geneid | 4345 |
---|---|
ensemblid | ENSG00000091972.18 |
hgncid | 7203 |
symbol | CD200 |
name | CD200 molecule |
refseq_nuc | NM_005944.7 |
refseq_prot | NP_005935.4 |
ensembl_nuc | ENST00000315711.12 |
ensembl_prot | ENSP00000312766.8 |
mane_status | MANE Select |
chr | chr3 |
start | 112333156 |
end | 112362812 |
strand | + |
ver | v1.2 |
region | chr3:112333156-112362812 |
region5000 | chr3:112328156-112367812 |
regionname0 | CD200_chr3_112333156_112362812 |
regionname5000 | CD200_chr3_112328156_112367812 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 269 | 272 | 77 | 45 | 116 | 11 | 22 | 90 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0002 | 0/0 | 269 | 73 | 10 | 19 | 31 | 4 | 9 | 24 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0003 | 1/0 | 269 | 61 | 9 | 12 | 29 | 1 | 9 | 22 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0004 | 0/0 | 269 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 810 | 182 | 48 | 39 | 73 | 11 | 10 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
c0002 | 0/0 | 810 | 88 | 28 | 6 | 42 | 0 | 12 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
c0003 | 0/0 | 810 | 73 | 10 | 19 | 31 | 4 | 9 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
c0004 | 1/0 | 810 | 51 | 3 | 12 | 27 | 1 | 7 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
c0005 | 0/0 | 810 | 6 | 6 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
c0006 | 0/0 | 810 | 4 | 0 | 0 | 2 | 0 | 2 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
c0007 | 0/0 | 810 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
c0008 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
c0009 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1322 | 320 | 44 | 76 | 148 | 16 | 35 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0002 | 0/0 | 1322 | 35 | 16 | 1 | 17 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0003 | 0/0 | 1316 | 10 | 9 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0004 | 1/0 | 1320 | 9 | 8 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0005 | 0/0 | 1322 | 4 | 0 | 0 | 4 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0006 | 0/0 | 1322 | 4 | 3 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0007 | 0/0 | 1316 | 4 | 0 | 0 | 2 | 0 | 2 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0008 | 0/0 | 1322 | 3 | 3 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0009 | 0/0 | 1322 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0010 | 0/0 | 1316 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0011 | 0/0 | 1318 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0012 | 0/0 | 1322 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0013 | 0/0 | 1322 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0014 | 0/0 | 1322 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0015 | 0/0 | 1322 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0016 | 0/0 | 1322 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0017 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0018 | 0/0 | 1322 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0019 | 0/0 | 1322 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0020 | 0/0 | 1322 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0021 | 0/0 | 1322 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0022 | 0/0 | 1322 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0023 | 0/0 | 1322 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0024 | 0/0 | 1316 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
t0025 | 0/0 | 1318 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 1 | 0 | 8 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0002 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0004 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0005 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0008 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0181 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0267 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 810 | 182 | 48 | 39 | 73 | 11 | 10 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0002 | 0/0 | 810 | 88 | 28 | 6 | 42 | 0 | 12 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0008 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0009 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0002c0003 | 0/0 | 810 | 73 | 10 | 19 | 31 | 4 | 9 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0003c0004 | 1/0 | 810 | 51 | 3 | 12 | 27 | 1 | 7 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0003c0005 | 0/0 | 810 | 6 | 6 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0003c0006 | 0/0 | 810 | 4 | 0 | 0 | 2 | 0 | 2 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0004c0007 | 0/0 | 810 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2131 | 149 | 23 | 38 | 66 | 11 | 10 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0001t0002 | 0/0 | 2131 | 10 | 6 | 0 | 4 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0001t0003 | 0/0 | 2125 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0001t0004 | 0/0 | 2129 | 7 | 7 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0001t0006 | 0/0 | 2131 | 4 | 3 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0001t0008 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0001t0009 | 0/0 | 2131 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0001t0011 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0001t0013 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0001t0015 | 0/0 | 2131 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0001t0017 | 0/0 | 2129 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0001t0018 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0001t0024 | 0/0 | 2125 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0001t0025 | 0/0 | 2127 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0002t0001 | 0/0 | 2131 | 69 | 12 | 5 | 41 | 0 | 11 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0002t0002 | 0/0 | 2131 | 8 | 7 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0002t0003 | 0/0 | 2125 | 3 | 3 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0002t0004 | 0/0 | 2129 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0002t0014 | 0/0 | 2131 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0002t0016 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0002t0019 | 0/0 | 2131 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0002t0020 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0002t0021 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0002t0022 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0002t0023 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0008t0001 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0001c0009t0001 | 0/0 | 2131 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0002c0003t0001 | 0/0 | 2131 | 65 | 6 | 19 | 27 | 4 | 9 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0002c0003t0002 | 0/0 | 2131 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0002c0003t0005 | 0/0 | 2131 | 4 | 0 | 0 | 4 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0002c0003t0008 | 0/0 | 2131 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0003c0004t0001 | 0/0 | 2131 | 33 | 2 | 12 | 13 | 1 | 5 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0003c0004t0002 | 0/0 | 2131 | 15 | 1 | 0 | 13 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0003c0004t0003 | 0/0 | 2125 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0003c0004t0004 | 1/0 | 2129 | 1 | 0 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0003c0004t0012 | 0/0 | 2131 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0003c0005t0003 | 0/0 | 2125 | 4 | 4 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0003c0005t0010 | 0/0 | 2125 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0003c0006t0007 | 0/0 | 2125 | 4 | 0 | 0 | 2 | 0 | 2 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
a0004c0007t0001 | 0/0 | 2131 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | copy fasta | chr3 | 112328156 | 112367812 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0002 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0005 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0181 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0004g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0006g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0009g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0009g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0011g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0013g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0017g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0018g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0024g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0001t0025g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0014g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0016g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0019g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0020g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0021g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0022g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0002t0023g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0008t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0001c0009t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0005g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0002c0003t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0008 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0004g0267 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0004t0012g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0005t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0005t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0005t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0005t0010g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0005t0010g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0006t0007g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0006t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0006t0007g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0003c0006t0007g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
a0004c0007t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | GBR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00140 | hp2 | a0002 | c0003 | t0001 | g0332 | EUR | GBR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | FIN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | FIN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00323 | hp1 | a0002 | c0003 | t0001 | g0285 | EUR | FIN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00323 | hp2 | a0003 | c0004 | t0001 | g0008 | EUR | FIN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00438 | hp2 | a0003 | c0004 | t0002 | g0058 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00544 | hp1 | a0003 | c0006 | t0007 | g0198 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00544 | hp2 | a0002 | c0003 | t0001 | g0318 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00558 | hp1 | a0002 | c0003 | t0001 | g0325 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00597 | hp1 | a0002 | c0003 | t0001 | g0291 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00597 | hp2 | a0002 | c0003 | t0001 | g0308 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00609 | hp2 | a0003 | c0004 | t0002 | g0057 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00639 | hp2 | a0002 | c0003 | t0001 | g0328 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00673 | hp1 | a0002 | c0003 | t0001 | g0294 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00733 | hp1 | a0002 | c0003 | t0001 | g0284 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00738 | hp2 | a0003 | c0004 | t0001 | g0008 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00741 | hp1 | a0003 | c0004 | t0001 | g0022 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01074 | hp1 | a0002 | c0003 | t0001 | g0335 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0258 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01106 | hp1 | a0002 | c0003 | t0001 | g0039 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0105 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01109 | hp2 | a0003 | c0004 | t0001 | g0150 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01167 | hp2 | a0003 | c0004 | t0001 | g0023 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01168 | hp1 | a0003 | c0004 | t0001 | g0149 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01169 | hp2 | a0003 | c0004 | t0001 | g0023 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01175 | hp1 | a0002 | c0003 | t0001 | g0274 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01192 | hp1 | a0002 | c0003 | t0001 | g0278 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01256 | hp1 | a0004 | c0007 | t0001 | g0027 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01256 | hp2 | a0002 | c0003 | t0001 | g0319 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01257 | hp2 | a0003 | c0004 | t0001 | g0022 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01258 | hp1 | a0003 | c0004 | t0001 | g0008 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01258 | hp2 | a0004 | c0007 | t0001 | g0027 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01261 | hp2 | a0002 | c0003 | t0001 | g0316 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01346 | hp2 | a0002 | c0003 | t0001 | g0301 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01358 | hp2 | a0002 | c0003 | t0001 | g0275 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01361 | hp2 | a0003 | c0004 | t0001 | g0153 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01433 | hp1 | a0002 | c0003 | t0001 | g0295 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01516 | hp2 | a0002 | c0003 | t0001 | g0039 | EUR | IBS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01517 | hp2 | a0002 | c0003 | t0001 | g0320 | EUR | IBS | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0338 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0264 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01934 | hp2 | a0002 | c0003 | t0001 | g0283 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01943 | hp1 | a0002 | c0003 | t0001 | g0302 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01952 | hp1 | a0002 | c0003 | t0001 | g0333 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01978 | hp2 | a0003 | c0004 | t0001 | g0010 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01981 | hp2 | a0002 | c0003 | t0001 | g0282 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01993 | hp1 | a0002 | c0003 | t0001 | g0331 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02004 | hp1 | a0002 | c0003 | t0001 | g0304 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02004 | hp2 | a0002 | c0003 | t0001 | g0281 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02015 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02040 | hp2 | a0002 | c0003 | t0001 | g0321 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02055 | hp1 | a0002 | c0003 | t0001 | g0340 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02056 | hp2 | a0003 | c0004 | t0002 | g0053 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02074 | hp2 | a0003 | c0004 | t0002 | g0130 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02129 | hp1 | a0003 | c0004 | t0002 | g0054 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02129 | hp2 | a0003 | c0004 | t0003 | g0270 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02145 | hp1 | a0001 | c0002 | t0020 | g0182 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02148 | hp1 | a0003 | c0004 | t0001 | g0148 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | CDX | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02257 | hp1 | a0003 | c0005 | t0003 | g0021 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02258 | hp1 | a0002 | c0003 | t0001 | g0277 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02258 | hp2 | a0001 | c0002 | t0021 | g0101 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0269 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02451 | hp2 | a0001 | c0002 | t0022 | g0245 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02523 | hp2 | a0002 | c0003 | t0001 | g0334 | EAS | KHV | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02572 | hp1 | a0002 | c0003 | t0001 | g0339 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02572 | hp2 | a0001 | c0001 | t0017 | g0236 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02602 | hp1 | a0003 | c0004 | t0012 | g0016 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02602 | hp2 | a0002 | c0003 | t0001 | g0286 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02622 | hp1 | a0001 | c0002 | t0004 | g0089 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02622 | hp2 | a0001 | c0008 | t0001 | g0240 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02630 | hp1 | a0003 | c0005 | t0010 | g0127 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02630 | hp2 | a0001 | c0001 | t0008 | g0136 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0263 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02698 | hp1 | a0003 | c0004 | t0001 | g0154 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02698 | hp2 | a0002 | c0003 | t0001 | g0287 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02717 | hp2 | a0003 | c0005 | t0010 | g0128 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0167 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02735 | hp1 | a0003 | c0006 | t0007 | g0140 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02738 | hp1 | a0003 | c0004 | t0002 | g0016 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02809 | hp2 | a0001 | c0002 | t0003 | g0199 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0107 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02886 | hp1 | a0003 | c0005 | t0003 | g0133 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02896 | hp2 | a0002 | c0003 | t0008 | g0192 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02897 | hp2 | a0002 | c0003 | t0008 | g0190 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02922 | hp2 | a0001 | c0002 | t0023 | g0047 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02965 | hp1 | a0003 | c0005 | t0003 | g0021 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02970 | hp1 | a0002 | c0003 | t0002 | g0276 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02970 | hp2 | a0001 | c0001 | t0013 | g0178 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02976 | hp1 | a0001 | c0002 | t0003 | g0090 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0100 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03017 | hp2 | a0002 | c0003 | t0001 | g0323 