geneid | 1356 |
---|---|
ensemblid | ENSG00000047457.14 |
hgncid | 2295 |
symbol | CP |
name | ceruloplasmin |
refseq_nuc | NM_000096.4 |
refseq_prot | NP_000087.2 |
ensembl_nuc | ENST00000264613.11 |
ensembl_prot | ENSP00000264613.6 |
mane_status | MANE Select |
chr | chr3 |
start | 149172497 |
end | 149221829 |
strand | - |
ver | v1.2 |
region | chr3:149172497-149221829 |
region5000 | chr3:149167497-149226829 |
regionname0 | CP_chr3_149172497_149221829 |
regionname5000 | CP_chr3_149167497_149226829 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1065 | 298 | 43 | 53 | 149 | 13 | 39 | 117 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0002 | 1/0 | 1065 | 47 | 32 | 4 | 0 | 5 | 5 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0003 | 0/0 | 1065 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0004 | 0/0 | 1065 | 5 | 0 | 2 | 0 | 0 | 3 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0005 | 0/0 | 1065 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0006 | 0/0 | 1065 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0007 | 0/0 | 1065 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0008 | 0/0 | 1065 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0009 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0010 | 0/0 | 1065 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0011 | 0/0 | 1065 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0012 | 0/0 | 1065 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0013 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0014 | 0/0 | 1065 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0015 | 0/0 | 1065 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0016 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0017 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 3198 | 276 | 40 | 40 | 144 | 13 | 38 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0002 | 1/0 | 3198 | 41 | 28 | 2 | 0 | 5 | 5 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0003 | 0/0 | 3198 | 8 | 0 | 8 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0004 | 0/0 | 3198 | 8 | 6 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0005 | 0/0 | 3198 | 6 | 0 | 5 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0006 | 0/0 | 3198 | 4 | 4 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0007 | 0/0 | 3198 | 3 | 3 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0008 | 0/0 | 3198 | 3 | 2 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0009 | 0/0 | 3198 | 3 | 0 | 2 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0010 | 0/0 | 3198 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0011 | 0/0 | 3198 | 2 | 0 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0012 | 0/0 | 3198 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0013 | 0/0 | 3198 | 2 | 0 | 0 | 0 | 0 | 2 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0014 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0015 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0016 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0017 | 0/0 | 3198 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0018 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0019 | 0/0 | 3198 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0020 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0021 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0022 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0023 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0024 | 0/0 | 3198 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0025 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0026 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0027 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0028 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
c0029 | 0/0 | 3198 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1255 | 280 | 46 | 52 | 126 | 13 | 41 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
t0002 | 0/0 | 1255 | 53 | 23 | 5 | 20 | 1 | 4 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
t0003 | 0/0 | 1256 | 15 | 12 | 3 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
t0004 | 0/0 | 1255 | 7 | 0 | 1 | 4 | 1 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
t0005 | 0/0 | 1256 | 4 | 4 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
t0006 | 0/0 | 1256 | 4 | 4 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
t0007 | 0/0 | 1255 | 4 | 0 | 2 | 0 | 0 | 2 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
t0008 | 0/0 | 1255 | 3 | 0 | 1 | 0 | 2 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
t0009 | 0/0 | 1256 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
t0010 | 0/0 | 1255 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
t0011 | 0/0 | 1255 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
t0012 | 0/0 | 1255 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0006 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0011 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0024 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3198 | 276 | 40 | 40 | 144 | 13 | 38 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0003 | 0/0 | 3198 | 8 | 0 | 8 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0005 | 0/0 | 3198 | 6 | 0 | 5 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0010 | 0/0 | 3198 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0014 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0018 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0019 | 0/0 | 3198 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0021 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0025 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0027 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0002c0002 | 1/0 | 3198 | 41 | 28 | 2 | 0 | 5 | 5 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0002c0006 | 0/0 | 3198 | 4 | 4 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0002c0011 | 0/0 | 3198 | 2 | 0 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0003c0004 | 0/0 | 3198 | 8 | 6 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0004c0009 | 0/0 | 3198 | 3 | 0 | 2 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0004c0013 | 0/0 | 3198 | 2 | 0 | 0 | 0 | 0 | 2 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0005c0007 | 0/0 | 3198 | 3 | 3 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0006c0008 | 0/0 | 3198 | 3 | 2 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0007c0012 | 0/0 | 3198 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0008c0029 | 0/0 | 3198 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0009c0026 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0010c0022 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0011c0020 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0012c0017 | 0/0 | 3198 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0013c0016 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0014c0023 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0015c0024 | 0/0 | 3198 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0016c0015 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0017c0028 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4452 | 218 | 20 | 33 | 119 | 9 | 36 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0001t0002 | 0/0 | 4452 | 34 | 10 | 3 | 19 | 1 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0001t0003 | 0/0 | 4453 | 10 | 8 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0001t0004 | 0/0 | 4452 | 7 | 0 | 1 | 4 | 1 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0001t0006 | 0/0 | 4453 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0001t0008 | 0/0 | 4452 | 3 | 0 | 1 | 0 | 2 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0001t0010 | 0/0 | 4452 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0003t0001 | 0/0 | 4452 | 6 | 0 | 6 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0003t0007 | 0/0 | 4452 | 2 | 0 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0005t0001 | 0/0 | 4452 | 6 | 0 | 5 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0010t0001 | 0/0 | 4452 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0014t0001 | 0/0 | 4452 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0018t0001 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0019t0002 | 0/0 | 4452 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0021t0001 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0025t0001 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0001c0027t0001 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0002c0002t0001 | 1/0 | 4452 | 26 | 16 | 1 | 0 | 4 | 4 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0002c0002t0002 | 0/0 | 4452 | 6 | 6 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0002c0002t0003 | 0/0 | 4453 | 5 | 4 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0002c0002t0005 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0002c0002t0007 | 0/0 | 4452 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0002c0002t0009 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0002c0002t0011 | 0/0 | 4452 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0002c0006t0002 | 0/0 | 4452 | 4 | 4 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0002c0011t0002 | 0/0 | 4452 | 2 | 0 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0003c0004t0001 | 0/0 | 4452 | 5 | 3 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0003c0004t0002 | 0/0 | 4452 | 3 | 3 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0004c0009t0001 | 0/0 | 4452 | 3 | 0 | 2 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0004c0013t0002 | 0/0 | 4452 | 2 | 0 | 0 | 0 | 0 | 2 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0005c0007t0005 | 0/0 | 4453 | 3 | 3 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0006c0008t0001 | 0/0 | 4452 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0006c0008t0006 | 0/0 | 4453 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0007c0012t0001 | 0/0 | 4452 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0007c0012t0012 | 0/0 | 4452 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0008c0029t0001 | 0/0 | 4452 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0009c0026t0001 | 0/0 | 4452 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0010c0022t0001 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0011c0020t0002 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0012c0017t0007 | 0/0 | 4452 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0013c0016t0001 | 0/0 | 4452 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0014c0023t0001 | 0/0 | 4452 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0015c0024t0001 | 0/0 | 4452 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0016c0015t0009 | 0/0 | 4453 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
a0017c0028t0001 | 0/0 | 4452 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | copy fasta | chr3 | 149167497 | 149226829 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0024 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0006g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0008g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0008g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0010g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0001t0010g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0003t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0003t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0003t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0003t0007g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0005t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0005t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0005t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0005t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0005t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0005t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0010t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0010t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0014t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0018t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0019t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0021t