c0003t0001g0318 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.315+568G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176569578 | ||||||
chr5:176569829
|
A | G | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.315+819A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176569829 | ||||||
chr5:176569908
|
C | T | 7 | a0001c0004t0001g0169a0004c0009t0001g0146a0004c0009t0001g0147others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.315+898C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176569908 | ||||||
chr5:176569959
|
C | CAAAA | 10 | a0003c0002t0001g0184a0003c0002t0001g0219a0003c0002t0001g0241others(7): Show | 11 | HG00323.hp1 HG00733.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.315+959_315+962dup others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176569959 | |||||
chr5:176569959
|
C | CAAAAA | 105 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(102): Show | 110 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+958_315+962dup others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176569959 | |||||
chr5:176569959
|
CA | C | 9 | a0001c0004t0001g0169a0002c0001t0001g0108a0004c0009t0001g0146others(6): Show | 9 | HG01069.hp1 HG01256.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.315+962delA | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176569959 | |||||
chr5:176569986
|
G | A | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.315+976G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176569986 | ||||||
chr5:176570059
|
T | C | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.315+1049T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176570059 | ||||||
chr5:176570065
|
C | T | 1 | a0006c0019t0001g0043 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.315+1055C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176570065 | ||||||
chr5:176570227
|
T | G | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.316-986T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176570227 | ||||||
chr5:176570308
|
C | T | 4 | a0004c0010t0001g0016a0004c0010t0001g0017a0004c0010t0001g0032others(1): Show | 6 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-905C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176570308 | ||||||
chr5:176570320
|
C | T | 8 | a0001c0004t0001g0169a0004c0009t0001g0146a0004c0009t0001g0147others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.316-893C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176570320 | ||||||
chr5:176570328
|
G | A | 2 | a0010c0018t0001g0004a0010c0018t0001g0057 | 3 | HG00642.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.316-885G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176570328 | ||||||
chr5:176570473
|
G | A | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.316-740G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176570473 | ||||||
chr5:176570490
|
C | T | 6 | a0001c0005t0001g0013a0001c0005t0001g0046a0001c0005t0001g0173others(3): Show | 7 | HG02922.hp2 HG03139.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.316-723C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176570490 | ||||||
chr5:176570545
|
C | T | 3 | a0014c0020t0001g0180a0014c0020t0001g0181a0018c0035t0001g0182 | 3 | HG02630.hp2 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.316-668C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176570545 | ||||||
chr5:176570648
|
T | C | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.316-565T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176570648 | ||||||
chr5:176570835
|
C | T | 3 | a0008c0011t0001g0171a0008c0011t0001g0172a0008c0011t0001g0313 | 3 | HG00733.hp2 HG02451.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.316-378C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176570835 | ||||||
chr5:176570865
|
T | C | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.316-348T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176570865 | ||||||
chr5:176570883
|
G | A | 90 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(87): Show | 94 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.316-330G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176570883 | ||||||
chr5:176570932
|
C | T | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.316-281C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176570932 | ||||||
chr5:176570950
|
T | TA | 8 | a0001c0004t0001g0169a0002c0001t0001g0127a0004c0009t0001g0146others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.316-248dupA | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176570950 | |||||
chr5:176570950
|
TA | T | 45 | a0001c0003t0001g0301a0001c0004t0001g0022a0001c0004t0001g0040others(42): Show | 45 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.316-248delA | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176570950 | |||||
chr5:176570950
|
TAA | T | 118 | a0001c0004t0001g0268a0001c0004t0001g0295a0001c0005t0001g0013others(115): Show | 124 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.316-249_316-248del others(2): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176570950 | |||||
chr5:176571037
|
C | CA | 72 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0023others(69): Show | 82 | HG00099.hp2 HG00323.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.316-145dupA | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176571037 | |||||
chr5:176571037
|
C | CAA | 16 | a0001c0003t0001g0021a0001c0003t0001g0047a0001c0003t0001g0048others(13): Show | 18 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.316-146_316-145dup others(2): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176571037 | |||||
chr5:176571037
|
CA | C | 10 | a0001c0004t0001g0179a0001c0004t0001g0265a0001c0004t0001g0279others(7): Show | 12 | HG01109.hp1 HG01255.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.316-145delA | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176571037 | |||||
chr5:176571037
|
CAA | C | 6 | a0002c0001t0001g0026a0002c0001t0001g0092a0002c0001t0001g0119others(3): Show | 6 | HG02572.hp1 HG02717.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-146_316-145del others(2): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176571037 | |||||
chr5:176571037
|
CAAAAAAA others(4): Show |
C | 1 | a0003c0002t0001g0197 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.316-155_316-145del others(11): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176571037 | |||||
chr5:176571037
|
CAAAAAAA others(5): Show |
C | 90 | a0001c0005t0001g0018a0001c0005t0001g0200a0001c0025t0001g0195others(87): Show | 93 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.316-156_316-145del others(12): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176571037 | |||||
chr5:176571037
|
CAAAAAAA others(6): Show |
C | 20 | a0001c0005t0001g0013a0001c0005t0001g0046a0001c0005t0001g0173others(17): Show | 23 | HG02451.hp1 HG02486.hp1 HG02622.hp1 others(20): Show |
intron_variant | MODIFIER | c.316-157_316-145del others(13): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176571037 | |||||
chr5:176571037
|
CAAAAAAA others(7): Show |
C | 6 | a0006c0019t0001g0043a0006c0019t0001g0044a0008c0011t0001g0171others(3): Show | 6 | HG00733.hp2 HG01884.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-158_316-145del others(14): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176571037 | |||||
chr5:176571037
|
CAAAAAAA others(8): Show |
C | 1 | a0002c0001t0001g0093 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.316-159_316-145del others(15): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr5 | 176571037 | |||||
chr5:176571207
|
T | G | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
splice_region_variant&intron_variant | LOW | c.316-6T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 5/31 | chr5 | 176571207 | ||||||
chr5:176571333
|
A | C | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.405+31A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571333 | ||||||
chr5:176571396
|
A | G | 129 | a0001c0004t0001g0169a0001c0005t0001g0013a0001c0005t0001g0018others(126): Show | 136 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.405+94A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571396 | ||||||
chr5:176571465
|
C | CAA | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.405+163_405+164ins others(2): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571465 | ||||||
chr5:176571522
|
C | CA | 4 | a0004c0010t0001g0016a0004c0010t0001g0017a0004c0010t0001g0032others(1): Show | 6 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.405+232dupA | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr5 | 176571522 | |||||
chr5:176571522
|
CA | C | 112 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(109): Show | 118 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.405+232delA | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr5 | 176571522 | |||||
chr5:176571526
|
A | G | 1 | a0004c0009t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.405+224A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571526 | ||||||
chr5:176571551
|
T | C | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.405+249T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571551 | ||||||
chr5:176571622
|
C | T | 4 | a0001c0005t0001g0013a0001c0005t0001g0046a0001c0005t0001g0173others(1): Show | 5 | HG03139.hp2 HG03453.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+320C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571622 | ||||||
chr5:176571629
|
T | C | 1 | a0003c0002t0001g0183 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.405+327T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571629 | ||||||
chr5:176571685
|
C | T | 8 | a0006c0014t0001g0003a0006c0014t0001g0045a0006c0019t0001g0043others(5): Show | 9 | HG00733.hp2 HG01884.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.405+383C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571685 | ||||||
chr5:176571757
|
C | T | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.405+455C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571757 | ||||||
chr5:176571761
|
T | C | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.405+459T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571761 | ||||||
chr5:176571778
|
C | T | 95 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(92): Show | 99 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.405+476C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571778 | ||||||
chr5:176571779
|
G | A | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.405+477G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571779 | ||||||
chr5:176571816
|
G | A | 1 | a0001c0003t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.405+514G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571816 | ||||||
chr5:176571914
|
G | T | 40 | a0001c0003t0001g0301a0001c0004t0001g0022a0001c0004t0001g0040others(37): Show | 40 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.405+612G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571914 | ||||||
chr5:176571934
|
G | A | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.405+632G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176571934 | ||||||
chr5:176572106
|
G | A | 1 | a0001c0003t0001g0301 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.405+804G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572106 | ||||||
chr5:176572112
|
C | T | 7 | a0001c0004t0001g0169a0004c0009t0001g0146a0004c0009t0001g0147others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.405+810C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572112 | ||||||
chr5:176572154
|
T | C | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.405+852T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572154 | ||||||
chr5:176572159
|
G | A | 1 | a0003c0002t0001g0197 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.405+857G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572159 | ||||||
chr5:176572181
|
G | C | 117 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(114): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.405+879G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572181 | ||||||
chr5:176572191
|
C | G | 1 | a0001c0003t0001g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.405+889C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572191 | ||||||
chr5:176572205
|
G | A | 1 | a0001c0013t0001g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.405+903G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572205 | ||||||
chr5:176572222
|
GA | G | 16 | a0001c0003t0001g0104a0001c0004t0001g0169a0001c0004t0001g0260others(13): Show | 17 | HG00423.hp1 HG01255.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.405+936delA | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr5 | 176572222 | |||||
chr5:176572222
|
GAA | G | 113 | a0001c0005t0001g0018a0001c0005t0001g0200a0001c0005t0001g0311others(110): Show | 118 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.405+935_405+936del others(2): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr5 | 176572222 | |||||
chr5:176572244
|
C | T | 1 | a0003c0002t0001g0248 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.405+942C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572244 | ||||||
chr5:176572390
|
A | AAAATAAA others(1): Show |
5 | a0003c0002t0001g0188a0006c0014t0001g0003a0006c0014t0001g0045others(2): Show | 6 | HG01192.hp1 HG02622.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.405+1107_405+1114d others(10): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr5 | 176572390 | |||||
chr5:176572390
|
A | AAAATAAA others(5): Show |
5 | a0001c0005t0001g0013a0001c0005t0001g0173a0001c0005t0001g0296others(2): Show | 6 | HG02280.hp2 HG03139.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.405+1103_405+1114d others(14): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr5 | 176572390 | |||||
chr5:176572390
|
A | AAAATAAA others(9): Show |
81 | a0001c0005t0001g0018a0001c0005t0001g0200a0001c0005t0001g0311others(78): Show | 85 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.405+1099_405+1114d others(18): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr5 | 176572390 | |||||
chr5:176572390
|
A | AAAATAAA others(13): Show |
19 | a0001c0008t0001g0165a0001c0008t0001g0166a0001c0008t0001g0176others(16): Show | 19 | HG00733.hp2 HG02056.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.405+1095_405+1114d others(22): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr5 | 176572390 | |||||
chr5:176572390
|
A | AAAATAAA others(17): Show |
3 | a0003c0002t0001g0186a0008c0011t0001g0171a0012c0021t0001g0037 | 3 | HG03453.hp2 NA19070.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.405+1091_405+1114d others(26): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr5 | 176572390 | |||||
chr5:176572464
|
G | A | 42 | a0001c0003t0001g0301a0001c0004t0001g0022a0001c0004t0001g0040others(39): Show | 42 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.405+1162G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572464 | ||||||
chr5:176572527
|
A | C | 22 | a0001c0005t0001g0311a0001c0016t0001g0014a0001c0016t0001g0137others(19): Show | 24 | HG00733.hp2 HG01884.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.405+1225A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572527 | ||||||
chr5:176572571
|
G | T | 112 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(109): Show | 118 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.405+1269G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572571 | ||||||
chr5:176572707
|
G | A | 1 | a0022c0054t0001g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.406-1376G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572707 | ||||||
chr5:176572710
|
A | G | 4 | a0001c0005t0001g0013a0001c0005t0001g0046a0001c0005t0001g0173others(1): Show | 5 | HG03139.hp2 HG03453.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.406-1373A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572710 | ||||||
chr5:176572734
|
T | A | 2 | a0001c0005t0001g0018a0001c0005t0001g0200 | 3 | HG00140.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.406-1349T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572734 | ||||||
chr5:176572761
|
G | A | 7 | a0001c0004t0001g0169a0004c0009t0001g0146a0004c0009t0001g0147others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.406-1322G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572761 | ||||||
chr5:176572784
|
G | A | 23 | a0001c0005t0001g0013a0001c0005t0001g0046a0001c0005t0001g0173others(20): Show | 26 | HG00733.hp2 HG01884.hp1 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.406-1299G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572784 | ||||||
chr5:176572813
|
G | A | 4 | a0008c0011t0001g0171a0008c0011t0001g0172a0008c0011t0001g0277others(1): Show | 4 | HG00733.hp2 HG02451.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-1270G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572813 | ||||||
chr5:176572973
|
G | A | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.406-1110G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176572973 | ||||||
chr5:176573326
|
C | T | 1 | a0008c0011t0001g0277 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.406-757C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176573326 | ||||||
chr5:176573457
|
C | T | 1 | a0001c0003t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.406-626C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176573457 | ||||||