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03041 | hp1 | a0003 | c0004 | t0001 | g0141 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0135 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0069 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0265 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0279 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03139 | hp1 | a0001 | c0002 | t0016 | g0051 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03195 | hp1 | a0002 | c0003 | t0002 | g0273 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03209 | hp2 | a0003 | c0004 | t0002 | g0260 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03225 | hp1 | a0001 | c0002 | t0003 | g0118 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0261 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03239 | hp1 | a0002 | c0003 | t0001 | g0341 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03453 | hp2 | a0002 | c0003 | t0001 | g0191 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03486 | hp1 | a0003 | c0005 | t0003 | g0134 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03491 | hp1 | a0002 | c0003 | t0001 | g0314 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | GWD | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0103 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03669 | hp1 | a0002 | c0003 | t0001 | g0329 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03688 | hp1 | a0003 | c0004 | t0001 | g0145 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0095 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03704 | hp1 | a0003 | c0004 | t0001 | g0151 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03710 | hp1 | a0002 | c0003 | t0001 | g0327 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03831 | hp2 | a0001 | c0002 | t0019 | g0113 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03834 | hp1 | a0003 | c0004 | t0001 | g0056 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03834 | hp2 | a0003 | c0004 | t0001 | g0132 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0094 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03927 | hp2 | a0002 | c0003 | t0001 | g0313 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0081 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0112 | SAS | BEB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG04204 | hp1 | a0003 | c0006 | t0007 | g0138 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG04228 | hp2 | a0002 | c0003 | t0001 | g0280 | SAS | STU | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | CHB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18906 | hp1 | a0003 | c0004 | t0001 | g0143 | AFR | YRI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18940 | hp2 | a0002 | c0003 | t0005 | g0038 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18942 | hp2 | a0003 | c0004 | t0001 | g0010 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18945 | hp1 | a0003 | c0004 | t0002 | g0060 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18946 | hp1 | a0003 | c0004 | t0002 | g0015 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18947 | hp1 | a0003 | c0004 | t0001 | g0297 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18947 | hp2 | a0002 | c0003 | t0001 | g0307 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18949 | hp1 | a0002 | c0003 | t0001 | g0322 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18952 | hp1 | a0003 | c0004 | t0002 | g0015 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18954 | hp1 | a0001 | c0001 | t0009 | g0222 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18956 | hp1 | a0003 | c0006 | t0007 | g0139 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18957 | hp1 | a0001 | c0002 | t0014 | g0097 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18959 | hp2 | a0002 | c0003 | t0001 | g0292 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18961 | hp1 | a0003 | c0004 | t0001 | g0296 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18963 | hp1 | a0002 | c0003 | t0001 | g0306 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18964 | hp2 | a0002 | c0003 | t0001 | g0293 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18968 | hp2 | a0002 | c0003 | t0005 | g0330 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18969 | hp2 | a0003 | c0004 | t0002 | g0063 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18970 | hp1 | a0002 | c0003 | t0001 | g0317 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18971 | hp1 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18974 | hp2 | a0003 | c0004 | t0001 | g0009 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18975 | hp1 | a0002 | c0003 | t0001 | g0300 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18977 | hp2 | a0003 | c0004 | t0002 | g0062 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18979 | hp1 | a0003 | c0004 | t0001 | g0147 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18979 | hp2 | a0002 | c0003 | t0001 | g0290 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18981 | hp1 | a0002 | c0003 | t0001 | g0303 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18981 | hp2 | a0001 | c0001 | t0009 | g0229 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18982 | hp1 | a0002 | c0003 | t0001 | g0310 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18982 | hp2 | a0003 | c0004 | t0001 | g0061 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18983 | hp1 | a0003 | c0004 | t0001 | g0193 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18983 | hp2 | a0002 | c0003 | t0001 | g0311 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18985 | hp1 | a0003 | c0004 | t0002 | g0131 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18986 | hp1 | a0003 | c0004 | t0001 | g0298 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19000 | hp1 | a0003 | c0004 | t0001 | g0152 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19000 | hp2 | a0002 | c0003 | t0001 | g0309 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19003 | hp1 | a0003 | c0004 | t0002 | g0055 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19004 | hp1 | a0003 | c0004 | t0001 | g0146 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19005 | hp2 | a0002 | c0003 | t0005 | g0315 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19006 | hp1 | a0002 | c0003 | t0001 | g0289 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19007 | hp1 | a0002 | c0003 | t0001 | g0324 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19007 | hp2 | a0003 | c0004 | t0002 | g0059 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19009 | hp2 | a0002 | c0003 | t0001 | g0312 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | LWK | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | LWK | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19043 | hp2 | a0001 | c0001 | t0025 | g0126 | AFR | LWK | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19056 | hp2 | a0002 | c0003 | t0001 | g0305 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19057 | hp1 | a0003 | c0004 | t0001 | g0009 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19060 | hp1 | a0003 | c0004 | t0001 | g0144 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19072 | hp2 | a0002 | c0003 | t0001 | g0288 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19076 | hp2 | a0001 | c0009 | t0001 | g0019 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19078 | hp1 | a0002 | c0003 | t0005 | g0326 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19082 | hp2 | a0002 | c0003 | t0001 | g0272 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19083 | hp1 | a0002 | c0003 | t0001 | g0299 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19088 | hp2 | a0003 | c0004 | t0001 | g0009 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA19240 | hp2 | a0001 | c0001 | t0024 | g0155 | AFR | YRI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | ASW | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | TSI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | TSI | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01123 | hp1 | a0003 | c0004 | t0001 | g0010 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG01123 | hp2 | a0002 | c0003 | t0001 | g0268 | AMR | CLM | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0216 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0129 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0071 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03471 | hp1 | a0001 | c0002 | t0002 | g0091 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | MSL | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG06807 | hp1 | a0002 | c0003 | t0001 | g0271 | AFR | USA | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | USA | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | USA | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | USA | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA21309 | hp1 | a0001 | c0001 | t0018 | g0213 | AFR | LWK | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0181 | REF | REF | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
homoSapiens_grch38 | hp1 | a0003 | c0004 | t0004 | g0267 | REF | REF | CD200_chr3_112328156_112367812 | CD200 | chr3 | 112328156 | 112367812 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:112340921
|
C | G | 2 | a0001a0004 | 274 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
missense_variant | MODERATE | c.32C>G | p.Ser11Cys | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/6 | 89/2129 | 32/810 | 11/269 | chr3 | 112340921 | ||
chr3:112345003
|
C | A | 1 | a0002 | 73 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(70): Show |
missense_variant | MODERATE | c.136C>A | p.Pro46Thr | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/6 | 193/2129 | 136/810 | 46/269 | chr3 | 112345003 | ||
chr3:112347599
|
C | T | 1 | a0004 | 2 | HG01256.hp1 HG01258.hp2 |
missense_variant | MODERATE | c.463C>T | p.His155Tyr | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/6 | 520/2129 | 463/810 | 155/269 | chr3 | 112347599 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:112345269
|
G | A | 2 | a0001c0008a0003c0006 | 5 | HG00544.hp1 HG02622.hp2 HG02735.hp1 others(2): Show |
synonymous_variant | LOW | c.402G>A | p.Thr134Thr | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/6 | 459/2129 | 402/810 | 134/269 | chr3 | 112345269 | ||
chr3:112347715
|
G | A | 3 | a0001c0002a0001c0009a0003c0005 | 95 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(92): Show |
synonymous_variant | LOW | c.579G>A | p.Thr193Thr | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/6 | 636/2129 | 579/810 | 193/269 | chr3 | 112347715 | ||
chr3:112347820
|
C | T | 1 | a0001c0009 | 1 | NA19076.hp2 | synonymous_variant | LOW | c.684C>T | p.Thr228Thr | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/6 | 741/2129 | 684/810 | 228/269 | chr3 | 112347820 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:112361551
|
A | C | 8 | a0001c0001t0003a0001c0001t0024a0001c0001t0025others(5): Show | 18 | HG00544.hp1 HG02129.hp2 HG02257.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1 | chr3 | 112361551 | |||||
chr3:112361699
|
C | A | 1 | a0003c0005t0010 | 2 | HG02630.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*149C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 149 | chr3 | 112361699 | |||||
chr3:112361719
|
T | C | 1 | a0002c0003t0005 | 4 | NA18940.hp2 NA18968.hp2 NA19005.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*169T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 169 | chr3 | 112361719 | |||||
chr3:112361797
|
T | C | 4 | a0001c0001t0003a0001c0002t0003a0003c0004t0003others(1): Show | 10 | HG02129.hp2 HG02257.hp1 HG02809.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*247T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 247 | chr3 | 112361797 | |||||
chr3:112361818
|
CTTAG | C | 9 | a0001c0001t0003a0001c0001t0011a0001c0001t0024others(6): Show | 19 | HG00544.hp1 HG02129.hp2 HG02257.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*274_*277delTAGT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 274 | INFO_REALIGN_3_PRIME | chr3 | 112361818 | ||||
chr3:112361842
|
G | A | 2 | a0001c0001t0008a0002c0003t0008 | 3 | HG02630.hp2 HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*292G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 292 | chr3 | 112361842 | |||||
chr3:112361870
|
G | C | 1 | a0003c0004t0012 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*320G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 320 | chr3 | 112361870 | |||||
chr3:112361882
|
G | C | 1 | a0001c0001t0009 | 2 | NA18954.hp1 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*332G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 332 | chr3 | 112361882 | |||||
chr3:112361999
|
G | A | 1 | a0001c0001t0013 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*449G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 449 | chr3 | 112361999 | |||||
chr3:112362159
|
G | A | 1 | a0001c0002t0014 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*609G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 609 | chr3 | 112362159 | |||||
chr3:112362182
|
A | G | 1 | a0001c0002t0023 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*632A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 632 | chr3 | 112362182 | |||||
chr3:112362247
|
A | C | 1 | a0001c0001t0025 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*697A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 697 | chr3 | 112362247 | |||||
chr3:112362318
|
C | A | 1 | a0001c0001t0015 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*768C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 768 | chr3 | 112362318 | |||||
chr3:112362348
|
C | T | 7 | a0001c0001t0003a0001c0001t0024a0001c0002t0003others(4): Show | 17 | HG00544.hp1 HG02129.hp2 HG02257.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*798C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 798 | chr3 | 112362348 | |||||
chr3:112362352
|
C | A | 1 | a0001c0002t0016 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*802C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 802 | chr3 | 112362352 | |||||
chr3:112362511
|
G | A | 6 | a0001c0001t0002a0001c0001t0017a0001c0002t0002others(3): Show | 37 | HG00438.hp2 HG00609.hp2 HG01106.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*961G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 961 | chr3 | 112362511 | |||||
chr3:112362513
|
G | A | 1 | a0001c0001t0018 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*963G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 963 | chr3 | 112362513 | |||||
chr3:112362538
|
G | A | 2 | a0001c0001t0024a0003c0005t0010 | 3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*988G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 988 | chr3 | 112362538 | |||||
chr3:112362550
|
C | T | 1 | a0001c0002t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1000C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1000 | chr3 | 112362550 | |||||
chr3:112362667
|
G | T | 1 | a0001c0002t0021 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1117G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1117 | chr3 | 112362667 | |||||
chr3:112362672
|
G | A | 1 | a0001c0002t0019 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1122G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1122 | chr3 | 112362672 | |||||
chr3:112362696
|
G | C | 7 | a0001c0001t0003a0001c0001t0024a0001c0002t0003others(4): Show | 17 | HG00544.hp1 HG02129.hp2 HG02257.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1146G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1146 | chr3 | 112362696 | |||||
chr3:112362713
|
T | TTA | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(26): Show | 381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
3_prime_UTR_variant | MODIFIER | c.*1176_*1177dupTA | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1178 | INFO_REALIGN_3_PRIME | chr3 | 112362713 | ||||
chr3:112362754
|
C | A | 1 | a0001c0002t0020 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1204C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1204 | chr3 | 112362754 | |||||
chr3:112362790
|
C | A | 1 | a0001c0001t0006 | 4 | HG01081.hp2 HG01891.hp2 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1240C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 6/6 | 1240 | chr3 | 112362790 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:112333256
|
G | T | 77 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0002t0001g0269others(74): Show | 78 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.12+32G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333256 | ||||||
chr3:112333273
|
G | A | 6 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(3): Show | 6 | HG00280.hp1 HG00738.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+49G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333273 | ||||||
chr3:112333288
|
GGGCGGGC others(11): Show |
G | 1 | a0002c0003t0001g0268 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.12+69_12+86delGGCG others(14): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 112333288 | |||||
chr3:112333291
|
C | A | 1 | a0001c0001t0001g0014 | 2 | NA19006.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.12+67C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333291 | ||||||
chr3:112333309
|
C | A | 1 | a0002c0003t0001g0268 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.12+85C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333309 | ||||||
chr3:112333312
|
G | C | 1 | a0002c0003t0001g0268 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.12+88G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333312 | ||||||
chr3:112333313
|
G | C | 1 | a0002c0003t0001g0268 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.12+89G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333313 | ||||||
chr3:112333326
|
T | C | 336 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(333): Show | 398 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(395): Show |
intron_variant | MODIFIER | c.12+102T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333326 | ||||||
chr3:112333798
|
T | C | 2 | a0001c0002t0002g0046a0001c0002t0023g0047 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.12+574T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333798 | ||||||
chr3:112333961
|
G | A | 1 | a0001c0001t0006g0258 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.12+737G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333961 | ||||||
chr3:112333986
|
G | A | 95 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0122others(92): Show | 103 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.12+762G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112333986 | ||||||
chr3:112334080
|
G | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.12+856G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112334080 | ||||||
chr3:112334237
|
CA | C | 4 | a0001c0002t0001g0129a0001c0002t0001g0269a0001c0002t0002g0046others(1): Show | 4 | HG02109.hp2 HG02451.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+1014delA | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112334237 | ||||||
chr3:112334399
|
T | C | 167 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0122others(164): Show | 176 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.12+1175T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112334399 | ||||||
chr3:112334718
|
G | A | 131 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(128): Show | 147 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.12+1494G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112334718 | ||||||
chr3:112334748
|
G | GA | 7 | a0001c0001t0001g0125a0001c0002t0001g0048a0001c0002t0001g0049others(4): Show | 7 | HG02055.hp2 HG02074.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.12+1534dupA | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 112334748 | |||||
chr3:112334748
|
GA | G | 66 | a0001c0001t0001g0336a0001c0001t0001g0337a0002c0003t0001g0038others(63): Show | 67 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.12+1534delA | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 112334748 | |||||
chr3:112334758
|
AC | A | 5 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(2): Show | 5 | NA18970.hp2 NA18974.hp1 NA19072.hp1 others(2): Show |
intron_variant | MODIFIER | c.12+1536delC | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 112334758 | |||||
chr3:112334759
|
C | A | 6 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0189others(3): Show | 6 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.12+1535C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112334759 | ||||||
chr3:112334904
|
C | T | 131 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(128): Show | 147 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.12+1680C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112334904 | ||||||
chr3:112335236
|
A | C | 2 | a0001c0002t0002g0046a0001c0002t0023g0047 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.12+2012A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335236 | ||||||
chr3:112335277
|
T | C | 6 | a0001c0001t0001g0137a0001c0001t0004g0135a0001c0001t0008g0136others(3): Show | 7 | HG02257.hp1 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+2053T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335277 | ||||||
chr3:112335371
|
A | G | 2 | a0001c0002t0001g0129a0001c0002t0001g0269 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.12+2147A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335371 | ||||||
chr3:112335376
|
C | G | 3 | a0001c0001t0024g0155a0003c0005t0010g0127a0003c0005t0010g0128 | 3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.12+2152C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335376 | ||||||
chr3:112335387
|
T | C | 6 | a0001c0001t0001g0137a0001c0001t0004g0135a0001c0001t0008g0136others(3): Show | 7 | HG02257.hp1 HG02630.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.12+2163T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335387 | ||||||
chr3:112335389
|
G | A | 8 | a0002c0003t0001g0280a0002c0003t0001g0281a0002c0003t0001g0282others(5): Show | 8 | HG00323.hp1 HG00733.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.12+2165G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335389 | ||||||
chr3:112335408
|
G | A | 3 | a0002c0003t0001g0191a0002c0003t0008g0190a0002c0003t0008g0192 | 3 | HG02896.hp2 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.12+2184G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335408 | ||||||
chr3:112335666
|
A | ACAT | 4 | a0001c0001t0001g0125a0001c0001t0024g0155a0003c0005t0010g0127others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+2446_12+2448dup others(3): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 112335666 | |||||
chr3:112335678
|
C | G | 1 | a0001c0002t0001g0124 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.12+2454C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335678 | ||||||
chr3:112335688
|
T | C | 3 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140 | 3 | HG02735.hp1 HG04204.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.12+2464T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335688 | ||||||
chr3:112335730
|
A | G | 1 | a0001c0002t0001g0124 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.12+2506A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335730 | ||||||
chr3:112335804
|
A | T | 4 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(1): Show | 4 | NA18970.hp2 NA19072.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.12+2580A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112335804 | ||||||
chr3:112336092
|
T | C | 1 | a0001c0001t0024g0155 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.12+2868T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336092 | ||||||
chr3:112336117
|
C | G | 1 | a0001c0001t0001g0252 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.12+2893C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336117 | ||||||
chr3:112336176
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(97): Show | 136 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.12+2952G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336176 | ||||||
chr3:112336269
|
C | T | 1 | a0002c0003t0001g0341 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.12+3045C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336269 | ||||||
chr3:112336308
|
G | C | 17 | a0001c0001t0001g0137a0001c0001t0001g0262a0001c0001t0001g0266others(14): Show | 18 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.12+3084G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336308 | ||||||
chr3:112336370
|
C | T | 3 | a0001c0001t0024g0155a0003c0005t0010g0127a0003c0005t0010g0128 | 3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.12+3146C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336370 | ||||||
chr3:112336525
|
C | T | 1 | a0001c0002t0023g0047 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.12+3301C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336525 | ||||||
chr3:112336686
|
TACAA | T | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 407 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(404): Show |
intron_variant | MODIFIER | c.12+3467_12+3470del others(4): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr3 | 112336686 | |||||
chr3:112336789
|
G | T | 3 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140 | 3 | HG02735.hp1 HG04204.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.12+3565G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336789 | ||||||
chr3:112336790
|
G | C | 1 | a0001c0002t0001g0259 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.12+3566G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336790 | ||||||
chr3:112336864
|
G | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(100): Show | 139 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.12+3640G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336864 | ||||||
chr3:112336946
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 283 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.12+3722A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336946 | ||||||
chr3:112336989
|
A | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG01257.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.12+3765A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336989 | ||||||
chr3:112336992
|
A | T | 75 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0002t0002g0279others(72): Show | 76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.12+3768A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112336992 | ||||||
chr3:112337105
|
A | G | 37 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(34): Show | 44 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.13-3797A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112337105 | ||||||
chr3:112337567
|
A | G | 326 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(323): Show | 380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.13-3335A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112337567 | ||||||
chr3:112337661
|
G | C | 2 | a0001c0002t0001g0129a0001c0002t0001g0269 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.13-3241G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112337661 | ||||||
chr3:112337664
|
T | A | 1 | a0001c0001t0001g0125 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.13-3238T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112337664 | ||||||
chr3:112337784
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0024g0155a0003c0005t0010g0127others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-3118C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112337784 | ||||||
chr3:112338070
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.13-2832A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338070 | ||||||
chr3:112338087
|
A | G | 326 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(323): Show | 380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.13-2815A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338087 | ||||||
chr3:112338183
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.13-2719G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338183 | ||||||
chr3:112338261
|
G | A | 1 | a0001c0002t0001g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.13-2641G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338261 | ||||||
chr3:112338288
|
T | C | 131 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(128): Show | 147 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.13-2614T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338288 | ||||||
chr3:112338289
|
G | A | 1 | a0001c0002t0016g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.13-2613G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338289 | ||||||
chr3:112338346
|
G | A | 9 | a0001c0001t0001g0262a0001c0001t0001g0266a0001c0001t0006g0258others(6): Show | 9 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.13-2556G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338346 | ||||||
chr3:112338388
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.13-2514C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338388 | ||||||
chr3:112338728
|
G | A | 3 | a0001c0001t0024g0155a0003c0005t0010g0127a0003c0005t0010g0128 | 3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.13-2174G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338728 | ||||||
chr3:112338766
|
C | CAAT | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 154 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.13-2136_13-2135ins others(3): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112338766 | ||||||
chr3:112339191
|
A | G | 16 | a0001c0001t0001g0137a0001c0001t0001g0262a0001c0001t0001g0266others(13): Show | 17 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.13-1711A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339191 | ||||||
chr3:112339255
|
A | G | 1 | a0003c0004t0001g0153 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.13-1647A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339255 | ||||||
chr3:112339298
|
T | C | 1 | a0001c0002t0001g0052 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.13-1604T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339298 | ||||||
chr3:112339401
|
G | A | 1 | a0003c0004t0001g0141 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.13-1501G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339401 | ||||||
chr3:112339581
|
G | A | 2 | a0003c0005t0010g0127a0003c0005t0010g0128 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.13-1321G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339581 | ||||||
chr3:112339604
|
G | C | 12 | a0002c0003t0001g0288a0002c0003t0001g0289a0002c0003t0001g0290others(9): Show | 12 | HG00597.hp1 HG00673.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.13-1298G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339604 | ||||||
chr3:112339875
|
G | A | 1 | a0001c0001t0003g0024 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.13-1027G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339875 | ||||||
chr3:112339945
|
A | G | 3 | a0002c0003t0001g0338a0002c0003t0001g0339a0002c0003t0001g0340 | 3 | HG01884.hp1 HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.13-957A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339945 | ||||||
chr3:112339971
|
G | C | 3 | a0001c0001t0024g0155a0003c0005t0010g0127a0003c0005t0010g0128 | 3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.13-931G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112339971 | ||||||
chr3:112340063
|
A | G | 3 | a0001c0001t0024g0155a0003c0005t0010g0127a0003c0005t0010g0128 | 3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.13-839A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340063 | ||||||
chr3:112340076
|
A | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 134 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.13-826A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340076 | ||||||
chr3:112340187
|
A | G | 1 | a0001c0002t0001g0119 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.13-715A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340187 | ||||||
chr3:112340260
|
T | C | 1 | a0002c0003t0001g0300 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.13-642T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340260 | ||||||
chr3:112340281
|
T | A | 2 | a0001c0002t0001g0129a0001c0002t0001g0269 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.13-621T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340281 | ||||||
chr3:112340286
|
A | C | 1 | a0002c0003t0001g0299 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.13-616A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340286 | ||||||
chr3:112340287
|
G | A | 1 | a0002c0003t0001g0299 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.13-615G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340287 | ||||||
chr3:112340288
|
A | G | 1 | a0002c0003t0001g0299 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.13-614A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340288 | ||||||
chr3:112340365
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.13-537C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340365 | ||||||
chr3:112340366
|
G | A | 75 | a0001c0001t0001g0336a0001c0001t0001g0337a0001c0002t0002g0279others(72): Show | 76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.13-536G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340366 | ||||||
chr3:112340531
|
T | G | 2 | a0001c0002t0001g0129a0001c0002t0001g0269 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.13-371T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340531 | ||||||
chr3:112340736
|
A | G | 22 | a0001c0001t0001g0137a0001c0001t0001g0262a0001c0001t0001g0266others(19): Show | 24 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.13-166A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 1/5 | chr3 | 112340736 | ||||||
chr3:112341207
|
T | A | 4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+224T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112341207 | ||||||
chr3:112341399
|
G | A | 4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+416G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112341399 | ||||||
chr3:112341409
|
A | C | 76 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(73): Show | 83 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.94+426A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112341409 | ||||||
chr3:112341488
|
C | T | 4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+505C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112341488 | ||||||
chr3:112341541
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.94+558C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112341541 | ||||||
chr3:112341911
|
T | C | 175 | a0001c0001t0024g0155a0001c0002t0001g0006a0001c0002t0001g0007others(172): Show | 185 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.94+928T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112341911 | ||||||
chr3:112342043
|
A | G | 1 | a0001c0002t0001g0117 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.94+1060A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342043 | ||||||
chr3:112342048
|
T | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG02015.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.94+1065T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342048 | ||||||
chr3:112342064
|
A | G | 3 | a0001c0002t0001g0129a0001c0002t0001g0269a0001c0002t0020g0182 | 3 | HG02109.hp2 HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.94+1081A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342064 | ||||||
chr3:112342066
|
C | A | 1 | a0001c0001t0024g0155 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.94+1083C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342066 | ||||||
chr3:112342271
|
G | GTCCTTCC others(5): Show |
1 | a0001c0001t0001g0174 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.94+1314_94+1325dup others(12): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342271 | |||||
chr3:112342301
|
CCTTCCTT others(24): Show |
C | 1 | a0003c0006t0007g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.94+1322_94+1352del others(31): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342301 | |||||
chr3:112342301
|
CCTTCCTT others(32): Show |
C | 1 | a0003c0006t0007g0198 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.94+1322_94+1360del others(39): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342301 | |||||
chr3:112342301
|
CCTTCCTT others(36): Show |
C | 1 | a0003c0006t0007g0138 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.94+1322_94+1364del others(43): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342301 | |||||
chr3:112342303
|
TTCCTTTC others(28): Show |
T | 1 | a0003c0006t0007g0139 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.94+1322_94+1356del others(35): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342303 | |||||
chr3:112342305
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.94+1322C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342305 | ||||||
chr3:112342305
|
CCTTTCTT others(32): Show |
C | 1 | a0001c0001t0001g0242 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.94+1330_94+1368del others(39): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342305 | |||||
chr3:112342305
|
CCTTTCTT others(36): Show |
C | 2 | a0001c0001t0001g0241a0003c0004t0001g0154 | 2 | HG02698.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.94+1330_94+1372del others(43): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342305 | |||||