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0025t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0001c0027t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0007g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0002t0011g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0006t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0006t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0006t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0006t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0002c0011t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0003c0004t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0004c0009t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0004c0009t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0004c0009t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0004c0013t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0005c0007t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0005c0007t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0005c0007t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0006c0008t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0006c0008t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0006c0008t0006g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0007c0012t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0007c0012t0012g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0008c0029t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0009c0026t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0010c0022t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0011c0020t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0012c0017t0007g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0013c0016t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0014c0023t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0015c0024t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0016c0015t0009g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
a0017c0028t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0317 | EUR | GBR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | FIN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | FIN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0263 | EUR | FIN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00408 | hp2 | a0001 | c0021 | t0001 | g0133 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | CHS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00733 | hp1 | a0001 | c0001 | t0008 | g0096 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00733 | hp2 | a0002 | c0011 | t0002 | g0014 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00735 | hp2 | a0002 | c0011 | t0002 | g0014 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0270 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00738 | hp2 | a0001 | c0005 | t0001 | g0043 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0089 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0326 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0327 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01081 | hp1 | a0015 | c0024 | t0001 | g0257 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0025 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01099 | hp2 | a0006 | c0008 | t0001 | g0166 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01106 | hp1 | a0001 | c0005 | t0001 | g0044 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01109 | hp1 | a0001 | c0005 | t0001 | g0032 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01109 | hp2 | a0008 | c0029 | t0001 | g0210 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0090 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01167 | hp2 | a0003 | c0004 | t0001 | g0309 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0091 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01169 | hp1 | a0003 | c0004 | t0001 | g0308 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0088 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01192 | hp1 | a0004 | c0009 | t0001 | g0260 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01243 | hp1 | a0002 | c0002 | t0003 | g0290 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0325 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01346 | hp2 | a0001 | c0003 | t0007 | g0092 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01358 | hp2 | a0001 | c0003 | t0007 | g0313 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0295 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0017 | EUR | IBS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01516 | hp1 | a0001 | c0001 | t0008 | g0010 | EUR | IBS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0320 | EUR | IBS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01517 | hp1 | a0001 | c0001 | t0008 | g0010 | EUR | IBS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0017 | EUR | IBS | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0336 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01952 | hp1 | a0001 | c0005 | t0001 | g0041 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG01993 | hp2 | a0001 | c0005 | t0001 | g0042 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02055 | hp2 | a0006 | c0008 | t0006 | g0220 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02074 | hp2 | a0001 | c0027 | t0001 | g0209 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0301 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0298 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02273 | hp2 | a0004 | c0009 | t0001 | g0078 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0294 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0296 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02572 | hp2 | a0007 | c0012 | t0012 | g0222 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0026 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02615 | hp1 | a0003 | c0004 | t0001 | g0311 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02615 | hp2 | a0006 | c0008 | t0006 | g0340 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02622 | hp1 | a0016 | c0015 | t0009 | g0314 