chr5:176573485
|
T | A | 12 | a0001c0016t0001g0014a0001c0016t0001g0137a0001c0038t0001g0152others(9): Show | 15 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.406-598T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176573485 | ||||||
chr5:176573485
|
T | TA | 104 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(101): Show | 109 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.406-597dupA | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr5 | 176573485 | |||||
chr5:176573487
|
T | A | 119 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(116): Show | 127 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.406-596T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176573487 | ||||||
chr5:176573489
|
T | A | 217 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(214): Show | 232 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.406-594T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176573489 | ||||||
chr5:176573530
|
C | T | 119 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(116): Show | 127 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.406-553C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176573530 | ||||||
chr5:176573649
|
G | GA | 122 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(119): Show | 131 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.406-424dupA | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr5 | 176573649 | |||||
chr5:176573691
|
G | A | 1 | a0002c0026t0001g0201 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.406-392G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176573691 | ||||||
chr5:176573786
|
C | T | 4 | a0001c0004t0001g0022a0001c0004t0001g0270a0001c0044t0001g0022others(1): Show | 4 | HG02071.hp2 HG02155.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.406-297C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176573786 | ||||||
chr5:176573820
|
T | G | 35 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(32): Show | 39 | HG00323.hp2 HG00642.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.406-263T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176573820 | ||||||
chr5:176573850
|
A | T | 1 | a0003c0002t0001g0249 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.406-233A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176573850 | ||||||
chr5:176573921
|
G | A | 6 | a0006c0014t0001g0003a0006c0014t0001g0045a0008c0011t0001g0171others(3): Show | 7 | HG00733.hp2 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.406-162G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176573921 | ||||||
chr5:176573931
|
G | C | 3 | a0014c0020t0001g0180a0014c0020t0001g0181a0018c0035t0001g0182 | 3 | HG02630.hp2 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.406-152G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176573931 | ||||||
chr5:176573985
|
G | C | 7 | a0002c0001t0001g0055a0002c0001t0001g0058a0002c0001t0001g0074others(4): Show | 7 | HG03834.hp2 NA18940.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.406-98G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 6/31 | chr5 | 176573985 | ||||||
chr5:176574188
|
G | A | 92 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(89): Show | 96 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.495+16G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176574188 | ||||||
chr5:176574233
|
C | G | 86 | a0001c0005t0001g0018a0001c0005t0001g0200a0001c0025t0001g0195others(83): Show | 89 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.495+61C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176574233 | ||||||
chr5:176574241
|
A | G | 1 | a0002c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.495+69A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176574241 | ||||||
chr5:176574252
|
G | A | 20 | a0001c0016t0001g0014a0001c0016t0001g0137a0001c0038t0001g0152others(17): Show | 24 | HG00733.hp2 HG01109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.495+80G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176574252 | ||||||
chr5:176574303
|
G | A | 1 | a0001c0003t0001g0308 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.495+131G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176574303 | ||||||
chr5:176574340
|
C | T | 1 | a0002c0001t0001g0093 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.495+168C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176574340 | ||||||
chr5:176574363
|
G | T | 1 | a0002c0001t0001g0081 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.495+191G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176574363 | ||||||
chr5:176574399
|
C | T | 111 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(108): Show | 119 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.495+227C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176574399 | ||||||
chr5:176574434
|
A | G | 1 | a0003c0002t0001g0184 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.495+262A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176574434 | ||||||
chr5:176574475
|
G | A | 3 | a0001c0003t0001g0256a0001c0003t0001g0257a0001c0003t0001g0258 | 3 | HG01109.hp2 HG01255.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.495+303G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176574475 | ||||||
chr5:176574507
|
G | A | 1 | a0022c0054t0001g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.495+335G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176574507 | ||||||
chr5:176574522
|
T | C | 118 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(115): Show | 126 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.495+350T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176574522 | ||||||
chr5:176574974
|
T | C | 264 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(261): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.496-110T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176574974 | ||||||
chr5:176575033
|
T | C | 5 | a0004c0010t0001g0016a0004c0010t0001g0017a0004c0010t0001g0032others(2): Show | 7 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.496-51T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176575033 | ||||||
chr5:176575063
|
C | T | 4 | a0008c0011t0001g0171a0008c0011t0001g0172a0008c0011t0001g0277others(1): Show | 4 | HG00733.hp2 HG02451.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-21C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 7/31 | chr5 | 176575063 | ||||||
chr5:176575636
|
C | T | 1 | a0002c0001t0001g0151 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.844+55C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 10/31 | chr5 | 176575636 | ||||||
chr5:176575637
|
G | A | 1 | a0002c0001t0001g0115 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.844+56G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 10/31 | chr5 | 176575637 | ||||||
chr5:176575706
|
C | T | 45 | a0001c0004t0001g0022a0001c0004t0001g0040a0001c0004t0001g0059others(42): Show | 46 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.845-18C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 10/31 | chr5 | 176575706 | ||||||
chr5:176575872
|
C | T | 245 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(242): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.960+33C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 11/31 | chr5 | 176575872 | ||||||
chr5:176575925
|
C | A | 242 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(239): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.961-27C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 11/31 | chr5 | 176575925 | ||||||
chr5:176576192
|
G | A | 1 | a0003c0012t0001g0086 | 1 | HG00733.hp1 | splice_region_variant&intron_variant | LOW | c.1194+7G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576192 | ||||||
chr5:176576199
|
C | T | 5 | a0004c0010t0001g0016a0004c0010t0001g0017a0004c0010t0001g0032others(2): Show | 7 | HG01109.hp1 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1194+14C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576199 | ||||||
chr5:176576212
|
G | A | 5 | a0001c0006t0001g0170a0002c0001t0001g0038a0002c0052t0001g0155others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1194+27G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576212 | ||||||
chr5:176576305
|
G | A | 3 | a0014c0020t0001g0180a0014c0020t0001g0181a0018c0035t0001g0182 | 3 | HG02630.hp2 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1194+120G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576305 | ||||||
chr5:176576366
|
G | A | 104 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(101): Show | 110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1194+181G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576366 | ||||||
chr5:176576421
|
C | A | 27 | a0001c0004t0001g0059a0001c0004t0001g0169a0001c0004t0001g0179others(24): Show | 28 | HG00280.hp1 HG00423.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1194+236C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576421 | ||||||
chr5:176576422
|
G | A | 10 | a0001c0006t0001g0141a0002c0001t0001g0015a0002c0001t0001g0140others(7): Show | 11 | HG00099.hp2 HG00735.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1194+237G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576422 | ||||||
chr5:176576453
|
C | T | 267 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(264): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1194+268C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576453 | ||||||
chr5:176576490
|
G | A | 2 | a0013c0022t0001g0261a0013c0022t0001g0262 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1194+305G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576490 | ||||||
chr5:176576579
|
CT | C | 216 | a0001c0004t0001g0267a0001c0004t0001g0299a0001c0005t0001g0013others(213): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1194+409delT | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr5 | 176576579 | |||||
chr5:176576652
|
C | A | 110 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(107): Show | 117 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1194+467C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576652 | ||||||
chr5:176576652
|
C | G | 1 | a0001c0038t0001g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1194+467C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576652 | ||||||
chr5:176576674
|
G | T | 265 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(262): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1194+489G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576674 | ||||||
chr5:176576714
|
T | C | 265 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(262): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1194+529T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576714 | ||||||
chr5:176576866
|
C | T | 1 | a0003c0002t0001g0241 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1195-533C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576866 | ||||||
chr5:176576930
|
G | A | 1 | a0002c0001t0001g0028 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1195-469G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576930 | ||||||
chr5:176576953
|
G | A | 92 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(89): Show | 96 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.1195-446G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576953 | ||||||
chr5:176576959
|
A | G | 264 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(261): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1195-440A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576959 | ||||||
chr5:176576966
|
T | C | 308 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(305): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1195-433T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176576966 | ||||||
chr5:176577116
|
G | A | 258 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(255): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1195-283G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176577116 | ||||||
chr5:176577125
|
G | C | 10 | a0001c0006t0001g0170a0001c0008t0001g0165a0001c0008t0001g0166others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1195-274G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176577125 | ||||||
chr5:176577134
|
C | T | 258 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(255): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1195-265C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176577134 | ||||||
chr5:176577211
|
A | C | 303 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(300): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1195-188A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176577211 | ||||||
chr5:176577311
|
A | G | 318 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(315): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1195-88A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176577311 | ||||||
chr5:176577324
|
A | G | 2 | a0015c0024t0001g0071a0015c0024t0001g0073 | 2 | NA19079.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1195-75A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176577324 | ||||||
chr5:176577383
|
C | T | 1 | a0003c0002t0001g0217 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1195-16C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 12/31 | chr5 | 176577383 | ||||||
chr5:176577582
|
C | T | 5 | a0006c0014t0001g0003a0006c0014t0001g0045a0014c0020t0001g0180others(2): Show | 6 | HG02622.hp1 HG02630.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1350+28C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 13/31 | chr5 | 176577582 | ||||||
chr5:176577845
|
C | T | 256 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(253): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1512+47C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 14/31 | chr5 | 176577845 | ||||||
chr5:176577865
|
A | AGT | 243 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(240): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1512+80_1512+81dup others(2): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr5 | 176577865 | |||||
chr5:176577865
|
A | AGTGT | 10 | a0001c0006t0001g0170a0001c0008t0001g0165a0001c0008t0001g0166others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1512+78_1512+81dup others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr5 | 176577865 | |||||
chr5:176577867
|
T | A | 6 | a0005c0007t0001g0009a0005c0007t0001g0062a0005c0007t0001g0065others(3): Show | 7 | HG00280.hp2 HG02602.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1512+69T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 14/31 | chr5 | 176577867 | ||||||
chr5:176577902
|
T | C | 39 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(36): Show | 45 | HG00323.hp2 HG00642.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1512+104T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 14/31 | chr5 | 176577902 | ||||||
chr5:176577960
|
G | A | 3 | a0014c0020t0001g0180a0014c0020t0001g0181a0018c0035t0001g0182 | 3 | HG02630.hp2 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1513-74G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 14/31 | chr5 | 176577960 | ||||||
chr5:176577967
|
C | G | 1 | a0012c0021t0001g0314 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1513-67C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 14/31 | chr5 | 176577967 | ||||||
chr5:176577968
|
G | A | 1 | a0012c0021t0001g0314 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1513-66G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 14/31 | chr5 | 176577968 | ||||||
chr5:176578116
|
G | C | 2 | a0003c0002t0001g0202a0003c0002t0001g0203 | 2 | NA18951.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1574+21G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 15/31 | chr5 | 176578116 | ||||||
chr5:176578174
|
A | C | 145 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(142): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1574+79A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 15/31 | chr5 | 176578174 | ||||||
chr5:176578183
|
G | A | 201 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(198): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1574+88G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 15/31 | chr5 | 176578183 | ||||||
chr5:176578194
|
G | T | 4 | a0003c0002t0001g0188a0003c0002t0001g0189a0003c0002t0001g0191others(1): Show | 4 | HG01168.hp1 HG01192.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1574+99G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 15/31 | chr5 | 176578194 | ||||||
chr5:176578636
|
A | G | 6 | a0006c0014t0001g0003a0006c0014t0001g0045a0008c0011t0001g0171others(3): Show | 7 | HG00733.hp2 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1818+28A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176578636 | ||||||
chr5:176578767
|
C | T | 1 | a0003c0033t0001g0112 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1818+159C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176578767 | ||||||
chr5:176578826
|
G | A | 6 | a0005c0007t0001g0009a0005c0007t0001g0062a0005c0007t0001g0065others(3): Show | 7 | HG00280.hp2 HG02602.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1818+218G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176578826 | ||||||
chr5:176578874
|
C | A | 1 | a0002c0001t0001g0063 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1818+266C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176578874 | ||||||