chr3:112342305
|
CCTTTCTT others(40): Show |
C | 1 | a0001c0001t0001g0037 | 2 | HG03239.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.94+1330_94+1376del others(47): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342305 | |||||
chr3:112342305
|
CCTTTCTT others(44): Show |
C | 1 | a0001c0001t0001g0013 | 3 | NA18957.hp2 NA19004.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.94+1330_94+1380del others(51): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342305 | |||||
chr3:112342305
|
CCTTTCTT others(48): Show |
C | 1 | a0003c0004t0001g0298 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.94+1330_94+1384del others(55): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342305 | |||||
chr3:112342306
|
C | CTTCCTTC others(25): Show |
1 | a0001c0001t0006g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+1325_94+1326ins others(32): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342306 | |||||
chr3:112342306
|
CTTTCTTC others(5): Show |
C | 1 | a0002c0003t0005g0315 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.94+1326_94+1337del others(12): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342306 | |||||
chr3:112342306
|
CTTTCTTC others(33): Show |
C | 2 | a0001c0001t0002g0120a0001c0001t0002g0121 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.94+1326_94+1365del others(40): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342306 | |||||
chr3:112342306
|
CTTTCTTC others(37): Show |
C | 1 | a0001c0001t0002g0123 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.94+1326_94+1369del others(44): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342306 | |||||
chr3:112342306
|
CTTTCTTC others(41): Show |
C | 1 | a0001c0001t0001g0122 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.94+1326_94+1373del others(48): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342306 | |||||
chr3:112342306
|
CTTTCTTC others(61): Show |
C | 1 | a0001c0001t0001g0243 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.94+1326_94+1393del others(68): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342306 | |||||
chr3:112342309
|
T | C | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(289): Show | 342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.94+1326T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342309 | ||||||
chr3:112342313
|
C | CCTTCCTT others(9): Show |
1 | a0001c0001t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94+1330_94+1331ins others(16): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | ||||||
chr3:112342313
|
C | T | 3 | a0001c0002t0001g0269a0003c0004t0001g0141a0003c0004t0001g0143 | 3 | HG02451.hp1 HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.94+1330C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | ||||||
chr3:112342313
|
CTTT | C | 21 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0041others(18): Show | 23 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.94+1331_94+1333del others(3): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | ||||||
chr3:112342313
|
CTTTCTTT | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0163a0001c0001t0001g0171others(3): Show | 7 | HG00642.hp2 HG00735.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1331_94+1337del others(7): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | ||||||
chr3:112342313
|
CTTTCTTT others(4): Show |
C | 8 | a0001c0001t0001g0029a0001c0001t0001g0044a0001c0001t0001g0137others(5): Show | 10 | HG00733.hp2 HG01192.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+1331_94+1341del others(11): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | ||||||
chr3:112342313
|
CTTTCTTT others(8): Show |
C | 5 | a0001c0001t0001g0043a0001c0001t0001g0125a0001c0001t0001g0248others(2): Show | 5 | HG00735.hp2 HG01981.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+1331_94+1345del others(15): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | ||||||
chr3:112342313
|
CTTTCTTT others(20): Show |
C | 10 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0004g0036others(7): Show | 12 | HG02080.hp1 HG02165.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+1331_94+1357del others(27): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | ||||||
chr3:112342313
|
CTTTCTTT others(24): Show |
C | 17 | a0001c0001t0001g0005a0001c0001t0001g0065a0001c0001t0001g0212others(14): Show | 20 | HG00323.hp1 HG01175.hp1 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.94+1331_94+1361del others(31): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | ||||||
chr3:112342313
|
CTTTCTTT others(28): Show |
C | 18 | a0001c0001t0001g0035a0001c0001t0001g0064a0001c0001t0001g0201others(15): Show | 19 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(16): Show |
intron_variant | MODIFIER | c.94+1331_94+1365del others(35): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | ||||||
chr3:112342313
|
CTTTCTTT others(32): Show |
C | 20 | a0001c0001t0001g0012a0001c0001t0001g0207a0001c0001t0001g0230others(17): Show | 26 | HG00609.hp1 HG00741.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.94+1331_94+1369del others(39): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | ||||||
chr3:112342313
|
CTTTCTTT others(35): Show |
C | 1 | a0001c0001t0001g0188 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.94+1332_94+1373del others(42): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342313 | |||||
chr3:112342313
|
CTTTCTTT others(36): Show |
C | 33 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0033others(30): Show | 47 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.94+1331_94+1373del others(43): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | ||||||
chr3:112342313
|
CTTTCTTT others(38): Show |
C | 1 | a0001c0001t0001g0189 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.94+1333_94+1377del others(45): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342313 | |||||
chr3:112342313
|
CTTTCTTT others(40): Show |
C | 21 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0185others(18): Show | 28 | HG00140.hp1 HG02040.hp1 HG02083.hp1 others(25): Show |
intron_variant | MODIFIER | c.94+1331_94+1377del others(47): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | ||||||
chr3:112342313
|
CTTTCTTT others(44): Show |
C | 16 | a0001c0001t0001g0011a0001c0001t0001g0219a0001c0001t0001g0220others(13): Show | 18 | HG01071.hp1 HG01928.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+1331_94+1381del others(51): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | ||||||
chr3:112342313
|
CTTTCTTT others(48): Show |
C | 10 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0218others(7): Show | 15 | HG00438.hp1 HG01106.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.94+1331_94+1385del others(55): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342313 | ||||||
chr3:112342314
|
T | C | 106 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(103): Show | 111 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.94+1331T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342314 | ||||||
chr3:112342317
|
C | T | 4 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG01346.hp1 HG02738.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+1334C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342317 | ||||||
chr3:112342317
|
CTTTCTTT others(16): Show |
C | 14 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0251others(11): Show | 14 | HG00673.hp1 HG01358.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.94+1335_94+1357del others(23): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342317 | ||||||
chr3:112342318
|
T | C | 87 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(84): Show | 92 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.94+1335T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342318 | ||||||
chr3:112342319
|
T | C | 1 | a0003c0004t0002g0260 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.94+1336T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342319 | ||||||
chr3:112342319
|
TTCTTTCT others(31): Show |
T | 1 | a0001c0001t0001g0217 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.94+1338_94+1375del others(38): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342319 | |||||
chr3:112342320
|
T | C | 18 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0041others(15): Show | 20 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.94+1337T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342320 | ||||||
chr3:112342321
|
C | CCTTCCTT others(5): Show |
1 | a0001c0001t0006g0258 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.94+1338_94+1339ins others(12): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342321 | ||||||
chr3:112342321
|
C | T | 1 | a0001c0001t0001g0028 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.94+1338C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342321 | ||||||
chr3:112342321
|
CTTTCTTT others(12): Show |
C | 2 | a0001c0001t0001g0203a0001c0001t0011g0167 | 2 | HG02071.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.94+1339_94+1357del others(19): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342321 | ||||||
chr3:112342321
|
CTTTCTTT others(14): Show |
C | 2 | a0001c0001t0001g0256a0001c0008t0001g0240 | 2 | HG02622.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.94+1341_94+1361del others(21): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342321 | |||||
chr3:112342321
|
CTTTCTTT others(18): Show |
C | 1 | a0001c0001t0001g0194 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.94+1341_94+1365del others(25): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342321 | |||||
chr3:112342322
|
T | C | 80 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(77): Show | 85 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.94+1339T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342322 | ||||||
chr3:112342322
|
TTTCTTTC others(9): Show |
T | 1 | a0003c0004t0001g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.94+1355_94+1370del others(16): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342322 | |||||
chr3:112342324
|
T | C | 21 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0041others(18): Show | 23 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.94+1341T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342324 | ||||||
chr3:112342325
|
C | CCTTT | 3 | a0001c0001t0001g0042a0001c0001t0001g0166a0001c0001t0006g0263 | 3 | HG01496.hp1 HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.94+1342_94+1343ins others(4): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342325 | ||||||
chr3:112342325
|
C | T | 2 | a0001c0001t0001g0173a0001c0002t0002g0046 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.94+1342C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342325 | ||||||
chr3:112342325
|
CT | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0045a0001c0001t0001g0176 | 4 | HG00738.hp1 HG01081.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+1345delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342325 | |||||
chr3:112342325
|
CTTTCTTT others(8): Show |
C | 10 | a0001c0001t0024g0155a0001c0002t0001g0073a0001c0002t0004g0089others(7): Show | 10 | HG01433.hp1 HG02074.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+1343_94+1357del others(15): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342325 | ||||||
chr3:112342326
|
T | C | 67 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0162others(64): Show | 70 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.94+1343T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342326 | ||||||
chr3:112342328
|
T | C | 22 | a0001c0001t0001g0029a0001c0001t0001g0040a0001c0001t0001g0041others(19): Show | 25 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.94+1345T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342328 | ||||||
chr3:112342329
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0162a0001c0001t0004g0135 | 4 | HG01255.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+1346C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342329 | ||||||
chr3:112342329
|
CT | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0172a0001c0001t0001g0175others(4): Show | 8 | HG00642.hp2 HG00735.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+1349delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342329 | |||||
chr3:112342329
|
CTTTCTTT others(4): Show |
C | 1 | a0001c0002t0001g0049 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.94+1347_94+1357del others(11): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342329 | ||||||
chr3:112342330
|
T | C | 63 | a0001c0001t0001g0025a0001c0001t0001g0142a0001c0001t0001g0162others(60): Show | 66 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.94+1347T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342330 | ||||||
chr3:112342332
|
T | C | 16 | a0001c0001t0001g0043a0001c0001t0001g0125a0001c0001t0001g0137others(13): Show | 17 | HG00735.hp2 HG01175.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+1349T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342332 | ||||||
chr3:112342333
|
C | T | 1 | a0001c0001t0006g0261 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.94+1350C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342333 | ||||||
chr3:112342333
|
CT | C | 10 | a0001c0001t0001g0029a0001c0001t0001g0040a0001c0001t0001g0041others(7): Show | 12 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+1353delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342333 | |||||
chr3:112342334
|
T | C | 61 | a0001c0001t0001g0142a0001c0001t0001g0174a0001c0001t0006g0258others(58): Show | 63 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.94+1351T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342334 | ||||||
chr3:112342335
|
T | C | 2 | a0002c0003t0001g0271a0002c0003t0008g0190 | 2 | HG02897.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.94+1352T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342335 | ||||||
chr3:112342336
|
TC | T | 11 | a0001c0001t0001g0043a0001c0001t0001g0125a0001c0001t0001g0137others(8): Show | 11 | HG00735.hp2 HG01192.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+1355delC | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342336 | |||||
chr3:112342337
|
C | T | 25 | a0001c0002t0020g0182a0002c0003t0001g0039a0002c0003t0001g0268others(22): Show | 27 | HG00544.hp2 HG00558.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.94+1354C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342337 | ||||||
chr3:112342337
|
CCTTCT | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0248a0002c0003t0001g0338others(1): Show | 5 | HG01175.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+1355_94+1359del others(5): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342337 | ||||||
chr3:112342337
|
CCTTCTTT others(7): Show |
C | 1 | a0002c0003t0001g0314 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.94+1355_94+1368del others(14): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342337 | ||||||
chr3:112342338
|
C | CTTCTTTC others(1): Show |
3 | a0003c0004t0001g0061a0003c0004t0002g0062a0003c0004t0002g0260 | 3 | HG03209.hp2 NA18977.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.94+1441_94+1448dup others(8): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | |||||
chr3:112342338
|
C | CTTCTTTC others(9): Show |
1 | a0003c0004t0002g0063 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.94+1433_94+1448dup others(16): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | |||||
chr3:112342338
|
C | CTTCTTTC others(17): Show |
1 | a0003c0004t0002g0131 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.94+1425_94+1448dup others(24): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | |||||
chr3:112342338
|
C | T | 34 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0029others(31): Show | 40 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.94+1355C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342338 | ||||||
chr3:112342338
|
CTTCT | C | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0003c0004t0001g0152others(1): Show | 4 | HG02074.hp2 HG02738.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+1445_94+1448del others(4): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | |||||
chr3:112342338
|
CTTCTTTC others(1): Show |
C | 7 | a0001c0001t0001g0181a0001c0001t0013g0178a0003c0004t0001g0132others(4): Show | 7 | HG00438.hp2 HG00609.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1441_94+1448del others(8): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | |||||
chr3:112342338
|
CTTCTTTC others(5): Show |
C | 4 | a0003c0004t0001g0010a0003c0004t0001g0056a0003c0004t0001g0193others(1): Show | 6 | HG01123.hp1 HG01978.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+1437_94+1448del others(12): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | |||||
chr3:112342338
|
CTTCTTTC others(9): Show |
C | 5 | a0001c0001t0001g0177a0003c0004t0001g0009a0003c0004t0001g0148others(2): Show | 7 | HG01168.hp1 HG01346.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+1433_94+1448del others(16): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | |||||
chr3:112342338
|
CTTCTTTC others(13): Show |
C | 7 | a0003c0004t0001g0023a0003c0004t0001g0145a0003c0004t0001g0146others(4): Show | 9 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+1429_94+1448del others(20): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | |||||
chr3:112342338
|
CTTCTTTC others(17): Show |
C | 1 | a0003c0004t0001g0008 | 3 | HG00323.hp2 HG00738.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.94+1425_94+1448del others(24): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | |||||
chr3:112342338
|
CTTCTTTC others(21): Show |
C | 1 | a0003c0004t0001g0022 | 2 | HG00741.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.94+1421_94+1448del others(28): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | |||||
chr3:112342338
|
CTTCTTTC others(33): Show |
C | 1 | a0003c0004t0001g0144 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.94+1409_94+1448del others(40): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342338 | |||||
chr3:112342341
|
C | T | 17 | a0001c0002t0003g0199a0002c0003t0001g0038a0002c0003t0001g0291others(14): Show | 17 | HG00597.hp1 HG00597.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.94+1358C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342341 | ||||||
chr3:112342341
|
CTTT | C | 5 | a0002c0003t0001g0288a0002c0003t0001g0289a0002c0003t0001g0290others(2): Show | 5 | NA18975.hp1 NA18979.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+1359_94+1361del others(3): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342341 | ||||||
chr3:112342341
|
CTTTCTTT others(8): Show |