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0300 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02630 | hp1 | a0003 | c0004 | t0002 | g0230 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0304 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02647 | hp2 | a0013 | c0016 | t0001 | g0100 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02683 | hp2 | a0002 | c0002 | t0007 | g0318 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02698 | hp2 | a0004 | c0013 | t0002 | g0012 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02717 | hp2 | a0017 | c0028 | t0001 | g0344 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02723 | hp1 | a0001 | c0010 | t0001 | g0226 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02735 | hp1 | a0004 | c0013 | t0002 | g0012 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0267 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0302 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0292 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02886 | hp2 | a0001 | c0010 | t0001 | g0225 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0338 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0272 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0224 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02922 | hp2 | a0003 | c0004 | t0002 | g0231 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02965 | hp1 | a0002 | c0002 | t0003 | g0286 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0297 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0341 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03098 | hp2 | a0002 | c0006 | t0002 | g0278 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03139 | hp1 | a0002 | c0006 | t0002 | g0277 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03195 | hp1 | a0003 | c0004 | t0002 | g0228 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03195 | hp2 | a0005 | c0007 | t0005 | g0315 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0305 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03225 | hp1 | a0002 | c0006 | t0002 | g0280 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0348 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03486 | hp1 | a0003 | c0004 | t0001 | g0310 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03486 | hp2 | a0001 | c0014 | t0001 | g0221 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03490 | hp1 | a0001 | c0019 | t0002 | g0183 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03516 | hp1 | a0007 | c0012 | t0001 | g0223 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03516 | hp2 | a0002 | c0006 | t0002 | g0279 | AFR | ESN | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03540 | hp2 | a0003 | c0004 | t0001 | g0229 | AFR | GWD | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0253 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0322 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03688 | hp1 | a0012 | c0017 | t0007 | g0306 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03710 | hp1 | a0004 | c0009 | t0001 | g0269 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0319 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0016 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | YRI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18522 | hp2 | a0005 | c0007 | t0005 | g0316 | AFR | YRI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18906 | hp1 | a0002 | c0002 | t0003 | g0288 | AFR | YRI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0299 | AFR | YRI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18945 | hp1 | a0001 | c0001 | t0010 | g0238 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18968 | hp2 | a0014 | c0023 | t0001 | g0156 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18972 | hp2 | a0010 | c0022 | t0001 | g0051 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18985 | hp1 | a0001 | c0005 | t0001 | g0040 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19012 | hp1 | a0001 | c0001 | t0010 | g0237 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19030 | hp1 | a0009 | c0026 | t0001 | g0162 | AFR | LWK | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0276 | AFR | LWK | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19043 | hp1 | a0002 | c0002 | t0005 | g0287 | AFR | LWK | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0284 | AFR | LWK | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19059 | hp2 | a0001 | c0025 | t0001 | g0066 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19064 | hp2 | a0001 | c0018 | t0001 | g0147 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19077 | hp1 | a0011 | c0020 | t0002 | g0164 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA19240 | hp2 | a0002 | c0002 | t0002 | g0282 | AFR | YRI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0275 | AFR | ASW | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0255 | EUR | TSI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | TSI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | TSI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20805 | hp2 | a0002 | c0002 | t0011 | g0321 | EUR | TSI | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | GIH | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | GIH | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02109 | hp1 | a0002 | c0002 | t0003 | g0291 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0342 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0293 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | ACB | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0303 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG03471 | hp2 | a0002 | c0002 | t0003 | g0289 | AFR | MSL | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG06807 | hp1 | a0005 | c0007 | t0005 | g0307 | AFR | USA | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | USA | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0334 | AFR | USA | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | USA | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA21309 | hp1 | a0002 | c0002 | t0009 | g0093 | AFR | LWK | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0281 | AFR | LWK | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0024 | REF | REF | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0227 | REF | REF | CP_chr3_149167497_149226829 | CP | chr3 | 149167497 | 149226829 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149177860