chr5:176579090
|
C | A | 4 | a0001c0004t0001g0022a0001c0004t0001g0270a0001c0044t0001g0022others(1): Show | 4 | HG02071.hp2 HG02155.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.1818+482C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176579090 | ||||||
chr5:176579148
|
G | A | 1 | a0002c0001t0001g0025 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1818+540G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176579148 | ||||||
chr5:176579420
|
G | A | 3 | a0014c0020t0001g0180a0014c0020t0001g0181a0018c0035t0001g0182 | 3 | HG02630.hp2 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1818+812G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176579420 | ||||||
chr5:176579442
|
C | T | 1 | a0001c0004t0001g0059 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1818+834C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176579442 | ||||||
chr5:176579468
|
C | T | 1 | a0001c0004t0001g0285 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1818+860C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176579468 | ||||||
chr5:176579515
|
C | A | 6 | a0005c0007t0001g0009a0005c0007t0001g0062a0005c0007t0001g0065others(3): Show | 7 | HG00280.hp2 HG02602.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1818+907C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176579515 | ||||||
chr5:176579569
|
G | A | 103 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(100): Show | 109 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1818+961G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176579569 | ||||||
chr5:176579610
|
A | G | 100 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(97): Show | 106 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1818+1002A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176579610 | ||||||
chr5:176579698
|
G | T | 1 | a0002c0001t0001g0151 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1818+1090G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176579698 | ||||||
chr5:176579867
|
G | A | 8 | a0004c0010t0001g0016a0004c0010t0001g0017a0004c0010t0001g0032others(5): Show | 10 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1818+1259G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176579867 | ||||||
chr5:176579909
|
C | A | 1 | a0002c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1818+1301C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176579909 | ||||||
chr5:176580119
|
C | G | 2 | a0006c0014t0001g0003a0006c0014t0001g0045 | 3 | HG02622.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1819-1224C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176580119 | ||||||
chr5:176580142
|
G | GCACTCAC others(5): Show |
100 | a0001c0006t0001g0011a0001c0006t0001g0110a0001c0006t0001g0111others(97): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.1819-1189_1819-117 others(16): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr5 | 176580142 | |||||
chr5:176580147
|
C | T | 1 | a0001c0004t0002g0276 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1819-1196C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176580147 | ||||||
chr5:176580148
|
ACACACAC others(15): Show |
A | 4 | a0001c0005t0001g0013a0001c0005t0001g0046a0001c0005t0001g0173others(1): Show | 5 | HG03139.hp2 HG03453.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1819-1168_1819-114 others(26): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr5 | 176580148 | |||||
chr5:176580528
|
C | CA | 110 | a0001c0003t0001g0101a0001c0004t0001g0022a0001c0004t0001g0270others(107): Show | 116 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.1819-800dupA | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr5 | 176580528 | |||||
chr5:176580528
|
C | CAA | 7 | a0001c0003t0001g0010a0001c0003t0001g0098a0001c0003t0001g0099others(4): Show | 8 | HG01074.hp2 HG01175.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1819-801_1819-800d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr5 | 176580528 | |||||
chr5:176580551
|
A | C | 1 | a0001c0013t0001g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1819-792A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176580551 | ||||||
chr5:176580608
|
C | T | 1 | a0003c0002t0001g0241 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1819-735C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176580608 | ||||||
chr5:176580983
|
T | TTGAA | 161 | a0001c0004t0001g0022a0001c0004t0001g0040a0001c0004t0001g0059others(158): Show | 170 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1819-358_1819-357i others(6): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr5 | 176580983 | |||||
chr5:176581005
|
A | G | 47 | a0001c0004t0001g0022a0001c0004t0001g0040a0001c0004t0001g0059others(44): Show | 49 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1819-338A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176581005 | ||||||
chr5:176581008
|
TC | T | 47 | a0001c0004t0001g0022a0001c0004t0001g0040a0001c0004t0001g0059others(44): Show | 49 | HG00280.hp1 HG00423.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1819-330delC | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr5 | 176581008 | |||||
chr5:176581124
|
T | C | 1 | a0012c0021t0001g0314 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1819-219T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176581124 | ||||||
chr5:176581149
|
A | G | 1 | a0001c0013t0001g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1819-194A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176581149 | ||||||
chr5:176581189
|
G | A | 90 | a0001c0004t0001g0290a0001c0005t0001g0013a0001c0005t0001g0046others(87): Show | 93 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1819-154G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176581189 | ||||||
chr5:176581237
|
G | T | 229 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(226): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1819-106G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176581237 | ||||||
chr5:176581257
|
G | A | 1 | a0001c0038t0001g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1819-86G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 16/31 | chr5 | 176581257 | ||||||
chr5:176581593
|
G | A | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2058+11G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176581593 | ||||||
chr5:176581627
|
C | T | 1 | a0001c0005t0001g0311 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2058+45C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176581627 | ||||||
chr5:176581630
|
T | C | 2 | a0003c0002t0001g0198a0003c0002t0001g0205 | 2 | HG02040.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.2058+48T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176581630 | ||||||
chr5:176581647
|
T | C | 1 | a0002c0001t0001g0158 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2058+65T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176581647 | ||||||
chr5:176581863
|
G | A | 2 | a0001c0005t0001g0311a0001c0038t0001g0152 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2058+281G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176581863 | ||||||
chr5:176581955
|
A | T | 3 | a0001c0048t0001g0315a0007c0031t0001g0316a0007c0031t0001g0317 | 3 | HG01891.hp2 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2058+373A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176581955 | ||||||
chr5:176581964
|
C | T | 3 | a0014c0020t0001g0180a0014c0020t0001g0181a0018c0035t0001g0182 | 3 | HG02630.hp2 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2058+382C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176581964 | ||||||
chr5:176582136
|
T | TCAGCCTC others(13): Show |
1 | a0003c0002t0001g0187 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2058+555_2058+574d others(22): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr5 | 176582136 | |||||
chr5:176582356
|
T | A | 298 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(295): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.2058+774T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176582356 | ||||||
chr5:176582426
|
A | G | 1 | a0003c0002t0001g0215 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2058+844A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176582426 | ||||||
chr5:176582457
|
TG | T | 91 | a0001c0006t0001g0011a0001c0006t0001g0110a0001c0006t0001g0111others(88): Show | 94 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2058+876delG | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176582457 | ||||||
chr5:176582475
|
G | A | 161 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(158): Show | 175 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.2058+893G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176582475 | ||||||
chr5:176582528
|
A | G | 1 | a0002c0001t0001g0125 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2058+946A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176582528 | ||||||
chr5:176582723
|
G | A | 161 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(158): Show | 175 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.2058+1141G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176582723 | ||||||
chr5:176582766
|
A | G | 1 | a0001c0004t0001g0289 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2058+1184A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176582766 | ||||||
chr5:176582881
|
C | T | 4 | a0001c0038t0001g0152a0001c0041t0001g0264a0006c0019t0001g0043others(1): Show | 4 | HG01884.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2058+1299C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176582881 | ||||||
chr5:176583124
|
A | C | 76 | a0001c0004t0001g0040a0001c0004t0001g0179a0001c0004t0001g0265others(73): Show | 78 | HG00323.hp1 HG00639.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.2059-1066A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176583124 | ||||||
chr5:176583155
|
G | T | 83 | a0001c0004t0001g0273a0001c0006t0001g0011a0001c0006t0001g0110others(80): Show | 87 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.2059-1035G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176583155 | ||||||
chr5:176583169
|
G | A | 1 | a0003c0002t0001g0207 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2059-1021G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176583169 | ||||||
chr5:176583304
|
C | T | 2 | a0001c0004t0001g0169a0001c0004t0001g0295 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2059-886C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176583304 | ||||||
chr5:176583365
|
C | A | 1 | a0015c0024t0001g0071 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2059-825C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176583365 | ||||||
chr5:176583549
|
G | A | 1 | a0001c0004t0001g0286 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2059-641G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176583549 | ||||||
chr5:176583706
|
C | T | 1 | a0003c0002t0001g0255 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2059-484C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176583706 | ||||||
chr5:176583735
|
G | A | 1 | a0003c0002t0001g0228 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2059-455G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176583735 | ||||||
chr5:176583787
|
C | G | 21 | a0001c0005t0001g0311a0001c0006t0001g0141a0001c0006t0001g0170others(18): Show | 23 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.2059-403C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176583787 | ||||||
chr5:176583890
|
T | TCTAGAAA others(46): Show |
1 | a0002c0001t0001g0069 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2059-298_2059-246d others(55): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr5 | 176583890 | |||||
chr5:176584162
|
G | A | 2 | a0001c0004t0001g0268a0001c0004t0001g0274 | 2 | NA18939.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2059-28G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 17/31 | chr5 | 176584162 | ||||||
chr5:176584263
|
T | C | 171 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(168): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
splice_region_variant&intron_variant | LOW | c.2128+4T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 18/31 | chr5 | 176584263 | ||||||
chr5:176585064
|
C | A | 3 | a0007c0027t0001g0035a0007c0027t0001g0036a0022c0054t0001g0175 | 3 | HG02922.hp2 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2734+49C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585064 | ||||||
chr5:176585066
|
C | T | 97 | a0001c0006t0001g0233a0001c0017t0001g0134a0001c0017t0001g0135others(94): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.2734+51C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585066 | ||||||
chr5:176585082
|
G | T | 2 | a0001c0013t0001g0029a0001c0048t0001g0315 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2734+67G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585082 | ||||||
chr5:176585226
|
A | G | 5 | a0001c0006t0001g0011a0001c0006t0001g0110a0001c0006t0001g0111others(2): Show | 6 | HG01928.hp1 HG02132.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.2734+211A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585226 | ||||||
chr5:176585293
|
AT | A | 96 | a0001c0006t0001g0233a0001c0017t0001g0134a0001c0017t0001g0135others(93): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.2734+282delT | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr5 | 176585293 | |||||
chr5:176585303
|
A | G | 2 | a0001c0003t0001g0107a0001c0003t0001g0163 | 2 | HG01928.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2734+288A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585303 | ||||||
chr5:176585351
|
C | T | 4 | a0001c0005t0001g0311a0001c0041t0001g0264a0006c0019t0001g0043others(1): Show | 4 | HG01884.hp1 HG02486.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2734+336C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585351 | ||||||
chr5:176585490
|
A | G | 96 | a0001c0006t0001g0233a0001c0017t0001g0134a0001c0017t0001g0135others(93): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.2735-464A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585490 | ||||||
chr5:176585676
|
T | G | 1 | a0003c0002t0001g0187 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2735-278T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585676 | ||||||
chr5:176585677
|
C | T | 1 | a0003c0002t0001g0187 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2735-277C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585677 | ||||||
chr5:176585682
|
C | G | 1 | a0003c0002t0001g0187 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2735-272C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585682 | ||||||
chr5:176585685
|
C | G | 1 | a0003c0002t0001g0187 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2735-269C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585685 | ||||||
chr5:176585688
|
A | AGGGCAGG others(4): Show |
1 | a0003c0002t0001g0187 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2735-264_2735-263i others(13): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | INFO_REALIGN_3_PRIME | chr5 | 176585688 | |||||
chr5:176585767
|
G | C | 1 | a0003c0002t0001g0187 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2735-187G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585767 | ||||||
chr5:176585770
|
GCGGGGCA others(28): Show |
G | 1 | a0003c0002t0001g0187 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2735-183_2735-149d others(37): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585770 | ||||||
chr5:176585799
|
C | T | 121 | a0001c0005t0001g0311a0001c0006t0001g0141a0001c0006t0001g0170others(118): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2735-155C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585799 | ||||||
chr5:176585807
|
A | G | 1 | a0003c0002t0001g0187 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2735-147A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585807 | ||||||
chr5:176585808
|
G | A | 1 | a0003c0002t0001g0187 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2735-146G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585808 | ||||||
chr5:176585814
|
G | A | 5 | a0003c0002t0001g0224a0003c0002t0001g0228a0003c0002t0001g0229others(2): Show | 5 | HG02083.hp1 HG02165.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.2735-140G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585814 | ||||||
chr5:176585821
|
A | G | 1 | a0003c0002t0001g0187 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2735-133A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585821 | ||||||
chr5:176585841
|
C | T | 6 | a0001c0006t0001g0141a0001c0006t0001g0170a0004c0039t0001g0024others(3): Show | 6 | HG01109.hp1 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2735-113C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585841 | ||||||
chr5:176585842
|
G | A | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2735-112G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585842 | ||||||
chr5:176585855
|
C | T | 2 | a0001c0016t0001g0014a0001c0016t0001g0137 | 3 | HG02965.hp2 HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2735-99C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585855 | ||||||
chr5:176585856
|
G | A | 1 | a0002c0001t0001g0149 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2735-98G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 19/31 | chr5 | 176585856 | ||||||