C | 3 | a0002c0003t0001g0272a0002c0003t0001g0301a0002c0003t0001g0302 | 3 | HG01346.hp2 HG01943.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.94+1359_94+1373del others(15): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342341 | ||||||
chr3:112342341
|
CTTTCTTT others(27): Show |
C | 1 | a0001c0002t0001g0117 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.94+1360_94+1393del others(34): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342341 | |||||
chr3:112342341
|
CTTTCTTT others(36): Show |
C | 1 | a0001c0002t0001g0068 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.94+1359_94+1401del others(43): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342341 | ||||||
chr3:112342341
|
CTTTCTTT others(40): Show |
C | 1 | a0001c0002t0001g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.94+1359_94+1405del others(47): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342341 | ||||||
chr3:112342342
|
T | C | 25 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0004g0135others(22): Show | 27 | HG00597.hp1 HG00597.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.94+1359T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342342 | ||||||
chr3:112342344
|
T | C | 28 | a0001c0001t0008g0136a0001c0001t0024g0155a0001c0002t0001g0017others(25): Show | 29 | HG00673.hp1 HG01358.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.94+1361T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342344 | ||||||
chr3:112342345
|
CT | C | 8 | a0001c0001t0001g0203a0001c0001t0001g0214a0001c0001t0001g0215others(5): Show | 9 | HG02071.hp2 HG02723.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+1365delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342345 | |||||
chr3:112342345
|
CTTTCTTT others(6): Show |
C | 1 | a0002c0003t0001g0291 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.94+1365_94+1377del others(13): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342345 | |||||
chr3:112342346
|
T | C | 17 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0031others(14): Show | 20 | HG00738.hp1 HG01071.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.94+1363T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342346 | ||||||
chr3:112342348
|
T | C | 36 | a0001c0001t0001g0212a0001c0001t0001g0242a0001c0001t0001g0250others(33): Show | 37 | HG00323.hp1 HG00673.hp1 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.94+1365T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342348 | ||||||
chr3:112342349
|
C | T | 1 | a0003c0006t0007g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.94+1366C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342349 | ||||||
chr3:112342349
|
CT | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0065a0001c0001t0001g0235others(11): Show | 17 | HG01433.hp1 HG01928.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.94+1369delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342349 | |||||
chr3:112342350
|
T | C | 27 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0031others(24): Show | 30 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.94+1367T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342350 | ||||||
chr3:112342352
|
T | C | 38 | a0001c0001t0001g0202a0001c0001t0001g0208a0001c0001t0001g0209others(35): Show | 39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.94+1369T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342352 | ||||||
chr3:112342353
|
C | T | 1 | a0003c0006t0007g0139 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.94+1370C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342353 | ||||||
chr3:112342353
|
CT | C | 15 | a0001c0001t0001g0035a0001c0001t0001g0064a0001c0001t0001g0201others(12): Show | 16 | HG00408.hp1 HG00408.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.94+1373delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342353 | |||||
chr3:112342354
|
T | C | 29 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0030others(26): Show | 32 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.94+1371T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342354 | ||||||
chr3:112342354
|
TTTCTTTC others(4): Show |
T | 1 | a0003c0005t0003g0133 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.94+1374_94+1384del others(11): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342354 | |||||
chr3:112342356
|
T | C | 36 | a0001c0001t0001g0037a0001c0001t0001g0202a0001c0001t0001g0207others(33): Show | 43 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.94+1373T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342356 | ||||||
chr3:112342357
|
C | T | 2 | a0003c0005t0003g0021a0003c0006t0007g0198 | 3 | HG00544.hp1 HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.94+1374C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342357 | ||||||
chr3:112342357
|
CT | C | 23 | a0001c0001t0001g0012a0001c0001t0001g0208a0001c0001t0001g0209others(20): Show | 24 | HG00673.hp1 HG00673.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.94+1377delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342357 | |||||
chr3:112342358
|
T | C | 29 | a0001c0001t0001g0029a0001c0001t0001g0040a0001c0001t0001g0041others(26): Show | 31 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.94+1375T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342358 | ||||||
chr3:112342360
|
T | C | 46 | a0001c0001t0001g0013a0001c0001t0001g0206a0001c0001t0001g0253others(43): Show | 55 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.94+1377T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342360 | ||||||
chr3:112342361
|
C | T | 2 | a0001c0002t0003g0199a0003c0006t0007g0138 | 2 | HG02809.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.94+1378C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342361 | ||||||
chr3:112342361
|
CT | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0033others(20): Show | 37 | HG00280.hp2 HG00621.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.94+1381delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342361 | |||||
chr3:112342362
|
T | C | 10 | a0001c0001t0001g0043a0001c0001t0001g0125a0001c0001t0001g0161others(7): Show | 11 | HG01175.hp2 HG01192.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+1379T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342362 | ||||||
chr3:112342364
|
T | C | 50 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0002t0001g0006others(47): Show | 57 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.94+1381T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342364 | ||||||
chr3:112342365
|
CT | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0032others(10): Show | 22 | HG00323.hp1 HG01175.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.94+1385delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342365 | |||||
chr3:112342366
|
T | C | 5 | a0001c0001t0001g0163a0001c0001t0003g0024a0001c0001t0008g0136others(2): Show | 7 | HG01175.hp2 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1383T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342366 | ||||||
chr3:112342368
|
T | C | 50 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0018others(47): Show | 56 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.94+1385T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342368 | ||||||
chr3:112342369
|
C | T | 2 | a0003c0005t0003g0133a0003c0005t0003g0134 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.94+1386C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342369 | ||||||
chr3:112342369
|
CT | C | 11 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0205others(8): Show | 13 | HG00140.hp1 HG00639.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+1389delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342369 | |||||
chr3:112342370
|
T | C | 2 | a0001c0001t0008g0136a0001c0001t0011g0167 | 2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.94+1387T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342370 | ||||||
chr3:112342372
|
T | C | 46 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0018others(43): Show | 52 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.94+1389T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342372 | ||||||
chr3:112342373
|
CT | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0218others(1): Show | 9 | HG00438.hp1 NA18952.hp2 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+1393delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342373 | |||||
chr3:112342374
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.94+1391T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342374 | ||||||
chr3:112342376
|
T | C | 29 | a0001c0002t0001g0006a0001c0002t0001g0050a0001c0002t0001g0052others(26): Show | 31 | HG00558.hp2 HG01106.hp2 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.94+1393T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342376 | ||||||
chr3:112342377
|
C | T | 2 | a0003c0005t0010g0127a0003c0005t0010g0128 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.94+1394C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342377 | ||||||
chr3:112342378
|
T | A | 1 | a0001c0002t0001g0102 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.94+1395T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342378 | ||||||
chr3:112342380
|
T | C | 18 | a0001c0002t0001g0050a0001c0002t0001g0074a0001c0002t0001g0075others(15): Show | 18 | HG01106.hp2 HG01928.hp2 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+1397T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342380 | ||||||
chr3:112342381
|
CTTTCTTT others(6): Show |
C | 1 | a0003c0005t0003g0021 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.94+1401_94+1413del others(13): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342381 | |||||
chr3:112342382
|
TTTCTTTC others(40): Show |
T | 1 | a0001c0002t0001g0269 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94+1404_94+1450del others(47): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342382 | |||||
chr3:112342384
|
T | C | 5 | a0001c0002t0001g0074a0001c0002t0001g0119a0001c0002t0002g0069others(2): Show | 5 | HG01928.hp2 HG02451.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+1401T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342384 | ||||||
chr3:112342388
|
T | C | 1 | a0001c0002t0002g0069 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.94+1405T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342388 | ||||||
chr3:112342393
|
CT | C | 3 | a0002c0003t0001g0288a0003c0005t0003g0133a0003c0005t0003g0134 | 3 | HG02886.hp1 HG03486.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.94+1413delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342393 | |||||
chr3:112342398
|
TTTCTTTC others(24): Show |
T | 3 | a0002c0003t0001g0280a0002c0003t0001g0316a0002c0003t0001g0317 | 3 | HG01261.hp2 HG04228.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.94+1420_94+1450del others(31): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342398 | |||||
chr3:112342402
|
TTTCTTTC others(20): Show |
T | 6 | a0002c0003t0001g0281a0002c0003t0001g0282a0002c0003t0001g0318others(3): Show | 6 | HG00544.hp2 HG01256.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+1424_94+1450del others(27): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342402 | |||||
chr3:112342406
|
TTTCTTTC others(16): Show |
T | 9 | a0001c0002t0001g0066a0001c0002t0020g0182a0002c0003t0001g0039others(6): Show | 10 | HG01106.hp1 HG01516.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+1428_94+1450del others(23): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342406 | |||||
chr3:112342410
|
TTTCTTTC others(12): Show |
T | 7 | a0002c0003t0001g0038a0002c0003t0001g0268a0002c0003t0001g0283others(4): Show | 7 | HG01123.hp2 HG01934.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1432_94+1450del others(19): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342410 | |||||
chr3:112342414
|
TTTCTTTC others(8): Show |
T | 3 | a0002c0003t0001g0284a0002c0003t0001g0308a0002c0003t0001g0309 | 3 | HG00597.hp2 HG00733.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.94+1436_94+1450del others(15): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342414 | |||||
chr3:112342418
|
TTTCTTTC others(4): Show |
T | 7 | a0002c0003t0001g0292a0002c0003t0001g0310a0002c0003t0001g0311others(4): Show | 7 | HG00558.hp1 HG03239.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1440_94+1450del others(11): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342418 | |||||
chr3:112342422
|
TTTCTTTC | T | 3 | a0002c0003t0001g0312a0002c0003t0001g0313a0002c0003t0001g0327 | 3 | HG03710.hp1 HG03927.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.94+1444_94+1450del others(7): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342422 | |||||
chr3:112342426
|
TTTC | T | 29 | a0001c0001t0024g0155a0001c0002t0001g0049a0001c0002t0001g0073others(26): Show | 30 | HG00597.hp1 HG01192.hp1 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.94+1448_94+1450del others(3): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342426 | |||||
chr3:112342427
|
T | C | 2 | a0001c0002t0001g0183a0001c0002t0001g0196 | 2 | HG03516.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.94+1444T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342427 | ||||||
chr3:112342428
|
T | C | 1 | a0001c0002t0001g0116 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.94+1445T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342428 | ||||||
chr3:112342429
|
C | T | 1 | a0001c0002t0001g0116 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.94+1446C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342429 | ||||||
chr3:112342429
|
CT | C | 5 | a0001c0001t0001g0224a0001c0001t0001g0231a0001c0002t0001g0183others(2): Show | 5 | HG02622.hp2 HG03516.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+1448delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342429 | |||||
chr3:112342430
|
T | C | 67 | a0001c0001t0024g0155a0001c0002t0001g0049a0001c0002t0001g0066others(64): Show | 69 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.94+1447T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342430 | ||||||
chr3:112342430
|
T | TC | 90 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(87): Show | 97 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.94+1447_94+1448ins others(1): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342430 | ||||||
chr3:112342439
|
T | TC | 3 | a0001c0001t0001g0125a0001c0001t0001g0217a0003c0004t0001g0143 | 3 | HG03130.hp1 NA18906.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.94+1456_94+1457ins others(1): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342439 | ||||||
chr3:112342661
|
C | G | 161 | a0001c0001t0024g0155a0001c0002t0001g0006a0001c0002t0001g0007others(158): Show | 170 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.94+1678C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342661 | ||||||
chr3:112342675
|
G | A | 1 | a0002c0003t0001g0281 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.94+1692G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342675 | ||||||
chr3:112342703
|
G | A | 6 | a0001c0002t0003g0199a0003c0005t0003g0021a0003c0005t0003g0133others(3): Show | 7 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1720G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342703 | ||||||
chr3:112342740
|
T | C | 53 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(50): Show | 60 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.94+1757T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342740 | ||||||
chr3:112342790
|
T | A | 4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+1807T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342790 | ||||||
chr3:112342866
|
C | T | 4 | a0001c0002t0001g0006a0001c0002t0001g0117a0003c0005t0010g0127others(1): Show | 6 | HG02056.hp1 HG02080.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+1883C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342866 | ||||||
chr3:112342884
|
G | A | 161 | a0001c0001t0024g0155a0001c0002t0001g0006a0001c0002t0001g0007others(158): Show | 170 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.94+1901G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342884 | ||||||
chr3:112342926
|
G | C | 75 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(72): Show | 82 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.94+1943G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342926 | ||||||
chr3:112342991
|
C | CTGTG | 4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1962_95-1959dup others(4): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr3 | 112342991 | |||||
chr3:112342992
|
T | C | 2 | a0001c0002t0001g0067a0001c0002t0001g0068 | 2 | NA18747.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.95-1970T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112342992 | ||||||
chr3:112343192
|
C | G | 1 | a0001c0001t0002g0187 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.95-1770C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343192 | ||||||
chr3:112343194
|
C | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(89): Show | 128 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.95-1768C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343194 | ||||||
chr3:112343336
|
C | T | 2 | a0002c0003t0005g0326a0002c0003t0005g0330 | 2 | NA18968.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.95-1626C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343336 | ||||||
chr3:112343377
|
C | G | 72 | a0002c0003t0001g0038a0002c0003t0001g0039a0002c0003t0001g0191others(69): Show | 73 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.95-1585C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343377 | ||||||
chr3:112343440
|
A | G | 4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1522A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343440 | ||||||
chr3:112343455
|
C | T | 7 | a0001c0001t0025g0126a0001c0002t0003g0199a0003c0005t0003g0021others(4): Show | 8 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-1507C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343455 | ||||||
chr3:112343460
|
C | T | 75 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(72): Show | 82 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.95-1502C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343460 | ||||||
chr3:112343473
|
T | C | 1 | a0002c0003t0001g0292 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.95-1489T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343473 | ||||||
chr3:112343602
|
T | C | 88 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(85): Show | 96 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.95-1360T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343602 | ||||||
chr3:112343605
|
T | C | 1 | a0002c0003t0001g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.95-1357T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343605 | ||||||
chr3:112343684
|