|
C | T | 1 | a0011 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.2998G>A | p.Gly1000Ser | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/19 | 3035/4452 | 2998/3198 | 1000/1065 | chr3 | 149177860 | ||
chr3:149179596
|
C | T | 1 | a0012 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.2621G>A | p.Cys874Tyr | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/19 | 2658/4452 | 2621/3198 | 874/1065 | chr3 | 149179596 | ||
chr3:149182034
|
T | C | 1 | a0007 | 2 | HG02572.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.2525A>G | p.Glu842Gly | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/19 | 2562/4452 | 2525/3198 | 842/1065 | chr3 | 149182034 | ||
chr3:149183513
|
C | T | 1 | a0006 | 3 | HG01099.hp2 HG02055.hp2 HG02615.hp2 |
missense_variant | MODERATE | c.2378G>A | p.Arg793His | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/19 | 2415/4452 | 2378/3198 | 793/1065 | chr3 | 149183513 | ||
chr3:149186652
|
C | T | 1 | a0013 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1945G>A | p.Ala649Thr | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/19 | 1982/4452 | 1945/3198 | 649/1065 | chr3 | 149186652 | ||
chr3:149188142
|
G | A | 1 | a0010 | 1 | NA18972.hp2 | missense_variant | MODERATE | c.1774C>T | p.Leu592Phe | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 10/19 | 1811/4452 | 1774/3198 | 592/1065 | chr3 | 149188142 | ||
chr3:149198428
|
G | A | 1 | a0004 | 5 | HG01192.hp1 HG02273.hp2 HG02698.hp2 others(2): Show |
missense_variant | MODERATE | c.1652C>T | p.Thr551Ile | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/19 | 1689/4452 | 1652/3198 | 551/1065 | chr3 | 149198428 | ||
chr3:149198448
|
T | A | 15 | a0001a0003a0004others(12): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(325): Show |
missense_variant | MODERATE | c.1632A>T | p.Glu544Asp | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/19 | 1669/4452 | 1632/3198 | 544/1065 | chr3 | 149198448 | ||
chr3:149199720
|
T | C | 1 | a0014 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.1493A>G | p.Gln498Arg | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 8/19 | 1530/4452 | 1493/3198 | 498/1065 | chr3 | 149199720 | ||
chr3:149202185
|
T | C | 1 | a0015 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1265A>G | p.Lys422Arg | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/19 | 1302/4452 | 1265/3198 | 422/1065 | chr3 | 149202185 | ||
chr3:149206277
|
G | A | 1 | a0003 | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
missense_variant | MODERATE | c.1099C>T | p.Arg367Cys | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/19 | 1136/4452 | 1099/3198 | 367/1065 | chr3 | 149206277 | ||
chr3:149209276
|
T | A | 1 | a0009 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.716A>T | p.Tyr239Phe | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/19 | 753/4452 | 716/3198 | 239/1065 | chr3 | 149209276 | ||
chr3:149210317
|
C | T | 1 | a0016 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.457G>A | p.Glu153Lys | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/19 | 494/4452 | 457/3198 | 153/1065 | chr3 | 149210317 | ||
chr3:149212498
|
G | T | 1 | a0005 | 3 | HG03195.hp2 HG06807.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.347C>A | p.Pro116His | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/19 | 384/4452 | 347/3198 | 116/1065 | chr3 | 149212498 | ||
chr3:149212523
|
G | A | 1 | a0017 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.322C>T | p.His108Tyr | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/19 | 359/4452 | 322/3198 | 108/1065 | chr3 | 149212523 | ||
chr3:149212609
|
G | A | 1 | a0008 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.236C>T | p.Thr79Ile | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/19 | 273/4452 | 236/3198 | 79/1065 | chr3 | 149212609 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149177861
|
G | A | 1 | a0001c0021 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.2997C>T | p.His999His | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/19 | 3034/4452 | 2997/3198 | 999/1065 | chr3 | 149177861 | ||
chr3:149177867
|
A | G | 3 | a0001c0019a0002c0011a0004c0013 | 5 | HG00733.hp2 HG00735.hp2 HG02698.hp2 others(2): Show |
synonymous_variant | LOW | c.2991T>C | p.His997His | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/19 | 3028/4452 | 2991/3198 | 997/1065 | chr3 | 149177867 | ||
chr3:149178596
|
A | G | 1 | a0001c0018 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.2697T>C | p.Val899Val | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 16/19 | 2734/4452 | 2697/3198 | 899/1065 | chr3 | 149178596 | ||
chr3:149186647
|
T | G | 1 | a0001c0003 | 8 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
synonymous_variant | LOW | c.1950A>C | p.Gly650Gly | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/19 | 1987/4452 | 1950/3198 | 650/1065 | chr3 | 149186647 | ||
chr3:149202175
|
A | G | 1 | a0001c0010 | 2 | HG02723.hp1 HG02886.hp2 |
synonymous_variant | LOW | c.1275T>C | p.Tyr425Tyr | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/19 | 1312/4452 | 1275/3198 | 425/1065 | chr3 | 149202175 | ||
chr3:149206338
|
G | A | 1 | a0001c0025 | 1 | NA19059.hp2 | splice_region_variant&synonymous_variant | LOW | c.1038C>T | p.Ala346Ala | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/19 | 1075/4452 | 1038/3198 | 346/1065 | chr3 | 149206338 | ||
chr3:149207406
|
A | G | 1 | a0001c0005 | 6 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(3): Show |
synonymous_variant | LOW | c.993T>C | p.Pro331Pro | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/19 | 1030/4452 | 993/3198 | 331/1065 | chr3 | 149207406 | ||
chr3:149209323
|