chr5:176586064
|
C | T | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2806+39C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 20/31 | chr5 | 176586064 | ||||||
chr5:176586072
|
C | T | 2 | a0001c0004t0001g0268a0001c0004t0001g0274 | 2 | NA18939.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2806+47C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 20/31 | chr5 | 176586072 | ||||||
chr5:176586088
|
C | T | 3 | a0003c0002t0001g0189a0003c0002t0001g0191a0003c0045t0001g0041 | 3 | HG01168.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2806+63C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 20/31 | chr5 | 176586088 | ||||||
chr5:176586117
|
G | A | 5 | a0001c0006t0001g0141a0001c0006t0001g0170a0004c0055t0001g0033others(2): Show | 5 | HG01109.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2806+92G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 20/31 | chr5 | 176586117 | ||||||
chr5:176586208
|
T | C | 2 | a0001c0003t0001g0107a0001c0003t0001g0163 | 2 | HG01928.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2806+183T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 20/31 | chr5 | 176586208 | ||||||
chr5:176586234
|
C | T | 1 | a0004c0039t0001g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2806+209C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 20/31 | chr5 | 176586234 | ||||||
chr5:176586259
|
G | A | 3 | a0001c0005t0001g0013a0001c0005t0001g0173a0001c0005t0001g0296 | 4 | HG03139.hp2 HG03453.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2806+234G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 20/31 | chr5 | 176586259 | ||||||
chr5:176586345
|
G | A | 1 | a0005c0007t0001g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2806+320G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 20/31 | chr5 | 176586345 | ||||||
chr5:176586358
|
G | A | 1 | a0003c0002t0001g0241 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2806+333G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 20/31 | chr5 | 176586358 | ||||||
chr5:176586395
|
T | C | 162 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(159): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.2806+370T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 20/31 | chr5 | 176586395 | ||||||
chr5:176586396
|
G | A | 1 | a0002c0023t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2806+371G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 20/31 | chr5 | 176586396 | ||||||
chr5:176586763
|
C | T | 3 | a0001c0017t0001g0144a0004c0010t0001g0016a0004c0010t0001g0017 | 5 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2807-30C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 20/31 | chr5 | 176586763 | ||||||
chr5:176586789
|
G | A | 5 | a0007c0027t0001g0035a0007c0027t0001g0036a0007c0031t0001g0316others(2): Show | 5 | HG02717.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2807-4G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 20/31 | chr5 | 176586789 | ||||||
chr5:176587047
|
G | A | 15 | a0001c0005t0001g0311a0001c0006t0001g0141a0001c0006t0001g0170others(12): Show | 15 | HG02055.hp1 HG02486.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.2856+205G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587047 | ||||||
chr5:176587125
|
A | C | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2856+283A>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587125 | ||||||
chr5:176587133
|
C | CCAGTGCC others(46): Show |
1 | a0020c0051t0001g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2856+331_2856+332i others(55): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176587133 | |||||
chr5:176587137
|
T | C | 3 | a0002c0001t0001g0132a0002c0001t0001g0133a0002c0053t0001g0131 | 3 | HG01167.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2856+295T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587137 | ||||||
chr5:176587144
|
T | C | 5 | a0003c0002t0001g0224a0003c0002t0001g0228a0003c0002t0001g0229others(2): Show | 5 | HG02083.hp1 HG02165.hp2 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.2856+302T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587144 | ||||||
chr5:176587151
|
A | ATAATTCT others(37): Show |
1 | a0002c0001t0001g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2856+331_2856+332i others(46): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176587151 | |||||
chr5:176587173
|
C | T | 2 | a0001c0013t0001g0029a0001c0048t0001g0315 | 2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2856+331C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587173 | ||||||
chr5:176587174
|
A | G | 173 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(170): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2856+332A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587174 | ||||||
chr5:176587357
|
A | G | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2856+515A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587357 | ||||||
chr5:176587388
|
C | G | 12 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(9): Show | 15 | HG00140.hp1 HG00280.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2856+546C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587388 | ||||||
chr5:176587454
|
A | T | 26 | a0001c0004t0001g0290a0001c0005t0001g0013a0001c0005t0001g0018others(23): Show | 31 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.2856+612A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587454 | ||||||
chr5:176587458
|
T | A | 176 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(173): Show | 188 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2856+616T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587458 | ||||||
chr5:176587462
|
T | A | 7 | a0001c0003t0001g0047a0001c0003t0001g0301a0001c0017t0001g0134others(4): Show | 7 | HG01361.hp1 HG01496.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2856+620T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587462 | ||||||
chr5:176587463
|
A | T | 3 | a0001c0017t0001g0134a0001c0017t0001g0135a0001c0017t0001g0144 | 3 | HG02976.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2856+621A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587463 | ||||||
chr5:176587506
|
C | T | 3 | a0001c0017t0001g0134a0001c0017t0001g0135a0001c0017t0001g0144 | 3 | HG02976.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2856+664C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587506 | ||||||
chr5:176587652
|
C | A | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2856+810C>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587652 | ||||||
chr5:176587653
|
C | G | 4 | a0001c0005t0001g0013a0001c0005t0001g0046a0001c0005t0001g0173others(1): Show | 5 | HG03139.hp2 HG03453.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2856+811C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587653 | ||||||
chr5:176587737
|
A | T | 2 | a0001c0004t0001g0179a0001c0047t0001g0174 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2856+895A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587737 | ||||||
chr5:176587768
|
C | T | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2856+926C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176587768 | ||||||
chr5:176588012
|
G | A | 15 | a0001c0005t0001g0311a0001c0006t0001g0141a0001c0006t0001g0170others(12): Show | 15 | HG02055.hp1 HG02486.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.2857-1019G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588012 | ||||||
chr5:176588111
|
T | C | 3 | a0001c0017t0001g0134a0001c0017t0001g0135a0001c0017t0001g0144 | 3 | HG02976.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2857-920T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588111 | ||||||
chr5:176588115
|
C | G | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2857-916C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588115 | ||||||
chr5:176588203
|
AGT | A | 110 | a0001c0005t0001g0311a0001c0006t0001g0141a0001c0006t0001g0170others(107): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.2857-817_2857-816d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588203 | |||||
chr5:176588282
|
CAG | C | 37 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(34): Show | 41 | HG00323.hp2 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.2857-748_2857-747d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588282 | ||||||
chr5:176588307
|
T | C | 1 | a0001c0003t0001g0101 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2857-724T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588307 | ||||||
chr5:176588333
|
AGT | A | 15 | a0001c0005t0001g0311a0001c0006t0001g0141a0001c0006t0001g0170others(12): Show | 15 | HG02055.hp1 HG02486.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.2857-692_2857-691d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588333 | |||||
chr5:176588363
|
T | TTG | 109 | a0001c0006t0001g0141a0001c0006t0001g0170a0001c0006t0001g0233others(106): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.2857-663_2857-662d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588363 | |||||
chr5:176588366
|
TGTGA | T | 3 | a0004c0010t0001g0016a0004c0010t0001g0017a0004c0010t0001g0032 | 5 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2857-661_2857-658d others(6): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588366 | |||||
chr5:176588370
|
A | T | 1 | a0001c0005t0001g0311 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2857-661A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588370 | ||||||
chr5:176588372
|
T | A | 1 | a0001c0005t0001g0311 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2857-659T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588372 | ||||||
chr5:176588385
|
AGT | A | 12 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(9): Show | 15 | HG00140.hp1 HG00280.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.2857-640_2857-639d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588385 | |||||
chr5:176588406
|
A | T | 95 | a0001c0006t0001g0233a0001c0017t0001g0144a0002c0001t0001g0001others(92): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2857-625A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588406 | ||||||
chr5:176588408
|
A | AGGGT | 95 | a0001c0006t0001g0233a0001c0017t0001g0144a0002c0001t0001g0001others(92): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2857-622_2857-621i others(6): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588408 | |||||
chr5:176588408
|
A | G | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2857-623A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588408 | ||||||
chr5:176588414
|
G | T | 96 | a0001c0006t0001g0233a0001c0017t0001g0144a0002c0001t0001g0001others(93): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.2857-617G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588414 | ||||||
chr5:176588415
|
G | GTA | 95 | a0001c0006t0001g0233a0001c0017t0001g0144a0002c0001t0001g0001others(92): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2857-615_2857-614i others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588415 | |||||
chr5:176588415
|
G | GTGTGAGT others(3): Show |
14 | a0001c0005t0001g0311a0001c0006t0001g0141a0001c0006t0001g0170others(11): Show | 14 | HG02055.hp1 HG02486.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.2857-607_2857-606i others(12): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588415 | |||||
chr5:176588417
|
G | A | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2857-614G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588417 | ||||||
chr5:176588420
|
A | T | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2857-611A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588420 | ||||||
chr5:176588420
|
AGT | A | 40 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(37): Show | 44 | HG00323.hp2 HG00642.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.2857-602_2857-601d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588420 | |||||
chr5:176588422
|
T | A | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2857-609T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588422 | ||||||
chr5:176588448
|
T | G | 1 | a0001c0003t0001g0160 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2857-583T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588448 | ||||||
chr5:176588450
|
TGA | T | 149 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(146): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2857-577_2857-576d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588450 | |||||
chr5:176588472
|
T | TGA | 107 | a0001c0005t0001g0311a0001c0006t0001g0141a0001c0006t0001g0170others(104): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.2857-557_2857-556d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588472 | |||||
chr5:176588475
|
G | GAA | 3 | a0007c0031t0001g0316a0007c0031t0001g0317a0007c0050t0001g0136 | 3 | HG02055.hp1 HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2857-556_2857-555i others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588475 | ||||||
chr5:176588508
|
A | AGT | 109 | a0001c0005t0001g0311a0001c0006t0001g0141a0001c0006t0001g0170others(106): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.2857-517_2857-516d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588508 | |||||
chr5:176588516
|
C | T | 1 | a0002c0001t0001g0133 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2857-515C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588516 | ||||||
chr5:176588516
|
CAT | C | 8 | a0001c0005t0001g0018a0001c0005t0001g0200a0005c0007t0001g0009others(5): Show | 10 | HG00140.hp1 HG00280.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.2857-514_2857-513d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588516 | ||||||
chr5:176588528
|
T | C | 1 | a0003c0002t0001g0245 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2857-503T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588528 | ||||||
chr5:176588538
|
T | TGA | 110 | a0001c0005t0001g0311a0001c0006t0001g0141a0001c0006t0001g0170others(107): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.2857-491_2857-490d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588538 | |||||
chr5:176588574
|
AGT | A | 18 | a0001c0004t0001g0169a0001c0005t0001g0311a0001c0006t0001g0141others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.2857-449_2857-448d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588574 | |||||
chr5:176588576
|
T | A | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2857-455T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588576 | ||||||
chr5:176588589
|
G | A | 9 | a0001c0008t0001g0165a0001c0008t0001g0166a0001c0008t0001g0176others(6): Show | 11 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.2857-442G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588589 | ||||||
chr5:176588596
|
A | AGT | 101 | a0001c0005t0001g0311a0001c0006t0001g0233a0001c0017t0001g0134others(98): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.2857-427_2857-426d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588596 | |||||
chr5:176588596
|
A | T | 4 | a0002c0001t0001g0038a0002c0052t0001g0155a0011c0028t0001g0145others(1): Show | 4 | HG02109.hp1 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2857-435A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588596 | ||||||
chr5:176588637
|
C | CTG | 94 | a0001c0006t0001g0233a0002c0001t0001g0001a0002c0001t0001g0005others(91): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.2857-393_2857-392d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588637 | |||||
chr5:176588637
|
C | CTGTG | 74 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(71): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.2857-392_2857-391i others(6): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588637 | |||||
chr5:176588656
|
T | C | 5 | a0001c0006t0001g0141a0001c0006t0001g0170a0004c0039t0001g0024others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2857-375T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588656 | ||||||
chr5:176588664
|
AGT | A | 3 | a0001c0004t0001g0169a0014c0020t0001g0180a0014c0020t0001g0181 | 3 | HG01884.hp2 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2857-355_2857-354d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588664 | |||||
chr5:176588712
|
A | AGT | 8 | a0001c0008t0001g0165a0001c0008t0001g0166a0001c0008t0001g0176others(5): Show | 10 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.2857-307_2857-306d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588712 | |||||
chr5:176588722
|
T | TGA | 3 | a0001c0017t0001g0134a0001c0017t0001g0135a0001c0017t0001g0144 | 3 | HG02976.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2857-308_2857-307i others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588722 | |||||
chr5:176588724
|
T | A | 3 | a0001c0017t0001g0134a0001c0017t0001g0135a0001c0017t0001g0144 | 3 | HG02976.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2857-307T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588724 | ||||||
chr5:176588724
|
T | TGA | 153 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(150): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.2857-293_2857-292d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588724 | |||||
chr5:176588724
|
T | TGTGA | 3 | a0001c0041t0001g0264a0006c0019t0001g0043a0006c0019t0001g0044 | 3 | HG01884.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2857-306_2857-305i others(6): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588724 | |||||