T | C | 2 | a0001c0001t0001g0232a0001c0001t0024g0155 | 2 | HG03704.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.95-1278T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343684 | ||||||
chr3:112343881
|
C | T | 1 | a0003c0004t0001g0147 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.95-1081C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343881 | ||||||
chr3:112343989
|
T | C | 2 | a0001c0002t0001g0129a0001c0002t0001g0269 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.95-973T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112343989 | ||||||
chr3:112344073
|
C | T | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 129 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.95-889C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344073 | ||||||
chr3:112344207
|
T | C | 2 | a0001c0002t0001g0129a0001c0002t0001g0269 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.95-755T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344207 | ||||||
chr3:112344342
|
A | T | 2 | a0002c0003t0001g0268a0002c0003t0001g0323 | 2 | HG01123.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.95-620A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344342 | ||||||
chr3:112344349
|
T | G | 1 | a0001c0001t0001g0336 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.95-613T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344349 | ||||||
chr3:112344403
|
C | T | 72 | a0001c0001t0024g0155a0002c0003t0001g0038a0002c0003t0001g0039others(69): Show | 73 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.95-559C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344403 | ||||||
chr3:112344424
|
A | C | 40 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0019others(37): Show | 45 | HG01255.hp1 HG01358.hp1 HG01496.hp2 others(42): Show |
intron_variant | MODIFIER | c.95-538A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344424 | ||||||
chr3:112344482
|
T | C | 1 | a0003c0004t0002g0057 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.95-480T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344482 | ||||||
chr3:112344638
|
T | C | 75 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(72): Show | 82 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.95-324T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344638 | ||||||
chr3:112344667
|
A | C | 4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-295A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344667 | ||||||
chr3:112344667
|
A | G | 2 | a0001c0002t0001g0094a0001c0002t0001g0095 | 2 | HG03688.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.95-295A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344667 | ||||||
chr3:112344816
|
C | T | 7 | a0001c0002t0003g0199a0002c0003t0001g0325a0003c0005t0003g0021others(4): Show | 8 | HG00558.hp1 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-146C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344816 | ||||||
chr3:112344858
|
T | C | 84 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(81): Show | 92 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.95-104T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344858 | ||||||
chr3:112344907
|
A | G | 1 | a0003c0004t0003g0270 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.95-55A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344907 | ||||||
chr3:112344918
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.95-44G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 2/5 | chr3 | 112344918 | ||||||
chr3:112345352
|
T | C | 3 | a0001c0001t0001g0205a0001c0001t0001g0208a0001c0001t0001g0233 | 3 | HG02486.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421+64T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345352 | ||||||
chr3:112345401
|
A | G | 4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+113A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345401 | ||||||
chr3:112345416
|
T | A | 88 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(85): Show | 96 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.421+128T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345416 | ||||||
chr3:112345419
|
T | C | 70 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(67): Show | 77 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.421+131T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345419 | ||||||
chr3:112345479
|
G | T | 3 | a0001c0002t0002g0046a0001c0002t0002g0265a0001c0002t0023g0047 | 3 | HG02886.hp2 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.421+191G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345479 | ||||||
chr3:112345488
|
A | G | 4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+200A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345488 | ||||||
chr3:112345606
|
C | A | 1 | a0001c0001t0001g0225 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.421+318C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345606 | ||||||
chr3:112345629
|
C | T | 4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+341C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345629 | ||||||
chr3:112345774
|
T | G | 1 | a0003c0004t0002g0059 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.421+486T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345774 | ||||||
chr3:112345812
|
G | A | 1 | a0002c0003t0001g0316 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.421+524G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345812 | ||||||
chr3:112345904
|
A | G | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 407 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(404): Show |
intron_variant | MODIFIER | c.421+616A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345904 | ||||||
chr3:112345939
|
G | T | 4 | a0001c0002t0001g0070a0001c0002t0001g0080a0001c0002t0001g0087others(1): Show | 4 | NA18939.hp1 NA18942.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+651G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345939 | ||||||
chr3:112345983
|
C | T | 84 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(81): Show | 92 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.421+695C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112345983 | ||||||
chr3:112346032
|
T | C | 84 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(81): Show | 92 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.421+744T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346032 | ||||||
chr3:112346065
|
G | T | 4 | a0001c0001t0001g0122a0001c0001t0002g0120a0001c0001t0002g0121others(1): Show | 4 | HG02280.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+777G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346065 | ||||||
chr3:112346119
|
G | GCCAAAAG others(356): Show |
1 | a0001c0001t0002g0237 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.421+849_421+850ins others(363): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr3 | 112346119 | |||||
chr3:112346181
|
T | C | 326 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(323): Show | 380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.421+893T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346181 | ||||||
chr3:112346390
|
C | T | 1 | a0002c0003t0002g0273 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.421+1102C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346390 | ||||||
chr3:112346491
|
C | T | 1 | a0001c0001t0018g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.422-1067C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346491 | ||||||
chr3:112346567
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.422-991C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346567 | ||||||
chr3:112346594
|
T | C | 1 | a0002c0003t0001g0321 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.422-964T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346594 | ||||||
chr3:112346890
|
G | T | 326 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(323): Show | 380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.422-668G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346890 | ||||||
chr3:112346971
|
C | T | 9 | a0001c0002t0001g0129a0001c0002t0001g0269a0001c0002t0003g0199others(6): Show | 10 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.422-587C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346971 | ||||||
chr3:112346988
|
G | A | 3 | a0001c0002t0001g0183a0001c0002t0003g0118a0001c0002t0022g0245 | 3 | HG02451.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.422-570G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112346988 | ||||||
chr3:112347042
|
G | A | 1 | a0001c0002t0020g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.422-516G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112347042 | ||||||
chr3:112347263
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.422-295A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112347263 | ||||||
chr3:112347294
|
C | T | 73 | a0001c0001t0024g0155a0002c0003t0001g0038a0002c0003t0001g0039others(70): Show | 74 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.422-264C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112347294 | ||||||
chr3:112347513
|
C | T | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(38): Show | 48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.422-45C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 3/5 | chr3 | 112347513 | ||||||
chr3:112347975
|
C | A | 5 | a0001c0002t0001g0070a0001c0002t0001g0080a0001c0002t0001g0087others(2): Show | 5 | HG06807.hp2 NA18939.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.694+145C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112347975 | ||||||
chr3:112348239
|
G | T | 1 | a0001c0002t0020g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.694+409G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348239 | ||||||
chr3:112348394
|
C | T | 77 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(74): Show | 84 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.694+564C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348394 | ||||||
chr3:112348591
|
C | G | 87 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(84): Show | 95 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.694+761C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348591 | ||||||
chr3:112348599
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.694+769C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348599 | ||||||
chr3:112348738
|
T | C | 6 | a0001c0002t0003g0199a0003c0005t0003g0021a0003c0005t0003g0133others(3): Show | 7 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.694+908T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348738 | ||||||
chr3:112348768
|
G | A | 12 | a0001c0002t0001g0017a0001c0002t0001g0052a0001c0002t0001g0066others(9): Show | 13 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.694+938G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348768 | ||||||
chr3:112348849
|
GGAA | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 129 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.695-862_695-860del others(3): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348849 | ||||||
chr3:112348866
|
A | G | 1 | a0001c0002t0002g0105 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.695-846A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348866 | ||||||
chr3:112348877
|
C | CT | 92 | a0001c0001t0006g0263a0001c0002t0001g0006a0001c0002t0001g0007others(89): Show | 100 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.695-825dupT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 112348877 | |||||
chr3:112348971
|
CA | C | 78 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(75): Show | 85 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.695-735delA | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 112348971 | |||||
chr3:112348977
|
A | T | 78 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(75): Show | 85 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.695-735A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112348977 | ||||||
chr3:112349015
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.695-697A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349015 | ||||||
chr3:112349016
|
T | A | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.695-696T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349016 | ||||||
chr3:112349017
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.695-695A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349017 | ||||||
chr3:112349049
|
G | A | 1 | a0001c0002t0020g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.695-663G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349049 | ||||||
chr3:112349076
|
A | G | 1 | a0002c0003t0001g0292 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.695-636A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349076 | ||||||
chr3:112349089
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.695-623A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349089 | ||||||
chr3:112349090
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.695-622G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349090 | ||||||
chr3:112349217
|
C | A | 91 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(88): Show | 99 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.695-495C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349217 | ||||||
chr3:112349277
|
T | G | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.695-435T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349277 | ||||||
chr3:112349298
|
C | T | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(38): Show | 48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.695-414C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349298 | ||||||
chr3:112349407
|
T | C | 2 | a0001c0001t0001g0262a0001c0001t0001g0266 | 2 | HG00735.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.695-305T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349407 | ||||||
chr3:112349439
|
C | A | 1 | a0001c0001t0018g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695-273C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349439 | ||||||
chr3:112349501
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0179 | 3 | HG00642.hp2 HG02257.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.695-211G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349501 | ||||||
chr3:112349509
|
T | G | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.695-203T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349509 | ||||||
chr3:112349572
|
T | C | 1 | a0001c0001t0001g0242 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.695-140T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349572 | ||||||
chr3:112349593
|
C | T | 87 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(84): Show | 95 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.695-119C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349593 | ||||||
chr3:112349620
|
A | C | 1 | a0001c0001t0001g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.695-92A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349620 | ||||||
chr3:112349647
|
T | TCTATTGC others(7): Show |
87 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(84): Show | 95 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.695-63_695-62insAT others(12): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr3 | 112349647 | |||||
chr3:112349656
|
C | T | 3 | a0003c0004t0001g0023a0003c0004t0001g0149a0003c0004t0001g0151 | 4 | HG01167.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-56C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349656 | ||||||
chr3:112349670
|
C | T | 78 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0017others(75): Show | 85 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.695-42C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 4/5 | chr3 | 112349670 | ||||||
chr3:112349828
|
T | A | 4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+9T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112349828 | ||||||
chr3:112349880
|
T | C | 6 | a0001c0002t0003g0199a0003c0005t0003g0021a0003c0005t0003g0133others(3): Show | 7 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+61T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112349880 | ||||||
chr3:112349928
|
T | C | 1 | a0001c0002t0002g0279 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.802+109T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112349928 | ||||||
chr3:112349976
|
G | A | 3 | a0001c0002t0001g0183a0001c0002t0003g0118a0001c0002t0022g0245 | 3 | HG02451.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.802+157G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112349976 | ||||||
chr3:112350108
|
C | T | 1 | a0001c0002t0001g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.802+289C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112350108 | ||||||
chr3:112350545
|
T | C | 144 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(141): Show | 159 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.802+726T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112350545 | ||||||
chr3:112350708
|
G | A | 1 | a0001c0001t0003g0024 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.802+889G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112350708 | ||||||
chr3:112350728
|
G | T | 1 | a0001c0002t0002g0279 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.802+909G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112350728 | ||||||
chr3:112350908
|
T | C | 71 | a0002c0003t0001g0038a0002c0003t0001g0039a0002c0003t0001g0191others(68): Show | 72 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.802+1089T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112350908 | ||||||
chr3:112350918
|
C | A | 310 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(307): Show | 363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.802+1099C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112350918 | ||||||
chr3:112351037
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.802+1218C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351037 | ||||||
chr3:112351076
|
CTGTT | C | 4 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0250others(1): Show | 4 | HG00140.hp1 HG00280.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+1260_802+1263d others(6): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112351076 | |||||
chr3:112351111
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.802+1292T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351111 | ||||||
chr3:112351113
|
C | A | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.802+1294C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351113 | ||||||
chr3:112351115
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.802+1296A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351115 | ||||||
chr3:112351242
|