C | G | 1 | a0002c0006 | 4 | HG03098.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.669G>C | p.Val223Val | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/19 | 706/4452 | 669/3198 | 223/1065 | chr3 | 149209323 | ||
chr3:149210306
|
T | G | 1 | a0001c0027 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.468A>C | p.Thr156Thr | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/19 | 505/4452 | 468/3198 | 156/1065 | chr3 | 149210306 | ||
chr3:149212584
|
C | T | 1 | a0001c0014 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.261G>A | p.Pro87Pro | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/19 | 298/4452 | 261/3198 | 87/1065 | chr3 | 149212584 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149172557
|
G | A | 1 | a0001c0001t0004 | 7 | HG00323.hp1 HG00597.hp1 HG01081.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1157C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 1157 | chr3 | 149172557 | |||||
chr3:149172802
|
G | C | 1 | a0001c0001t0010 | 2 | NA18945.hp1 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*912C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 912 | chr3 | 149172802 | |||||
chr3:149172835
|
T | G | 2 | a0001c0001t0006a0006c0008t0006 | 4 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*879A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 879 | chr3 | 149172835 | |||||
chr3:149172885
|
A | AT | 8 | a0001c0001t0003a0001c0001t0006a0002c0002t0003others(5): Show | 25 | HG00738.hp1 HG01243.hp1 HG01255.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*828dupA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 828 | chr3 | 149172885 | |||||
chr3:149172945
|
C | T | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(13): Show | 78 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*769G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 769 | chr3 | 149172945 | |||||
chr3:149172946
|
A | G | 4 | a0002c0002t0005a0002c0002t0009a0005c0007t0005others(1): Show | 6 | HG02622.hp1 HG03195.hp2 HG06807.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*768T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 768 | chr3 | 149172946 | |||||
chr3:149173205
|
T | G | 1 | a0001c0001t0008 | 3 | HG00733.hp1 HG01516.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*509A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 509 | chr3 | 149173205 | |||||
chr3:149173240
|
A | G | 2 | a0002c0002t0005a0005c0007t0005 | 4 | HG03195.hp2 HG06807.hp1 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*474T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 474 | chr3 | 149173240 | |||||
chr3:149173341
|
G | C | 1 | a0002c0002t0011 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 373 | chr3 | 149173341 | |||||
chr3:149173455
|
G | A | 1 | a0007c0012t0012 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*259C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 259 | chr3 | 149173455 | |||||
chr3:149173577
|
G | A | 3 | a0001c0003t0007a0002c0002t0007a0012c0017t0007 | 4 | HG01346.hp2 HG01358.hp2 HG02683.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*137C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 19/19 | 137 | chr3 | 149173577 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:149173734
|
T | C | 4 | a0001c0001t0006g0267a0001c0001t0006g0284a0006c0008t0006g0220others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.3182-4A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149173734 | ||||||
chr3:149173862
|
A | G | 11 | a0001c0001t0001g0018a0001c0001t0001g0122a0001c0001t0001g0131others(8): Show | 12 | HG01109.hp1 HG01192.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.3182-132T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149173862 | ||||||
chr3:149174041
|
T | C | 4 | a0001c0003t0007g0092a0001c0003t0007g0313a0002c0002t0007g0318others(1): Show | 4 | HG01346.hp2 HG01358.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.3182-311A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149174041 | ||||||
chr3:149174094
|
A | G | 5 | a0001c0001t0001g0274a0002c0002t0001g0015a0002c0002t0001g0292others(2): Show | 6 | HG02258.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3182-364T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149174094 | ||||||
chr3:149174125
|
A | T | 1 | a0001c0001t0001g0145 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3182-395T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149174125 | ||||||
chr3:149174180
|
T | G | 349 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(346): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.3182-450A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149174180 | ||||||
chr3:149174387
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3182-657A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149174387 | ||||||
chr3:149174703
|
A | C | 1 | a0001c0001t0001g0049 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.3182-973T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149174703 | ||||||
chr3:149175148
|
T | A | 1 | a0002c0002t0009g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3181+1102A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175148 | ||||||
chr3:149175149
|
T | A | 1 | a0002c0002t0009g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3181+1101A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175149 | ||||||
chr3:149175150
|
T | G | 1 | a0002c0002t0009g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3181+1100A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175150 | ||||||
chr3:149175296
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3181+954A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175296 | ||||||
chr3:149175339
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0109 | 3 | NA18965.hp1 NA18981.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.3181+911C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175339 | ||||||
chr3:149175449
|
A | G | 1 | a0002c0002t0001g0304 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3181+801T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175449 | ||||||
chr3:149175664
|