chr5:176588724
|
TGA | T | 4 | a0002c0001t0001g0158a0003c0002t0001g0207a0003c0002t0001g0210others(1): Show | 4 | HG02723.hp1 HG02738.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.2857-293_2857-292d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588724 | |||||
chr5:176588726
|
A | T | 1 | a0004c0042t0001g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2857-305A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588726 | ||||||
chr5:176588734
|
A | AGAGAGAG others(31): Show |
1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2857-292_2857-291i others(40): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr5 | 176588734 | |||||
chr5:176588770
|
G | A | 3 | a0001c0004t0001g0022a0001c0004t0001g0270a0001c0044t0001g0022 | 3 | HG02071.hp2 HG02155.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.2857-261G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588770 | ||||||
chr5:176588814
|
G | A | 174 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(171): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.2857-217G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588814 | ||||||
chr5:176588940
|
C | T | 1 | a0003c0002t0001g0231 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2857-91C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588940 | ||||||
chr5:176588994
|
G | A | 1 | a0002c0001t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2857-37G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 21/31 | chr5 | 176588994 | ||||||
chr5:176589197
|
C | T | 7 | a0002c0001t0001g0052a0007c0027t0001g0035a0007c0027t0001g0036others(4): Show | 7 | HG02055.hp1 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3008+15C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 22/31 | chr5 | 176589197 | ||||||
chr5:176589273
|
G | C | 3 | a0001c0017t0001g0134a0001c0017t0001g0135a0001c0017t0001g0144 | 3 | HG02976.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3009-57G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 22/31 | chr5 | 176589273 | ||||||
chr5:176589643
|
G | A | 1 | a0003c0002t0001g0072 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3206+27G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 24/31 | chr5 | 176589643 | ||||||
chr5:176589650
|
A | AAGAACAG others(46): Show |
1 | a0001c0003t0001g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3206+36_3206+88dup others(53): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 24/31 | INFO_REALIGN_3_PRIME | chr5 | 176589650 | |||||
chr5:176589730
|
C | T | 1 | a0001c0004t0001g0272 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3206+114C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 24/31 | chr5 | 176589730 | ||||||
chr5:176589821
|
T | C | 154 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(151): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.3206+205T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 24/31 | chr5 | 176589821 | ||||||
chr5:176589859
|
T | C | 9 | a0001c0008t0001g0165a0001c0008t0001g0166a0001c0008t0001g0176others(6): Show | 11 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.3207-219T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 24/31 | chr5 | 176589859 | ||||||
chr5:176589977
|
T | TGCCCTTT others(46): Show |
1 | a0001c0003t0001g0047 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3207-96_3207-44dup others(53): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 24/31 | INFO_REALIGN_3_PRIME | chr5 | 176589977 | |||||
chr5:176590244
|
C | T | 1 | a0003c0002t0001g0219 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3276-9C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 25/31 | chr5 | 176590244 | ||||||
chr5:176590502
|
C | T | 3 | a0001c0004t0001g0022a0001c0004t0001g0270a0001c0044t0001g0022 | 3 | HG02071.hp2 HG02155.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.3414+17C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 27/31 | chr5 | 176590502 | ||||||
chr5:176590548
|
C | T | 51 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(48): Show | 58 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.3415-15C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 27/31 | chr5 | 176590548 | ||||||
chr5:176590692
|
G | A | 1 | a0003c0002t0001g0240 | 1 | HG01981.hp1 | splice_region_variant&intron_variant | LOW | c.3539+5G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 28/31 | chr5 | 176590692 | ||||||
chr5:176590744
|
C | T | 1 | a0003c0002t0001g0203 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3539+57C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 28/31 | chr5 | 176590744 | ||||||
chr5:176590745
|
G | A | 12 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(9): Show | 15 | HG00140.hp1 HG00280.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.3539+58G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 28/31 | chr5 | 176590745 | ||||||
chr5:176590748
|
G | A | 3 | a0002c0001t0001g0140a0002c0001t0001g0142a0002c0001t0001g0151 | 3 | HG02809.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3539+61G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 28/31 | chr5 | 176590748 | ||||||
chr5:176591008
|
A | G | 1 | a0001c0005t0001g0311 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3540-202A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 28/31 | chr5 | 176591008 | ||||||
chr5:176591089
|
C | T | 92 | a0002c0001t0001g0001a0002c0001t0001g0005a0002c0001t0001g0006others(89): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.3540-121C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 28/31 | chr5 | 176591089 | ||||||
chr5:176591095
|
A | G | 1 | a0002c0001t0001g0158 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3540-115A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 28/31 | chr5 | 176591095 | ||||||
chr5:176591166
|
C | T | 1 | a0007c0031t0001g0317 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3540-44C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 28/31 | chr5 | 176591166 | ||||||
chr5:176591508
|
G | A | 1 | a0002c0001t0001g0034 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3734+24G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591508 | ||||||
chr5:176591539
|
C | CGGT | 2 | a0006c0014t0001g0003a0006c0014t0001g0045 | 3 | HG02622.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3734+66_3734+68dup others(3): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591539 | |||||
chr5:176591544
|
G | A | 242 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(239): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.3734+60G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591544 | ||||||
chr5:176591559
|
TTGGTGGT others(5): Show |
T | 1 | a0003c0002t0001g0197 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3734+81_3734+92del others(12): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591559 | |||||
chr5:176591569
|
T | A | 1 | a0003c0002t0001g0208 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3734+85T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591569 | ||||||
chr5:176591601
|
T | C | 1 | a0001c0003t0001g0161 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3734+117T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591601 | ||||||
chr5:176591618
|
A | G | 10 | a0001c0006t0001g0141a0001c0006t0001g0170a0004c0039t0001g0024others(7): Show | 11 | HG02622.hp1 HG02723.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.3734+134A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591618 | ||||||
chr5:176591618
|
ATGG | A | 52 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(49): Show | 59 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.3734+146_3734+148d others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591618 | |||||
chr5:176591682
|
G | A | 1 | a0001c0005t0001g0311 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3734+198G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591682 | ||||||
chr5:176591689
|
A | ATGATGAT others(1636): Show |
2 | a0013c0022t0001g0261a0013c0022t0001g0262 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3734+210_3734+211i others(1645): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGAT others(1636): Show |
1 | a0001c0006t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3734+210_3734+211i others(1645): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGAT others(1948): Show |
1 | a0001c0006t0001g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3734+210_3734+211i others(1957): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGAT others(1742): Show |
1 | a0004c0039t0001g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3734+210_3734+211i others(1751): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(2339): Show |
1 | a0001c0013t0001g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3734+225_3734+226i others(2348): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(1700): Show |
1 | a0001c0008t0001g0165 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3734+225_3734+226i others(1709): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(1806): Show |
4 | a0001c0008t0001g0166a0001c0008t0001g0178a0001c0013t0001g0002others(1): Show | 6 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.3734+225_3734+226i others(1815): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(1924): Show |
1 | a0001c0038t0001g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3734+225_3734+226i others(1933): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(46): Show |
3 | a0001c0004t0001g0289a0003c0002t0001g0228a0003c0002t0001g0231 | 3 | HG04199.hp2 NA19080.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3734+226_3734+278d others(55): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(129): Show |
1 | a0003c0002t0001g0229 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3734+279_3734+414d others(138): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(99): Show |
5 | a0001c0016t0001g0014a0001c0016t0001g0137a0004c0010t0001g0016others(2): Show | 8 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.3734+278_3734+279i others(108): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(182): Show |
62 | a0001c0025t0001g0216a0003c0002t0001g0020a0003c0002t0001g0164others(59): Show | 63 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.3734+278_3734+279i others(191): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(205): Show |
2 | a0003c0002t0001g0187a0003c0002t0001g0234 | 2 | HG02056.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3734+278_3734+279i others(214): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(288): Show |
2 | a0003c0002t0001g0206a0003c0002t0001g0224 | 2 | NA19001.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.3734+278_3734+279i others(297): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(341): Show |
15 | a0003c0002t0001g0019a0003c0002t0001g0072a0003c0002t0001g0106others(12): Show | 16 | HG01934.hp1 HG01934.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.3734+278_3734+279i others(350): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(447): Show |
1 | a0003c0002t0001g0217 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3734+278_3734+279i others(456): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(500): Show |
1 | a0003c0002t0001g0226 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3734+278_3734+279i others(509): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(1469): Show |
1 | a0001c0017t0001g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3734+228_3734+229i others(1478): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
A | ATGATGGT others(1519): Show |
2 | a0001c0017t0001g0134a0001c0017t0001g0135 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3734+228_3734+229i others(1528): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591689
|
ATGATGGT others(129): Show |
A | 3 | a0001c0005t0001g0013a0001c0005t0001g0173a0001c0005t0001g0296 | 4 | HG03139.hp2 HG03453.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.3734+279_3734+414d others(2): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591689 | |||||
chr5:176591707
|
G | GTGGTGAT others(203): Show |
2 | a0001c0008t0001g0176a0001c0008t0001g0177 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3734+225_3734+226i others(212): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591707 | |||||
chr5:176591710
|
T | G | 2 | a0001c0008t0001g0176a0001c0008t0001g0177 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3734+226T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591710 | ||||||
chr5:176591710
|
T | TTGTTGAG others(176): Show |
2 | a0001c0004t0001g0169a0014c0020t0001g0180 | 2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3734+228_3734+229i others(185): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591710 | |||||
chr5:176591713
|
G | T | 2 | a0001c0004t0001g0169a0014c0020t0001g0180 | 2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3734+229G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591713 | ||||||
chr5:176591735
|
T | G | 1 | a0022c0054t0001g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3734+251T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591735 | ||||||
chr5:176591754
|
A | ATGATGGT others(13): Show |
1 | a0001c0003t0001g0101 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3734+278_3734+279i others(22): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591754 | |||||
chr5:176591754
|
A | ATGATGGT others(914): Show |
1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3734+278_3734+279i others(923): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591754 | |||||
chr5:176591761
|
T | TGTTGGTG others(4): Show |
134 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(131): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.3734+278_3734+279i others(13): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591761 | |||||
chr5:176591762
|
G | GTTGGTGT others(19): Show |
1 | a0002c0001t0001g0123 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3734+278_3734+279i others(28): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591762 | ||||||
chr5:176591763
|
A | G | 135 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(132): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.3734+279A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591763 | ||||||
chr5:176591763
|
A | T | 15 | a0001c0003t0001g0047a0001c0003t0001g0304a0001c0003t0001g0307others(12): Show | 17 | HG00642.hp1 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.3734+279A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591763 | ||||||
chr5:176591765
|
G | GGTGTTGA others(1238): Show |
1 | a0022c0054t0001g0175 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3734+281_3734+282i others(1247): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591765 | ||||||
chr5:176591765
|
G | GGTGTTGA others(122): Show |
2 | a0010c0018t0001g0004a0010c0018t0001g0057 | 3 | HG00642.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.3734+281_3734+282i others(131): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591765 | ||||||
chr5:176591765
|
G | GGTGTTGA others(228): Show |
1 | a0002c0001t0001g0115 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3734+281_3734+282i others(237): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591765 | ||||||
chr5:176591765
|
G | GGTGTTGA others(281): Show |
2 | a0002c0001t0001g0129a0002c0001t0001g0130 | 2 | HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.3734+281_3734+282i others(290): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591765 | ||||||
chr5:176591765
|
G | GGTGTTGA others(334): Show |
3 | a0002c0001t0001g0116a0006c0014t0001g0003a0006c0014t0001g0045 | 4 | HG02622.hp1 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3734+281_3734+282i others(343): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591765 | ||||||
chr5:176591765
|
G | GGTGTTGA others(864): Show |
2 | a0007c0031t0001g0316a0007c0031t0001g0317 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3734+281_3734+282i others(873): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591765 | ||||||
chr5:176591765
|
G | GGTGTTGA others(2083): Show |
1 | a0001c0003t0001g0047 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3734+281_3734+282i others(2092): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591765 | ||||||
chr5:176591765
|
G | GGTGTTGA others(1921): Show |
1 | a0001c0003t0001g0304 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3734+281_3734+282i others(1930): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591765 | ||||||
chr5:176591765
|
G | GGTGTTGA others(1766): Show |
1 | a0001c0003t0001g0307 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3734+281_3734+282i others(1775): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591765 | ||||||
chr5:176591766
|
A | ATGATGGT others(1159): Show |
1 | a0002c0001t0001g0123 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3734+285_3734+286i others(1168): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591766 | |||||
chr5:176591766
|
A | G | 17 | a0001c0003t0001g0047a0001c0003t0001g0101a0001c0003t0001g0259others(14): Show | 19 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.3734+282A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591766 | ||||||
chr5:176591769
|
A | G | 136 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(133): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.3734+285A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591769 | ||||||