A | G | 4 | a0001c0001t0001g0220a0001c0001t0001g0249a0001c0001t0009g0222others(1): Show | 4 | NA18954.hp1 NA18981.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+1423A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351242 | ||||||
chr3:112351613
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.802+1794G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351613 | ||||||
chr3:112351640
|
G | A | 17 | a0001c0001t0001g0137a0001c0001t0001g0262a0001c0001t0001g0266others(14): Show | 17 | HG00544.hp1 HG00735.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+1821G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351640 | ||||||
chr3:112351677
|
G | GAATGTTC others(14): Show |
17 | a0001c0001t0001g0137a0001c0001t0001g0262a0001c0001t0001g0266others(14): Show | 17 | HG00544.hp1 HG00735.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+1862_802+1863i others(23): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112351677 | |||||
chr3:112351729
|
T | A | 58 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(55): Show | 65 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.802+1910T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351729 | ||||||
chr3:112351887
|
G | A | 3 | a0001c0001t0002g0184a0001c0001t0002g0186a0001c0001t0002g0187 | 3 | NA18939.hp2 NA18941.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.802+2068G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351887 | ||||||
chr3:112351911
|
C | T | 1 | a0001c0002t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.802+2092C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351911 | ||||||
chr3:112351947
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.802+2128C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112351947 | ||||||
chr3:112352089
|
C | T | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 407 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(404): Show |
intron_variant | MODIFIER | c.802+2270C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352089 | ||||||
chr3:112352101
|
T | C | 2 | a0001c0002t0001g0129a0001c0002t0001g0269 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.802+2282T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352101 | ||||||
chr3:112352131
|
T | C | 1 | a0001c0002t0002g0279 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.802+2312T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352131 | ||||||
chr3:112352221
|
C | A | 2 | a0001c0002t0002g0046a0001c0002t0023g0047 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.802+2402C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352221 | ||||||
chr3:112352348
|
C | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0269a0001c0002t0020g0182 | 3 | HG02109.hp2 HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.802+2529C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352348 | ||||||
chr3:112352354
|
A | G | 1 | a0001c0001t0024g0155 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.802+2535A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352354 | ||||||
chr3:112352382
|
C | T | 1 | a0001c0002t0002g0279 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.802+2563C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352382 | ||||||
chr3:112352435
|
A | G | 41 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(38): Show | 48 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.802+2616A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352435 | ||||||
chr3:112352451
|
C | T | 5 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0002g0184others(2): Show | 5 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.802+2632C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352451 | ||||||
chr3:112352540
|
TGA | T | 81 | a0001c0001t0001g0033a0001c0001t0003g0024a0001c0002t0003g0199others(78): Show | 85 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.802+2747_802+2748d others(4): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112352540 | |||||
chr3:112352540
|
TGAGA | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 210 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.802+2745_802+2748d others(6): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112352540 | |||||
chr3:112352540
|
TGAGAGA | T | 10 | a0001c0001t0001g0137a0001c0001t0001g0176a0001c0001t0001g0262others(7): Show | 10 | HG00735.hp2 HG01081.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.802+2743_802+2748d others(8): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112352540 | |||||
chr3:112352540
|
TGAGAGAG others(1): Show |
T | 48 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(45): Show | 55 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.802+2741_802+2748d others(10): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112352540 | |||||
chr3:112352564
|
AGAGT | A | 4 | a0001c0001t0001g0122a0001c0001t0002g0120a0001c0001t0002g0121others(1): Show | 4 | HG02280.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+2747_802+2750d others(6): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112352564 | |||||
chr3:112352566
|
A | T | 49 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(46): Show | 56 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.802+2747A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352566 | ||||||
chr3:112352629
|
T | C | 3 | a0001c0002t0001g0246a0001c0002t0003g0090a0001c0002t0021g0101 | 3 | HG02258.hp2 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.802+2810T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352629 | ||||||
chr3:112352825
|
G | A | 5 | a0001c0002t0001g0081a0001c0002t0001g0094a0001c0002t0001g0095others(2): Show | 5 | HG02818.hp1 HG03471.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.802+3006G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352825 | ||||||
chr3:112352837
|
C | T | 1 | a0001c0001t0025g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.802+3018C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352837 | ||||||
chr3:112352863
|
TATAATGC others(8): Show |
T | 1 | a0001c0002t0001g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.802+3047_802+3061d others(17): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112352863 | |||||
chr3:112352884
|
G | A | 6 | a0003c0004t0001g0061a0003c0004t0002g0053a0003c0004t0002g0054others(3): Show | 6 | HG02056.hp2 HG02129.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+3065G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352884 | ||||||
chr3:112352960
|
C | A | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.802+3141C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112352960 | ||||||
chr3:112353086
|
C | T | 1 | a0001c0002t0001g0086 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.802+3267C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353086 | ||||||
chr3:112353087
|
G | A | 58 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(55): Show | 65 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.802+3268G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353087 | ||||||
chr3:112353184
|
A | G | 4 | a0001c0001t0001g0122a0001c0001t0002g0120a0001c0001t0002g0121others(1): Show | 4 | HG02280.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+3365A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353184 | ||||||
chr3:112353249
|
T | A | 1 | a0001c0001t0001g0201 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.802+3430T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353249 | ||||||
chr3:112353309
|
G | GTTTGC | 47 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(44): Show | 54 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.802+3500_802+3504d others(7): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112353309 | |||||
chr3:112353324
|
G | C | 58 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(55): Show | 65 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.802+3505G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353324 | ||||||
chr3:112353572
|
A | C | 4 | a0001c0001t0001g0156a0001c0001t0004g0157a0001c0001t0004g0158others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+3753A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353572 | ||||||
chr3:112353613
|
CA | C | 3 | a0001c0002t0001g0183a0001c0002t0003g0118a0001c0002t0022g0245 | 3 | HG02451.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.802+3796delA | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112353613 | |||||
chr3:112353621
|
G | A | 1 | a0003c0004t0002g0130 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.802+3802G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353621 | ||||||
chr3:112353753
|
G | A | 3 | a0002c0003t0001g0300a0002c0003t0001g0303a0002c0003t0001g0312 | 3 | NA18975.hp1 NA18981.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.802+3934G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353753 | ||||||
chr3:112353779
|
C | T | 1 | a0002c0003t0001g0281 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.802+3960C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353779 | ||||||
chr3:112353825
|
T | C | 3 | a0001c0001t0004g0157a0001c0001t0004g0158a0001c0001t0004g0159 | 3 | HG02280.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.802+4006T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353825 | ||||||
chr3:112353831
|
C | T | 2 | a0001c0002t0003g0199a0003c0005t0003g0133 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.802+4012C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353831 | ||||||
chr3:112353980
|
A | G | 4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+4161A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353980 | ||||||
chr3:112353986
|
G | A | 120 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0028others(117): Show | 128 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.802+4167G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353986 | ||||||
chr3:112353996
|
T | G | 1 | a0001c0001t0024g0155 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.802+4177T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112353996 | ||||||
chr3:112354146
|
C | T | 4 | a0002c0003t0001g0305a0002c0003t0001g0306a0002c0003t0001g0308others(1): Show | 4 | HG00597.hp2 NA18963.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+4327C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354146 | ||||||
chr3:112354182
|
G | A | 1 | a0002c0003t0001g0339 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.802+4363G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354182 | ||||||
chr3:112354286
|
T | C | 89 | a0001c0001t0001g0028a0002c0003t0001g0038a0002c0003t0001g0039others(86): Show | 92 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.802+4467T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354286 | ||||||
chr3:112354520
|
C | A | 1 | a0001c0002t0020g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.802+4701C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354520 | ||||||
chr3:112354736
|
A | C | 1 | a0001c0001t0003g0024 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.802+4917A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354736 | ||||||
chr3:112354809
|
G | A | 2 | a0002c0003t0001g0305a0002c0003t0001g0311 | 2 | NA18983.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.802+4990G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354809 | ||||||
chr3:112354827
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0207a0001c0001t0001g0215 | 4 | HG01243.hp1 HG03669.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+5008C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354827 | ||||||
chr3:112354989
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.802+5170C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112354989 | ||||||
chr3:112355031
|
A | G | 1 | a0002c0003t0002g0273 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.802+5212A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355031 | ||||||
chr3:112355040
|
C | A | 5 | a0001c0002t0001g0020a0001c0002t0001g0082a0001c0002t0001g0083others(2): Show | 6 | HG02132.hp2 NA18960.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+5221C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355040 | ||||||
chr3:112355239
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0228 | 2 | HG01975.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.802+5420C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355239 | ||||||
chr3:112355243
|
A | T | 1 | a0001c0001t0001g0202 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.802+5424A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355243 | ||||||
chr3:112355300
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(139): Show | 184 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.802+5481G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355300 | ||||||
chr3:112355383
|
C | G | 2 | a0003c0004t0001g0141a0003c0004t0001g0143 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.802+5564C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355383 | ||||||
chr3:112355484
|
C | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 186 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.802+5665C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355484 | ||||||
chr3:112355732
|
T | A | 2 | a0001c0002t0001g0129a0001c0002t0001g0269 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.803-5811T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355732 | ||||||
chr3:112355761
|
G | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 186 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.803-5782G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355761 | ||||||
chr3:112355862
|
A | G | 1 | a0001c0001t0001g0337 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.803-5681A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355862 | ||||||
chr3:112355874
|
T | A | 5 | a0001c0001t0001g0194a0001c0001t0001g0203a0001c0001t0001g0209others(2): Show | 5 | HG00408.hp2 HG00673.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-5669T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355874 | ||||||
chr3:112355874
|
T | G | 2 | a0001c0002t0001g0129a0001c0002t0001g0269 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.803-5669T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112355874 | ||||||
chr3:112355899
|
CAATTT | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 129 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.803-5638_803-5634d others(7): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112355899 | |||||
chr3:112356091
|
A | G | 4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-5452A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356091 | ||||||
chr3:112356130
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 131 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.803-5413A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356130 | ||||||
chr3:112356304
|
T | C | 1 | a0001c0001t0024g0155 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.803-5239T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356304 | ||||||
chr3:112356355
|
AT | A | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.803-5181delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112356355 | |||||
chr3:112356357
|
T | A | 1 | a0001c0001t0001g0249 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.803-5186T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356357 | ||||||
chr3:112356551
|
C | T | 1 | a0001c0002t0001g0079 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.803-4992C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356551 | ||||||
chr3:112356619
|
T | G | 1 | a0001c0002t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.803-4924T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356619 | ||||||
chr3:112356749
|
T | A | 1 | a0001c0002t0021g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.803-4794T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356749 | ||||||
chr3:112356807
|
T | C | 2 | a0002c0003t0001g0305a0002c0003t0001g0311 | 2 | NA18983.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.803-4736T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356807 | ||||||
chr3:112356935
|
A | G | 1 | a0001c0002t0016g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.803-4608A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356935 | ||||||
chr3:112356945
|
G | A | 1 | a0001c0002t0001g0072 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.803-4598G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112356945 | ||||||
chr3:112357141
|
G | A | 2 | a0001c0002t0001g0129a0001c0002t0001g0269 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.803-4402G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357141 | ||||||
chr3:112357192
|
C | T | 1 | a0001c0001t0025g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.803-4351C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357192 | ||||||
chr3:112357239
|
G | C | 81 | a0001c0001t0001g0028a0001c0001t0001g0174a0001c0001t0001g0175others(78): Show | 83 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.803-4304G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357239 | ||||||
chr3:112357253
|
T | G | 5 | a0001c0002t0001g0020a0001c0002t0001g0082a0001c0002t0001g0083others(2): Show | 6 | HG02132.hp2 NA18960.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-4290T>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357253 | ||||||
chr3:112357258
|
C | CA | 80 | a0001c0001t0001g0028a0001c0001t0001g0045a0001c0001t0001g0174others(77): Show | 83 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.803-4269dupA | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112357258 | |||||
chr3:112357258
|
C | CAA | 15 | a0001c0001t0001g0262a0001c0001t0001g0266a0001c0001t0003g0024others(12): Show | 16 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.803-4270_803-4269d others(4): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112357258 | |||||
chr3:112357271
|
A | AAAAG | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(84): Show | 122 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.803-4252_803-4249d others(6): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112357271 | |||||
chr3:112357271
|
A | AG | 6 | a0001c0002t0003g0199a0003c0005t0003g0021a0003c0005t0003g0133others(3): Show | 7 | HG02257.hp1 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-4272_803-4271i others(3): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357271 | ||||||
chr3:112357275
|
G | A | 81 | a0001c0001t0001g0028a0001c0001t0001g0174a0001c0001t0001g0175others(78): Show | 83 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.803-4268G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357275 | ||||||
chr3:112357295
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.803-4248A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357295 | ||||||
chr3:112357373
|