A | AGT | 15 | a0001c0001t0001g0062a0001c0001t0001g0120a0001c0001t0001g0152others(12): Show | 16 | HG00408.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.3181+584_3181+585d others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | ||||||
chr3:149175664
|
A | AGTGTGTG others(3): Show |
15 | a0001c0001t0003g0178a0001c0001t0003g0271a0001c0001t0003g0272others(12): Show | 15 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.3181+576_3181+585d others(12): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | ||||||
chr3:149175664
|
A | AGTGTGTG others(5): Show |
45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(42): Show | 47 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.3181+574_3181+585d others(14): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | ||||||
chr3:149175664
|
A | AGTGTGTG others(7): Show |
42 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0049others(39): Show | 45 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.3181+572_3181+585d others(16): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | ||||||
chr3:149175664
|
A | AGTGTGTG others(9): Show |
7 | a0001c0001t0002g0157a0001c0001t0002g0163a0001c0001t0002g0256others(4): Show | 7 | HG01346.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3181+570_3181+585d others(18): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | ||||||
chr3:149175664
|
A | AGTGTGTG others(11): Show |
11 | a0001c0001t0002g0001a0001c0001t0002g0250a0001c0001t0002g0251others(8): Show | 14 | HG01070.hp2 HG01071.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.3181+568_3181+585d others(20): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | ||||||
chr3:149175664
|
A | AGTGTGTG others(13): Show |
2 | a0001c0001t0003g0253a0004c0013t0002g0012 | 3 | HG02698.hp2 HG02735.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3181+566_3181+585d others(22): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | ||||||
chr3:149175664
|
A | AGTGTGTG others(15): Show |
3 | a0001c0001t0003g0254a0001c0001t0006g0284a0006c0008t0006g0340 | 3 | HG02615.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3181+564_3181+585d others(24): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | ||||||
chr3:149175664
|
A | AGTGTGTG others(17): Show |
4 | a0001c0001t0003g0233a0001c0001t0003g0234a0001c0001t0003g0270others(1): Show | 5 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.3181+562_3181+585d others(26): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175664 | ||||||
chr3:149175667
|
G | GTGTGTGT others(7): Show |
1 | a0016c0015t0009g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3181+582_3181+583i others(16): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175667 | ||||||
chr3:149175783
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3181+467T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175783 | ||||||
chr3:149175877
|
C | T | 5 | a0001c0001t0003g0233a0001c0001t0003g0234a0001c0001t0003g0270others(2): Show | 5 | HG00738.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.3181+373G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149175877 | ||||||
chr3:149176003
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0145 | 2 | NA18949.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.3181+247T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149176003 | ||||||
chr3:149176004
|
C | T | 1 | a0015c0024t0001g0257 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3181+246G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 18/18 | chr3 | 149176004 | ||||||
chr3:149176570
|
T | G | 3 | a0001c0019t0002g0183a0002c0011t0002g0014a0004c0013t0002g0012 | 5 | HG00733.hp2 HG00735.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.3019-158A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149176570 | ||||||
chr3:149176577
|
A | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0261a0001c0001t0001g0262 | 3 | HG00323.hp2 HG01255.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3019-165T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149176577 | ||||||
chr3:149176878
|
C | T | 1 | a0001c0005t0001g0042 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3019-466G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149176878 | ||||||
chr3:149176898
|
A | T | 1 | a0001c0001t0001g0239 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3019-486T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149176898 | ||||||
chr3:149176901
|
A | G | 5 | a0001c0001t0002g0001a0001c0001t0002g0250a0001c0001t0002g0251others(2): Show | 8 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3019-489T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149176901 | ||||||
chr3:149177243
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3018+597T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149177243 | ||||||
chr3:149177264
|
C | T | 6 | a0002c0002t0005g0287a0002c0002t0009g0093a0005c0007t0005g0307others(3): Show | 6 | HG02622.hp1 HG03195.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.3018+576G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149177264 | ||||||
chr3:149177339
|
A | G | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(54): Show | 59 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.3018+501T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149177339 | ||||||
chr3:149177744
|
G | C | 20 | a0001c0001t0001g0022a0001c0001t0001g0046a0001c0001t0001g0067others(17): Show | 21 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.3018+96C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 17/18 | chr3 | 149177744 | ||||||
chr3:149178044
|
A | C | 5 | a0001c0001t0002g0003a0001c0001t0002g0063a0001c0001t0002g0285others(2): Show | 7 | HG00408.hp1 HG00673.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.2879-65T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 16/18 | chr3 | 149178044 | ||||||
chr3:149178218
|
G | A | 7 | a0001c0001t0003g0233a0001c0001t0003g0234a0001c0001t0003g0253others(4): Show | 7 | HG00738.hp1 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2878+197C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 16/18 | chr3 | 149178218 | ||||||
chr3:149178318
|