chr5:176591770
|
C | T | 152 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(149): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.3734+286C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591770 | ||||||
chr5:176591772
|
A | G | 16 | a0001c0003t0001g0047a0001c0003t0001g0304a0001c0003t0001g0307others(13): Show | 18 | HG00642.hp1 HG00741.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.3734+288A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591772 | ||||||
chr5:176591772
|
ATGG | A | 21 | a0001c0006t0001g0141a0001c0006t0001g0170a0001c0008t0001g0165others(18): Show | 23 | HG00408.hp2 HG01069.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.3734+306_3734+308d others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591772 | |||||
chr5:176591775
|
G | A | 16 | a0001c0003t0001g0047a0001c0003t0001g0304a0001c0003t0001g0307others(13): Show | 18 | HG00642.hp1 HG00741.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.3734+291G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591775 | ||||||
chr5:176591775
|
G | GTGATGGT others(2272): Show |
1 | a0001c0003t0001g0101 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3734+293_3734+294i others(2281): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(5): Show |
9 | a0001c0003t0001g0162a0002c0001t0001g0056a0002c0001t0001g0113others(6): Show | 9 | HG01167.hp2 HG02055.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.3734+292_3734+293i others(14): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1301): Show |
1 | a0002c0023t0001g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3734+292_3734+293i others(1310): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1118): Show |
1 | a0001c0003t0001g0160 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3734+292_3734+293i others(1127): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(588): Show |
1 | a0001c0003t0001g0012 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.3734+292_3734+293i others(597): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(959): Show |
1 | a0001c0005t0001g0200 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3734+292_3734+293i others(968): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(694): Show |
1 | a0002c0001t0001g0055 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3734+292_3734+293i others(703): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2072): Show |
1 | a0001c0003t0003g0105 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3734+292_3734+293i others(2081): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(747): Show |
1 | a0002c0001t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3734+292_3734+293i others(756): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2072): Show |
1 | a0001c0003t0001g0023 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3734+292_3734+293i others(2081): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2072): Show |
1 | a0001c0003t0001g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3734+292_3734+293i others(2081): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2072): Show |
3 | a0001c0003t0001g0305a0001c0003t0001g0306a0001c0003t0001g0308 | 3 | HG00642.hp2 HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3734+292_3734+293i others(2081): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(853): Show |
1 | a0002c0001t0001g0082 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3734+292_3734+293i others(862): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2125): Show |
1 | a0001c0003t0001g0102 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3734+292_3734+293i others(2134): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2072): Show |
1 | a0001c0003t0001g0039 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3734+292_3734+293i others(2081): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2125): Show |
1 | a0001c0003t0001g0161 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3734+292_3734+293i others(2134): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2125): Show |
1 | a0001c0003t0001g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3734+292_3734+293i others(2134): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2125): Show |
7 | a0001c0003t0001g0021a0001c0003t0001g0061a0001c0003t0001g0107others(4): Show | 8 | HG00735.hp1 HG00738.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.3734+292_3734+293i others(2134): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1224): Show |
2 | a0005c0007t0001g0138a0005c0007t0001g0139 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3734+292_3734+293i others(1233): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1224): Show |
5 | a0001c0005t0001g0018a0005c0007t0001g0009a0005c0007t0001g0062others(2): Show | 7 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.3734+292_3734+293i others(1233): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1224): Show |
1 | a0001c0005t0001g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3734+292_3734+293i others(1233): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(959): Show |
3 | a0002c0001t0001g0149a0011c0028t0001g0145a0011c0028t0001g0302 | 3 | HG01361.hp2 HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.3734+292_3734+293i others(968): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1648): Show |
1 | a0001c0003t0001g0318 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3734+292_3734+293i others(1657): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1012): Show |
3 | a0002c0001t0001g0015a0002c0001t0001g0125a0002c0001t0001g0148 | 4 | HG00735.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.3734+292_3734+293i others(1021): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1065): Show |
1 | a0004c0055t0001g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3734+292_3734+293i others(1074): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1118): Show |
7 | a0001c0003t0001g0301a0002c0001t0001g0025a0002c0001t0001g0028others(4): Show | 7 | HG01361.hp1 HG02622.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3734+292_3734+293i others(1127): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1171): Show |
18 | a0002c0001t0001g0006a0002c0001t0001g0008a0002c0001t0001g0060others(15): Show | 20 | HG00438.hp1 HG00438.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.3734+292_3734+293i others(1180): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2019): Show |
1 | a0001c0003t0001g0104 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3734+292_3734+293i others(2028): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1224): Show |
8 | a0002c0001t0001g0007a0002c0001t0001g0038a0002c0001t0001g0063others(5): Show | 9 | HG01516.hp1 HG02040.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.3734+292_3734+293i others(1233): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1277): Show |
26 | a0002c0001t0001g0001a0002c0001t0001g0005a0002c0001t0001g0049others(23): Show | 30 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(27): Show |
intron_variant | MODIFIER | c.3734+292_3734+293i others(1286): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1754): Show |
2 | a0001c0041t0001g0264a0006c0019t0001g0043 | 2 | HG01884.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.3734+292_3734+293i others(1763): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1330): Show |
8 | a0002c0001t0001g0026a0002c0001t0001g0034a0002c0001t0001g0052others(5): Show | 8 | HG00741.hp2 HG01175.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3734+292_3734+293i others(1339): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1383): Show |
1 | a0012c0021t0001g0314 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3734+292_3734+293i others(1392): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2019): Show |
1 | a0001c0003t0001g0098 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3734+292_3734+293i others(2028): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1913): Show |
1 | a0001c0003t0001g0103 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3734+292_3734+293i others(1922): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1436): Show |
1 | a0002c0001t0001g0069 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.3734+292_3734+293i others(1445): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2125): Show |
1 | a0001c0003t0001g0048 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3734+292_3734+293i others(2134): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1489): Show |
2 | a0002c0001t0001g0081a0002c0001t0001g0108 | 2 | HG01256.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.3734+292_3734+293i others(1498): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2125): Show |
1 | a0001c0003t0001g0099 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3734+292_3734+293i others(2134): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2125): Show |
1 | a0001c0003t0001g0010 | 2 | HG01074.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3734+292_3734+293i others(2134): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1542): Show |
1 | a0002c0030t0001g0284 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3734+292_3734+293i others(1551): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2178): Show |
1 | a0001c0003t0001g0122 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3734+292_3734+293i others(2187): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1595): Show |
1 | a0023c0034t0001g0251 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3734+292_3734+293i others(1604): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(2284): Show |
1 | a0001c0003t0001g0100 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3734+292_3734+293i others(2293): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(3238): Show |
1 | a0006c0019t0001g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3734+292_3734+293i others(3247): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591775
|
G | GTTGTGAT others(1816): Show |
1 | a0002c0001t0001g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3734+292_3734+293i others(1825): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591775 | |||||
chr5:176591784
|
G | A | 152 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(149): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.3734+300G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591784 | ||||||
chr5:176591787
|
G | A | 152 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(149): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.3734+303G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591787 | ||||||
chr5:176591787
|
G | GTGGTGTT others(46): Show |
4 | a0004c0009t0001g0146a0004c0009t0001g0147a0004c0009t0001g0312others(1): Show | 4 | HG01891.hp1 HG02559.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3734+415_3734+467d others(55): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591787 | |||||
chr5:176591787
|
G | GTGGTGTT others(205): Show |
1 | a0001c0004t0001g0265 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3734+467_3734+468i others(214): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591787 | |||||
chr5:176591787
|
G | GTGGTGTT others(523): Show |
1 | a0001c0004t0001g0290 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3734+467_3734+468i others(532): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591787 | |||||
chr5:176591825
|
G | GTGATGGT others(26): Show |
5 | a0001c0006t0001g0141a0001c0006t0001g0170a0004c0039t0001g0024others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3734+361_3734+362i others(35): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591825 | |||||
chr5:176591826
|
T | TGAC | 3 | a0007c0031t0001g0316a0007c0031t0001g0317a0022c0054t0001g0175 | 3 | HG02717.hp2 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3734+344_3734+345i others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591826 | |||||
chr5:176591826
|
T | TGATGGTG others(738): Show |
2 | a0007c0027t0001g0035a0007c0027t0001g0036 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3734+467_3734+468i others(747): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591826 | |||||
chr5:176591849
|
G | A | 1 | a0001c0004t0001g0278 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3734+365G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591849 | ||||||
chr5:176591871
|
T | G | 7 | a0001c0008t0001g0165a0001c0008t0001g0166a0001c0008t0001g0178others(4): Show | 9 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.3734+387T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591871 | ||||||
chr5:176591878
|
G | A | 7 | a0001c0008t0001g0165a0001c0008t0001g0166a0001c0008t0001g0178others(4): Show | 9 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.3734+394G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591878 | ||||||
chr5:176591879
|
T | TGAC | 8 | a0001c0005t0001g0311a0001c0008t0001g0165a0001c0008t0001g0166others(5): Show | 10 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.3734+397_3734+398i others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591879 | |||||
chr5:176591890
|
A | ATGATGGT others(844): Show |
1 | a0007c0050t0001g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3734+467_3734+468i others(853): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591890 | |||||
chr5:176591890
|
A | G | 2 | a0007c0031t0001g0316a0007c0031t0001g0317 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3734+406A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591890 | ||||||
chr5:176591893
|
A | ATGACGAT others(11): Show |
5 | a0001c0006t0001g0141a0001c0006t0001g0170a0004c0039t0001g0024others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3734+411_3734+412i others(20): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591893 | |||||
chr5:176591893
|
A | ATGGTGTT others(797): Show |
3 | a0001c0017t0001g0134a0001c0017t0001g0135a0001c0017t0001g0144 | 3 | HG02976.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3734+467_3734+468i others(806): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591893 | |||||
chr5:176591896
|
GTGTTGGT others(43): Show |
G | 2 | a0001c0006t0001g0111a0001c0006t0001g0117 | 2 | HG01928.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.3734+415_3734+464d others(52): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591896 | |||||
chr5:176591903
|
T | TGTTGAGG others(1106): Show |
1 | a0002c0001t0001g0132 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3734+467_3734+468i others(1115): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591903 | |||||
chr5:176591923
|
T | TTGTGATG others(1266): Show |
1 | a0002c0001t0001g0113 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3734+467_3734+468i others(1275): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591923 | |||||
chr5:176591936
|
G | GGTGGTGA others(1223): Show |
1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3734+467_3734+468i others(1232): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591936 | |||||
chr5:176591943
|
A | ATGATGGT others(670): Show |
1 | a0001c0003t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3734+467_3734+468i others(679): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591943 | |||||
chr5:176591949
|
G | A | 2 | a0001c0006t0001g0111a0001c0006t0001g0117 | 2 | HG01928.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.3734+465G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591949 | ||||||
chr5:176591951
|
G | GTTGGTGT others(19): Show |
1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3734+467_3734+468i others(28): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591951 | ||||||
chr5:176591951
|
G | GTTGGTGT others(549): Show |
1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3734+467_3734+468i others(558): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591951 | ||||||
chr5:176591952
|
A | G | 3 | a0001c0003t0001g0162a0002c0026t0001g0293a0012c0021t0001g0037 | 3 | HG04184.hp1 NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+468A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591952 | ||||||
chr5:176591952
|
A | T | 1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3734+468A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591952 | ||||||
chr5:176591955
|
A | G | 1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3734+471A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591955 | ||||||
chr5:176591956
|
T | C | 2 | a0001c0006t0001g0111a0001c0006t0001g0117 | 2 | HG01928.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.3734+472T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591956 | ||||||
chr5:176591957
|
G | GTTGAGGT others(758): Show |
1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3734+473_3734+474i others(767): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591957 | ||||||
chr5:176591958
|
A | G | 3 | a0002c0001t0001g0056a0002c0026t0001g0293a0012c0021t0001g0037 | 3 | NA18981.hp2 NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+474A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591958 | ||||||
chr5:176591959
|
C | CGAT | 246 | a0001c0004t0001g0022a0001c0004t0001g0040a0001c0004t0001g0169others(243): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.3734+476_3734+477i others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591959 | |||||
chr5:176591959
|