C | G | 1 | a0002c0003t0001g0334 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.803-4170C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357373 | ||||||
chr3:112357381
|
T | C | 1 | a0001c0001t0001g0217 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.803-4162T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357381 | ||||||
chr3:112357456
|
C | T | 3 | a0001c0001t0024g0155a0001c0002t0001g0129a0001c0002t0001g0269 | 3 | HG02109.hp2 HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.803-4087C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357456 | ||||||
chr3:112357697
|
A | G | 1 | a0001c0001t0025g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.803-3846A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357697 | ||||||
chr3:112357720
|
G | A | 1 | a0001c0002t0001g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.803-3823G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357720 | ||||||
chr3:112357751
|
T | C | 1 | a0001c0002t0002g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.803-3792T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357751 | ||||||
chr3:112357754
|
G | A | 1 | a0002c0003t0001g0302 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.803-3789G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357754 | ||||||
chr3:112357786
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.803-3757A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357786 | ||||||
chr3:112357798
|
G | A | 2 | a0001c0001t0001g0226a0003c0004t0001g0154 | 2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.803-3745G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357798 | ||||||
chr3:112357924
|
A | G | 5 | a0001c0002t0001g0070a0001c0002t0001g0080a0001c0002t0001g0087others(2): Show | 5 | HG06807.hp2 NA18939.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-3619A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357924 | ||||||
chr3:112357951
|
G | A | 1 | a0003c0005t0010g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.803-3592G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112357951 | ||||||
chr3:112358026
|
G | C | 1 | a0003c0006t0007g0139 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.803-3517G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358026 | ||||||
chr3:112358155
|
T | A | 4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-3388T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358155 | ||||||
chr3:112358219
|
G | A | 1 | a0001c0002t0001g0112 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.803-3324G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358219 | ||||||
chr3:112358262
|
G | A | 137 | a0001c0001t0001g0028a0001c0001t0001g0174a0001c0001t0001g0175others(134): Show | 146 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.803-3281G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358262 | ||||||
chr3:112358366
|
G | A | 7 | a0001c0002t0001g0183a0001c0002t0002g0046a0001c0002t0002g0265others(4): Show | 7 | HG02451.hp2 HG02886.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-3177G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358366 | ||||||
chr3:112358367
|
TG | T | 138 | a0001c0001t0001g0028a0001c0001t0001g0174a0001c0001t0001g0175others(135): Show | 148 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.803-3172delG | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112358367 | |||||
chr3:112358418
|
C | A | 7 | a0001c0001t0001g0262a0001c0001t0001g0266a0001c0001t0006g0258others(4): Show | 7 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-3125C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358418 | ||||||
chr3:112358428
|
AATGAACT others(12): Show |
A | 1 | a0002c0003t0001g0271 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.803-3098_803-3080d others(21): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112358428 | |||||
chr3:112358487
|
AG | A | 50 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(47): Show | 62 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.803-3055delG | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358487 | ||||||
chr3:112358493
|
A | T | 6 | a0001c0001t0001g0262a0001c0001t0001g0266a0001c0001t0006g0258others(3): Show | 6 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-3050A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358493 | ||||||
chr3:112358610
|
T | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(77): Show | 107 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.803-2933T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358610 | ||||||
chr3:112358649
|
C | T | 1 | a0001c0002t0001g0100 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.803-2894C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358649 | ||||||
chr3:112358667
|
G | A | 3 | a0001c0001t0024g0155a0003c0005t0010g0127a0003c0005t0010g0128 | 3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.803-2876G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358667 | ||||||
chr3:112358691
|
C | G | 53 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(50): Show | 65 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.803-2852C>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358691 | ||||||
chr3:112358741
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.803-2802T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358741 | ||||||
chr3:112358837
|
C | T | 52 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(49): Show | 64 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.803-2706C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358837 | ||||||
chr3:112358857
|
C | A | 53 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(50): Show | 65 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.803-2686C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358857 | ||||||
chr3:112358883
|
C | A | 53 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(50): Show | 65 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.803-2660C>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112358883 | ||||||
chr3:112358918
|
GGAAAGAA others(7): Show |
G | 36 | a0001c0001t0001g0122a0001c0001t0001g0137a0001c0001t0002g0120others(33): Show | 37 | HG00438.hp2 HG00609.hp2 HG02056.hp2 others(34): Show |
intron_variant | MODIFIER | c.803-2610_803-2597d others(16): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112358918 | |||||
chr3:112358931
|
G | GAGAAAGA others(1): Show |
47 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(44): Show | 59 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.803-2608_803-2601d others(10): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112358931 | |||||
chr3:112358931
|
G | GAGAAAGA others(5): Show |
4 | a0003c0006t0007g0138a0003c0006t0007g0139a0003c0006t0007g0140others(1): Show | 4 | HG00544.hp1 HG02735.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-2601_803-2600i others(14): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112358931 | |||||
chr3:112359033
|
G | A | 51 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(48): Show | 63 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.803-2510G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359033 | ||||||
chr3:112359105
|
T | C | 8 | a0001c0001t0003g0024a0001c0002t0003g0090a0001c0002t0003g0118others(5): Show | 10 | HG02129.hp2 HG02257.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-2438T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359105 | ||||||
chr3:112359247
|
T | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(81): Show | 111 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.803-2296T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359247 | ||||||
chr3:112359287
|
A | G | 51 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(48): Show | 63 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.803-2256A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359287 | ||||||
chr3:112359310
|
C | T | 47 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(44): Show | 59 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.803-2233C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359310 | ||||||
chr3:112359375
|
G | A | 1 | a0001c0001t0017g0236 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.803-2168G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359375 | ||||||
chr3:112359517
|
A | G | 1 | a0001c0002t0001g0072 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.803-2026A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359517 | ||||||
chr3:112359609
|
T | A | 2 | a0001c0002t0001g0129a0001c0002t0001g0269 | 2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.803-1934T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359609 | ||||||
chr3:112359685
|
T | C | 2 | a0002c0003t0008g0190a0002c0003t0008g0192 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.803-1858T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359685 | ||||||
chr3:112359721
|
T | C | 47 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(44): Show | 59 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.803-1822T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359721 | ||||||
chr3:112359749
|
G | C | 2 | a0002c0003t0001g0314a0002c0003t0001g0333 | 2 | HG01952.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.803-1794G>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359749 | ||||||
chr3:112359771
|
G | T | 47 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(44): Show | 59 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.803-1772G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359771 | ||||||
chr3:112359848
|
A | T | 47 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(44): Show | 59 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.803-1695A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359848 | ||||||
chr3:112359893
|
T | A | 47 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(44): Show | 59 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.803-1650T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112359893 | ||||||
chr3:112359900
|
AGG | A | 4 | a0003c0004t0001g0009a0003c0004t0001g0010a0003c0004t0001g0150others(1): Show | 8 | HG01109.hp2 HG01123.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-1641_803-1640d others(4): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112359900 | |||||
chr3:112360061
|
C | T | 1 | a0002c0003t0001g0314 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.803-1482C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360061 | ||||||
chr3:112360099
|
A | T | 1 | a0003c0004t0002g0131 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.803-1444A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360099 | ||||||
chr3:112360170
|
A | T | 1 | a0001c0002t0001g0096 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.803-1373A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360170 | ||||||
chr3:112360185
|
G | T | 1 | a0001c0002t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.803-1358G>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360185 | ||||||
chr3:112360241
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(110): Show | 141 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.803-1302T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360241 | ||||||
chr3:112360284
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0004g0157a0001c0001t0004g0158others(1): Show | 4 | HG02280.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1259C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360284 | ||||||
chr3:112360308
|
A | C | 1 | a0001c0001t0001g0223 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.803-1235A>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360308 | ||||||
chr3:112360326
|
T | TAAAAATA others(3): Show |
65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(62): Show | 92 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.803-1212_803-1211i others(12): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112360326 | |||||
chr3:112360326
|
T | TAAAAATA others(4): Show |
2 | a0001c0001t0001g0205a0001c0001t0001g0207 | 2 | HG02486.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.803-1212_803-1211i others(13): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112360326 | |||||
chr3:112360326
|
T | TAAAAATA others(5): Show |
4 | a0001c0001t0001g0137a0001c0002t0016g0051a0003c0004t0001g0141others(1): Show | 4 | HG02895.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-1212_803-1211i others(14): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112360326 | |||||
chr3:112360331
|
A | ATAAAAAA others(5): Show |
5 | a0001c0001t0002g0120a0001c0001t0017g0236a0003c0004t0002g0016others(2): Show | 5 | HG00438.hp2 HG02572.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-1212_803-1211i others(14): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360331 | ||||||
chr3:112360331
|
A | ATAAAAAA others(7): Show |
1 | a0002c0003t0002g0276 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.803-1212_803-1211i others(16): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360331 | ||||||
chr3:112360331
|
A | ATAAAAAA others(3): Show |
10 | a0001c0001t0001g0203a0001c0001t0001g0209a0001c0001t0001g0210others(7): Show | 10 | HG00408.hp2 HG00673.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-1212_803-1211i others(12): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360331 | ||||||
chr3:112360331
|
A | ATAAAAAA others(5): Show |
24 | a0001c0001t0001g0122a0001c0001t0002g0121a0001c0001t0002g0123others(21): Show | 25 | HG00609.hp2 HG02056.hp2 HG02074.hp2 others(22): Show |
intron_variant | MODIFIER | c.803-1212_803-1211i others(14): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360331 | ||||||
chr3:112360331
|
A | ATAAAAAA others(5): Show |
2 | a0001c0001t0002g0160a0001c0002t0002g0046 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.803-1212_803-1211i others(14): Show |
CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360331 | ||||||
chr3:112360333
|
A | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0064others(63): Show | 77 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.803-1210A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360333 | ||||||
chr3:112360334
|
AT | A | 46 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(43): Show | 58 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.803-1208delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360334 | ||||||
chr3:112360335
|
T | A | 5 | a0001c0001t0001g0175a0001c0001t0001g0194a0001c0002t0001g0092others(2): Show | 5 | HG00642.hp2 HG01256.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-1208T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360335 | ||||||
chr3:112360358
|
T | C | 2 | a0001c0001t0003g0024a0001c0002t0003g0118 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.803-1185T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360358 | ||||||
chr3:112360430
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(173): Show | 218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.803-1113T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360430 | ||||||
chr3:112360436
|
A | T | 1 | a0002c0003t0001g0321 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.803-1107A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360436 | ||||||
chr3:112360521
|
A | G | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0179 | 3 | HG00642.hp2 HG02257.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.803-1022A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360521 | ||||||
chr3:112360569
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.803-974T>C | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360569 | ||||||
chr3:112360620
|
T | A | 1 | a0001c0002t0001g0094 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.803-923T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360620 | ||||||
chr3:112360777
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042 | 3 | HG00280.hp1 HG01361.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.803-766G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360777 | ||||||
chr3:112360813
|
A | T | 1 | a0001c0002t0001g0183 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.803-730A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360813 | ||||||
chr3:112360933
|
A | G | 47 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(44): Show | 59 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.803-610A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360933 | ||||||
chr3:112360950
|
C | T | 3 | a0001c0002t0001g0007a0001c0002t0001g0074a0001c0002t0001g0098 | 5 | HG01255.hp1 HG01358.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-593C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112360950 | ||||||
chr3:112361131
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.803-412A>G | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361131 | ||||||
chr3:112361149
|
G | A | 1 | a0001c0002t0002g0265 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.803-394G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361149 | ||||||
chr3:112361202
|
AT | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(138): Show | 171 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.803-330delT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112361202 | |||||
chr3:112361262
|
T | A | 1 | a0002c0003t0001g0309 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.803-281T>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361262 | ||||||
chr3:112361293
|
G | A | 1 | a0001c0002t0001g0083 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.803-250G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361293 | ||||||
chr3:112361295
|
C | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(110): Show | 141 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.803-248C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361295 | ||||||
chr3:112361311
|
A | T | 1 | a0001c0001t0001g0175 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.803-232A>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361311 | ||||||
chr3:112361314
|
G | A | 6 | a0001c0001t0001g0262a0001c0001t0001g0266a0001c0001t0006g0258others(3): Show | 6 | HG00735.hp2 HG01081.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-229G>A | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361314 | ||||||
chr3:112361368
|
C | T | 3 | a0001c0001t0024g0155a0003c0005t0010g0127a0003c0005t0010g0128 | 3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.803-175C>T | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | chr3 | 112361368 | ||||||
chr3:112361442
|
ACT | A | 3 | a0001c0001t0024g0155a0003c0005t0010g0127a0003c0005t0010g0128 | 3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.803-98_803-97delCT | CD200 | ENSG00000091972.18 | transcript | ENST00000315711.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr3 | 112361442 |