C | CGGT | 8 | a0001c0008t0001g0165a0001c0008t0001g0166a0001c0008t0001g0178others(5): Show | 10 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.3734+492_3734+494d others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176591959 | |||||
chr5:176591959
|
C | G | 1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3734+475C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591959 | ||||||
chr5:176591959
|
C | T | 5 | a0001c0003t0001g0162a0001c0006t0001g0111a0001c0006t0001g0117others(2): Show | 5 | HG01928.hp1 HG04184.hp1 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.3734+475C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591959 | ||||||
chr5:176591961
|
G | A | 57 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(54): Show | 64 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.3734+477G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591961 | ||||||
chr5:176591964
|
G | T | 1 | a0001c0003t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3734+480G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591964 | ||||||
chr5:176591970
|
G | A | 2 | a0002c0026t0001g0293a0012c0021t0001g0037 | 2 | NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+486G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591970 | ||||||
chr5:176591973
|
G | A | 3 | a0001c0003t0001g0162a0002c0026t0001g0293a0012c0021t0001g0037 | 3 | HG04184.hp1 NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+489G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591973 | ||||||
chr5:176591976
|
G | T | 1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3734+492G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591976 | ||||||
chr5:176591979
|
T | A | 1 | a0001c0003t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3734+495T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591979 | ||||||
chr5:176591979
|
T | G | 2 | a0001c0003t0001g0259a0001c0005t0001g0046 | 2 | NA20805.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3734+495T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591979 | ||||||
chr5:176591982
|
G | T | 1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3734+498G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591982 | ||||||
chr5:176591985
|
T | G | 1 | a0001c0003t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3734+501T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591985 | ||||||
chr5:176591988
|
A | G | 2 | a0002c0001t0001g0068a0002c0001t0001g0083 | 2 | NA18939.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.3734+504A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176591988 | ||||||
chr5:176592005
|
G | A | 1 | a0001c0003t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3734+521G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592005 | ||||||
chr5:176592007
|
A | G | 3 | a0001c0003t0001g0162a0002c0026t0001g0293a0012c0021t0001g0037 | 3 | HG04184.hp1 NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+523A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592007 | ||||||
chr5:176592008
|
G | A | 2 | a0002c0026t0001g0293a0012c0021t0001g0037 | 2 | NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+524G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592008 | ||||||
chr5:176592011
|
G | T | 1 | a0001c0003t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3734+527G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592011 | ||||||
chr5:176592018
|
G | A | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3734+534G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592018 | ||||||
chr5:176592026
|
G | T | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3734+542G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592026 | ||||||
chr5:176592027
|
G | T | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3734+543G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592027 | ||||||
chr5:176592031
|
C | T | 1 | a0001c0003t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3734+547C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592031 | ||||||
chr5:176592032
|
A | G | 2 | a0001c0003t0001g0162a0002c0001t0001g0056 | 2 | HG04184.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.3734+548A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592032 | ||||||
chr5:176592036
|
G | T | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3734+552G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592036 | ||||||
chr5:176592045
|
G | A | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3734+561G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592045 | ||||||
chr5:176592048
|
G | A | 2 | a0001c0003t0001g0162a0012c0021t0001g0037 | 2 | HG04184.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+564G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592048 | ||||||
chr5:176592049
|
T | G | 1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3734+565T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592049 | ||||||
chr5:176592050
|
C | G | 3 | a0001c0003t0001g0162a0002c0026t0001g0293a0012c0021t0001g0037 | 3 | HG04184.hp1 NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+566C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592050 | ||||||
chr5:176592050
|
C | T | 1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3734+566C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592050 | ||||||
chr5:176592056
|
G | T | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3734+572G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592056 | ||||||
chr5:176592058
|
T | A | 2 | a0001c0003t0001g0162a0012c0021t0001g0037 | 2 | HG04184.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+574T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592058 | ||||||
chr5:176592059
|
C | G | 3 | a0001c0003t0001g0162a0002c0026t0001g0293a0012c0021t0001g0037 | 3 | HG04184.hp1 NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+575C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592059 | ||||||
chr5:176592060
|
A | G | 2 | a0001c0003t0001g0162a0012c0021t0001g0037 | 2 | HG04184.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+576A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592060 | ||||||
chr5:176592063
|
G | A | 2 | a0001c0003t0001g0162a0012c0021t0001g0037 | 2 | HG04184.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+579G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592063 | ||||||
chr5:176592065
|
A | G | 3 | a0001c0003t0001g0162a0002c0026t0001g0293a0012c0021t0001g0037 | 3 | HG04184.hp1 NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+581A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592065 | ||||||
chr5:176592066
|
G | A | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3734+582G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592066 | ||||||
chr5:176592069
|
G | A | 2 | a0001c0003t0001g0162a0012c0021t0001g0037 | 2 | HG04184.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+585G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592069 | ||||||
chr5:176592073
|
C | T | 3 | a0001c0003t0001g0162a0002c0026t0001g0293a0012c0021t0001g0037 | 3 | HG04184.hp1 NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+589C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592073 | ||||||
chr5:176592074
|
A | G | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3734+590A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592074 | ||||||
chr5:176592074
|
A | T | 2 | a0001c0003t0001g0162a0012c0021t0001g0037 | 2 | HG04184.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+590A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592074 | ||||||
chr5:176592075
|
G | A | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3734+591G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592075 | ||||||
chr5:176592077
|
T | G | 3 | a0001c0003t0001g0162a0002c0026t0001g0293a0012c0021t0001g0037 | 3 | HG04184.hp1 NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+593T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592077 | ||||||
chr5:176592079
|
TCGTGGTG others(6): Show |
T | 1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3734+596_3734+608d others(15): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592079 | ||||||
chr5:176592080
|
C | G | 3 | a0001c0003t0001g0162a0002c0026t0001g0293a0012c0021t0001g0037 | 3 | HG04184.hp1 NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+596C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592080 | ||||||
chr5:176592080
|
C | T | 58 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(55): Show | 67 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.3734+596C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592080 | ||||||
chr5:176592081
|
G | A | 1 | a0003c0002t0001g0212 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3734+597G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592081 | ||||||
chr5:176592084
|
G | A | 2 | a0001c0003t0001g0162a0012c0021t0001g0037 | 2 | HG04184.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+600G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592084 | ||||||
chr5:176592084
|
G | T | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3734+600G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592084 | ||||||
chr5:176592084
|
GTGGTGGT others(5): Show |
G | 52 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(49): Show | 59 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.3734+618_3735-610d others(14): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592084 | |||||
chr5:176592091
|
T | A | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3734+607T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592091 | ||||||
chr5:176592093
|
G | A | 2 | a0001c0003t0001g0162a0012c0021t0001g0037 | 2 | HG04184.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+609G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592093 | ||||||
chr5:176592096
|
A | ATGGTGGT others(501): Show |
1 | a0001c0038t0001g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3735-530_3735-529i others(510): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592096 | |||||
chr5:176592096
|
A | ATGGTGGT others(516): Show |
6 | a0001c0008t0001g0165a0001c0008t0001g0166a0001c0008t0001g0178others(3): Show | 8 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.3735-530_3735-529i others(525): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592096 | |||||
chr5:176592096
|
A | G | 1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3734+612A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592096 | ||||||
chr5:176592103
|
T | A | 2 | a0001c0003t0001g0162a0012c0021t0001g0037 | 2 | HG04184.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3734+619T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592103 | ||||||
chr5:176592104
|
G | T | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3735-619G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592104 | ||||||
chr5:176592119
|
A | G | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3735-604A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592119 | ||||||
chr5:176592119
|
A | T | 2 | a0001c0003t0001g0162a0012c0021t0001g0037 | 2 | HG04184.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3735-604A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592119 | ||||||
chr5:176592120
|
GTGATGGT others(73): Show |
G | 1 | a0001c0004t0001g0285 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3735-523_3735-444d others(82): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592120 | |||||
chr5:176592129
|
A | T | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3735-594A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592129 | ||||||
chr5:176592135
|
G | T | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3735-588G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592135 | ||||||
chr5:176592138
|
ATGATGG | A | 94 | a0002c0001t0001g0001a0002c0001t0001g0005a0002c0001t0001g0006others(91): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.3735-579_3735-574d others(8): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592138 | |||||
chr5:176592147
|
A | T | 1 | a0001c0003t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3735-576A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592147 | ||||||
chr5:176592149
|
G | GGTGTTGA others(303): Show |
1 | a0001c0003t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3735-574_3735-573i others(312): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592149 | ||||||
chr5:176592150
|
A | G | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-573A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592150 | ||||||
chr5:176592154
|
C | T | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-569C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592154 | ||||||
chr5:176592155
|
A | G | 3 | a0001c0003t0001g0162a0002c0026t0001g0293a0012c0021t0001g0037 | 3 | HG04184.hp1 NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3735-568A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592155 | ||||||
chr5:176592156
|
A | G | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-567A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592156 | ||||||
chr5:176592159
|
A | G | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3735-564A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592159 | ||||||
chr5:176592162
|
A | G | 3 | a0001c0003t0001g0162a0002c0026t0001g0293a0012c0021t0001g0037 | 3 | HG04184.hp1 NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3735-561A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592162 | ||||||
chr5:176592168
|
G | A | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-555G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592168 | ||||||
chr5:176592171
|
G | A | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-552G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592171 | ||||||
chr5:176592191
|
A | ATGGTGGT others(111): Show |
1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3735-530_3735-529i others(120): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592191 | |||||
chr5:176592199
|
G | A | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3735-524G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592199 | ||||||
chr5:176592199
|
G | T | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3735-524G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592199 | ||||||
chr5:176592200
|
C | G | 3 | a0001c0003t0001g0162a0002c0026t0001g0293a0012c0021t0001g0037 | 3 | HG04184.hp1 NA19009.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3735-523C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592200 | ||||||
chr5:176592224
|
GTGATGAT others(4): Show |
G | 1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3735-498_3735-488d others(13): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592224 | ||||||
chr5:176592227
|
A | T | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-496A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592227 | ||||||
chr5:176592230
|
A | G | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-493A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592230 | ||||||
chr5:176592233
|
A | T | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-490A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592233 | ||||||
chr5:176592234
|
C | T | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-489C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592234 | ||||||
chr5:176592235
|
A | G | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-488A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592235 | ||||||
chr5:176592239
|
A | G | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-484A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592239 | ||||||
chr5:176592242
|
A | G | 1 | a0002c0001t0001g0090 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3735-481A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592242 | ||||||
chr5:176592242
|
ATGG | A | 5 | a0001c0006t0001g0141a0001c0006t0001g0170a0004c0039t0001g0024others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3735-469_3735-467d others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592242 | |||||
chr5:176592245
|
G | A | 1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3735-478G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592245 | ||||||
chr5:176592248
|
G | A | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-475G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592248 | ||||||
chr5:176592253
|
G | T | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3735-470G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592253 | ||||||
chr5:176592257
|
T | A | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-466T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592257 | ||||||
chr5:176592264
|
T | G | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-459T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592264 | ||||||
chr5:176592266
|
A | T | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-457A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592266 | ||||||
chr5:176592271
|
ATGATGGT others(8): Show |
A | 1 | a0001c0004t0001g0282 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3735-425_3735-411d others(17): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592271 | |||||
chr5:176592278
|
T | TGTTGGTG others(4): Show |
2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-444_3735-443i others(13): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592278 | |||||
chr5:176592283
|
A | G | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3735-440A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592283 | ||||||
chr5:176592284
|
T | G | 1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3735-439T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592284 | ||||||
chr5:176592289
|
A | T | 1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3735-434A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592289 | ||||||
chr5:176592289
|
ATGGTGGT others(5): Show |
A | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3735-431_3735-420d others(14): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592289 | |||||
chr5:176592294
|
G | T | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-429G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592294 | ||||||
chr5:176592298
|
A | G | 1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3735-425A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592298 | ||||||
chr5:176592298
|
ATGG | A | 11 | a0001c0005t0001g0311a0001c0017t0001g0134a0001c0017t0001g0135others(8): Show | 11 | HG02055.hp1 HG02486.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.3735-422_3735-420d others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592298 | |||||
chr5:176592301
|
G | A | 147 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(144): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.3735-422G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592301 | ||||||
chr5:176592307
|
G | A | 13 | a0001c0005t0001g0311a0001c0017t0001g0134a0001c0017t0001g0135others(10): Show | 13 | HG02055.hp1 HG02486.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.3735-416G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592307 | ||||||
chr5:176592313
|
G | A | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-410G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592313 | ||||||
chr5:176592316
|
G | A | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-407G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592316 | ||||||
chr5:176592322
|
T | G | 1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3735-401T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592322 | ||||||
chr5:176592328
|
T | G | 1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3735-395T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592328 | ||||||
chr5:176592345
|
A | G | 1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3735-378A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592345 | ||||||
chr5:176592355
|
TAGTGATG others(28): Show |
T | 1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3735-367_3735-333d others(37): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592355 | ||||||
chr5:176592356
|
A | G | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-367A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592356 | ||||||
chr5:176592360
|
A | G | 2 | a0002c0001t0001g0056a0004c0039t0001g0024 | 2 | HG02723.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.3735-363A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592360 | ||||||
chr5:176592363
|
G | A | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-360G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592363 | ||||||
chr5:176592366
|
A | G | 3 | a0001c0003t0001g0162a0002c0001t0001g0056a0002c0026t0001g0293 | 3 | HG04184.hp1 NA18981.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-357A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592366 | ||||||
chr5:176592367
|
T | TGTTGGTG others(4): Show |
2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-355_3735-354i others(13): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592367 | |||||
chr5:176592372
|
G | A | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-351G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592372 | ||||||
chr5:176592375
|
G | A | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3735-348G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592375 | ||||||
chr5:176592383
|
TATG | T | 8 | a0001c0005t0001g0311a0003c0002t0001g0156a0007c0027t0001g0035others(5): Show | 8 | HG02055.hp1 HG02148.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.3735-330_3735-328d others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592383 | |||||
chr5:176592384
|
A | G | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-339A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592384 | ||||||
chr5:176592390
|
A | G | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-333A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592390 | ||||||
chr5:176592391
|
T | G | 1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3735-332T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592391 | ||||||
chr5:176592402
|
G | A | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-321G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592402 | ||||||
chr5:176592402
|
G | T | 4 | a0003c0002t0001g0202a0003c0002t0001g0203a0003c0002t0001g0218others(1): Show | 4 | NA18951.hp2 NA18952.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.3735-321G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592402 | ||||||
chr5:176592405
|
G | T | 1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3735-318G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592405 | ||||||
chr5:176592406
|
T | G | 1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3735-317T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592406 | ||||||
chr5:176592428
|
A | G | 1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3735-295A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592428 | ||||||
chr5:176592428
|
ATGG | A | 48 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(45): Show | 55 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.3735-289_3735-287d others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592428 | |||||
chr5:176592431
|
G | T | 1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3735-292G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592431 | ||||||
chr5:176592433
|
G | T | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-290G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592433 | ||||||
chr5:176592437
|
A | G | 1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3735-286A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592437 | ||||||
chr5:176592439
|
G | GGTGATGG others(1052): Show |
1 | a0001c0003t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3735-284_3735-283i others(1061): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592439 | ||||||
chr5:176592440
|
A | G | 2 | a0001c0003t0001g0162a0002c0026t0001g0293 | 2 | HG04184.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3735-283A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592440 | ||||||
chr5:176592442
|
G | GATGGTGG others(1150): Show |
1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3735-281_3735-280i others(1159): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592442 | ||||||
chr5:176592442
|
G | T | 1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3735-281G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592442 | ||||||
chr5:176592451
|
C | G | 1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3735-272C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592451 | ||||||
chr5:176592451
|
C | T | 2 | a0001c0003t0001g0259a0002c0026t0001g0293 | 2 | NA19009.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3735-272C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592451 | ||||||
chr5:176592453
|
G | C | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3735-270G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592453 | ||||||
chr5:176592454
|
T | C | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3735-269T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592454 | ||||||
chr5:176592470
|
G | A | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3735-253G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592470 | ||||||
chr5:176592474
|
T | G | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3735-249T>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592474 | ||||||
chr5:176592477
|
A | G | 1 | a0001c0003t0001g0162 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3735-246A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592477 | ||||||
chr5:176592490
|
G | A | 1 | a0001c0004t0001g0289 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3735-233G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592490 | ||||||
chr5:176592497
|
G | T | 1 | a0002c0001t0001g0056 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3735-226G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592497 | ||||||
chr5:176592507
|
T | C | 102 | a0001c0005t0001g0311a0002c0001t0001g0001a0002c0001t0001g0005others(99): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.3735-216T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592507 | ||||||
chr5:176592517
|
A | AGTG | 101 | a0001c0005t0001g0311a0002c0001t0001g0001a0002c0001t0001g0005others(98): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.3735-193_3735-191d others(5): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr5 | 176592517 | |||||
chr5:176592528
|
T | A | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3735-195T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592528 | ||||||
chr5:176592557
|
T | A | 1 | a0002c0026t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3735-166T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 30/31 | chr5 | 176592557 | ||||||
chr5:176592856
|
G | A | 1 | a0002c0001t0001g0093 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3792+76G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176592856 | ||||||
chr5:176592870
|
A | G | 1 | a0001c0005t0001g0311 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3792+90A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176592870 | ||||||
chr5:176592969
|
T | A | 12 | a0001c0005t0001g0013a0001c0005t0001g0018a0001c0005t0001g0046others(9): Show | 15 | HG00140.hp1 HG00280.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.3792+189T>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176592969 | ||||||
chr5:176593025
|
C | T | 1 | a0001c0003t0001g0161 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3792+245C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176593025 | ||||||
chr5:176593158
|
C | G | 102 | a0001c0005t0001g0311a0002c0001t0001g0001a0002c0001t0001g0005others(99): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.3792+378C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176593158 | ||||||
chr5:176593202
|
T | C | 95 | a0002c0001t0001g0001a0002c0001t0001g0005a0002c0001t0001g0006others(92): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.3792+422T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176593202 | ||||||
chr5:176593240
|
A | AGTTG | 11 | a0001c0004t0001g0169a0001c0008t0001g0165a0001c0008t0001g0166others(8): Show | 13 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.3792+461_3792+462i others(6): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr5 | 176593240 | |||||
chr5:176593242
|
G | A | 11 | a0001c0004t0001g0169a0001c0008t0001g0165a0001c0008t0001g0166others(8): Show | 13 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.3792+462G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176593242 | ||||||
chr5:176593266
|
T | C | 1 | a0001c0004t0001g0272 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3792+486T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176593266 | ||||||
chr5:176593280
|
C | T | 1 | a0004c0039t0001g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3792+500C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176593280 | ||||||
chr5:176593311
|
G | A | 1 | a0003c0002t0001g0240 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3792+531G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176593311 | ||||||
chr5:176593437
|
CA | C | 3 | a0004c0010t0001g0016a0004c0010t0001g0017a0004c0010t0001g0032 | 5 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.3792+658delA | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176593437 | ||||||
chr5:176593448
|
A | T | 2 | a0002c0001t0001g0060a0002c0023t0001g0042 | 2 | HG00438.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.3792+668A>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176593448 | ||||||
chr5:176593611
|
G | C | 1 | a0002c0001t0001g0132 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3792+831G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176593611 | ||||||
chr5:176593627
|
C | G | 1 | a0012c0021t0001g0037 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3792+847C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176593627 | ||||||
chr5:176593746
|
C | T | 3 | a0001c0041t0001g0264a0006c0019t0001g0043a0006c0019t0001g0044 | 3 | HG01884.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3792+966C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176593746 | ||||||
chr5:176593762
|
A | G | 1 | a0001c0005t0001g0018 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3792+982A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176593762 | ||||||
chr5:176593837
|
C | T | 53 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(50): Show | 60 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.3792+1057C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176593837 | ||||||
chr5:176594040
|
G | T | 95 | a0002c0001t0001g0001a0002c0001t0001g0005a0002c0001t0001g0006others(92): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.3792+1260G>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176594040 | ||||||
chr5:176594058
|
C | T | 11 | a0001c0004t0001g0169a0001c0008t0001g0165a0001c0008t0001g0166others(8): Show | 13 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.3792+1278C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176594058 | ||||||
chr5:176594271
|
G | A | 1 | a0001c0003t0001g0310 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3793-1261G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176594271 | ||||||
chr5:176594418
|
G | A | 6 | a0002c0001t0001g0005a0002c0001t0001g0064a0002c0001t0001g0077others(3): Show | 7 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.3793-1114G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176594418 | ||||||
chr5:176594581
|
G | A | 1 | a0002c0001t0001g0158 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3793-951G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176594581 | ||||||
chr5:176594730
|
A | G | 2 | a0003c0002t0001g0192a0003c0002t0001g0247 | 2 | NA18945.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.3793-802A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176594730 | ||||||
chr5:176594840
|
G | GGT | 11 | a0001c0005t0001g0311a0002c0001t0001g0049a0002c0001t0001g0050others(8): Show | 11 | HG01243.hp1 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3793-678_3793-677d others(4): Show |
CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr5 | 176594840 | |||||
chr5:176594858
|
C | T | 1 | a0001c0004t0001g0295 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3793-674C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176594858 | ||||||
chr5:176594872
|
C | T | 11 | a0001c0004t0001g0169a0001c0008t0001g0165a0001c0008t0001g0166others(8): Show | 13 | HG01069.hp2 HG01070.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.3793-660C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176594872 | ||||||
chr5:176594936
|
G | C | 1 | a0001c0003t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3793-596G>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176594936 | ||||||
chr5:176594955
|
C | T | 78 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(75): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.3793-577C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176594955 | ||||||
chr5:176594980
|
A | G | 50 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(47): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.3793-552A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176594980 | ||||||
chr5:176595140
|
T | C | 3 | a0001c0017t0001g0134a0001c0017t0001g0135a0001c0017t0001g0144 | 3 | HG02976.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3793-392T>C | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176595140 | ||||||
chr5:176595309
|
G | A | 4 | a0003c0002t0001g0204a0003c0002t0001g0219a0003c0002t0001g0252others(1): Show | 4 | HG00323.hp1 HG00738.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.3793-223G>A | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176595309 | ||||||
chr5:176595312
|
A | G | 65 | a0001c0003t0001g0010a0001c0003t0001g0012a0001c0003t0001g0021others(62): Show | 72 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.3793-220A>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176595312 | ||||||
chr5:176595323
|
C | T | 4 | a0004c0009t0001g0146a0004c0009t0001g0147a0004c0009t0001g0312others(1): Show | 4 | HG01891.hp1 HG02559.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3793-209C>T | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176595323 | ||||||
chr5:176595520
|
C | G | 5 | a0001c0004t0001g0169a0001c0008t0001g0176a0001c0008t0001g0177others(2): Show | 5 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3793-12C>G | CDHR2 | ENSG00000074276.11 | transcript | ENST00000261944.10 | protein_coding | 31/31 | chr5 | 176595520 |