T | C | 11 | a0001c0001t0003g0233a0001c0001t0003g0234a0001c0001t0003g0253others(8): Show | 11 | HG00738.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2878+97A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 16/18 | chr3 | 149178318 | ||||||
chr3:149178359
|
T | G | 1 | a0001c0001t0001g0186 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2878+56A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 16/18 | chr3 | 149178359 | ||||||
chr3:149178403
|
A | C | 5 | a0001c0001t0001g0274a0002c0002t0001g0015a0002c0002t0001g0292others(2): Show | 6 | HG02258.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2878+12T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 16/18 | chr3 | 149178403 | ||||||
chr3:149178643
|
A | G | 124 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(121): Show | 134 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.2662-12T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149178643 | ||||||
chr3:149178754
|
A | G | 6 | a0002c0002t0005g0287a0002c0002t0009g0093a0005c0007t0005g0307others(3): Show | 6 | HG02622.hp1 HG03195.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.2662-123T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149178754 | ||||||
chr3:149178764
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2662-133A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149178764 | ||||||
chr3:149178947
|
A | G | 7 | a0001c0001t0003g0233a0001c0001t0003g0234a0001c0001t0003g0253others(4): Show | 7 | HG00738.hp1 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2662-316T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149178947 | ||||||
chr3:149179033
|
A | G | 57 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(54): Show | 59 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.2662-402T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149179033 | ||||||
chr3:149179047
|
T | C | 14 | a0001c0001t0001g0274a0001c0001t0003g0178a0001c0001t0003g0334others(11): Show | 15 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.2662-416A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149179047 | ||||||
chr3:149179242
|
C | T | 1 | a0001c0001t0002g0248 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2661+314G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149179242 | ||||||
chr3:149179423
|
A | C | 6 | a0001c0001t0001g0274a0002c0002t0001g0015a0002c0002t0001g0292others(3): Show | 7 | HG02258.hp1 HG02486.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2661+133T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 15/18 | chr3 | 149179423 | ||||||
chr3:149179711
|
T | TAC | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(91): Show | 99 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.2555-51_2555-50dup others(2): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | ||||||
chr3:149179711
|
T | TACAC | 46 | a0001c0001t0001g0018a0001c0001t0001g0033a0001c0001t0001g0035others(43): Show | 47 | HG00280.hp2 HG00544.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.2555-53_2555-50dup others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | ||||||
chr3:149179711
|
T | TACACAC | 36 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0077others(33): Show | 36 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.2555-55_2555-50dup others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | ||||||
chr3:149179711
|
T | TACACACA others(1): Show |
12 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0039others(9): Show | 14 | HG00597.hp2 HG02071.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.2555-57_2555-50dup others(8): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | ||||||
chr3:149179711
|
TAC | T | 26 | a0001c0001t0001g0056a0001c0001t0001g0159a0001c0001t0001g0214others(23): Show | 29 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.2555-51_2555-50del others(2): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | ||||||
chr3:149179711
|
TACAC | T | 21 | a0001c0001t0001g0050a0001c0001t0001g0082a0001c0001t0001g0104others(18): Show | 23 | HG00280.hp1 HG01070.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.2555-53_2555-50del others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | ||||||
chr3:149179711
|
TACACAC | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0120others(3): Show | 8 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2555-55_2555-50del others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | ||||||
chr3:149179711
|
TACACACA others(1): Show |
T | 3 | a0001c0001t0001g0054a0001c0001t0001g0241a0007c0012t0012g0222 | 3 | HG02572.hp2 NA19063.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2555-57_2555-50del others(8): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179711 | ||||||
chr3:149179830
|
AGGAATTT others(16): Show |
A | 5 | a0001c0001t0001g0274a0002c0002t0001g0015a0002c0002t0001g0292others(2): Show | 6 | HG02258.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2555-191_2555-169d others(25): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179830 | ||||||
chr3:149179941
|
C | A | 1 | a0002c0002t0002g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2555-279G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149179941 | ||||||
chr3:149180022
|
A | G | 5 | a0001c0001t0001g0274a0002c0002t0001g0015a0002c0002t0001g0292others(2): Show | 6 | HG02258.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2555-360T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180022 | ||||||
chr3:149180177
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2555-515G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180177 | ||||||
chr3:149180214
|
G | A | 13 | a0001c0001t0001g0013a0001c0001t0001g0081a0001c0001t0001g0103others(10): Show | 14 | HG00609.hp1 HG01258.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.2555-552C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180214 | ||||||
chr3:149180299
|
A | G | 7 | a0002c0002t0002g0301a0002c0002t0005g0287a0002c0002t0009g0093others(4): Show | 7 | HG02257.hp1 HG02622.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2555-637T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180299 | ||||||
chr3:149180306
|
A | G | 4 | a0001c0001t0001g0110a0001c0001t0001g0155a0001c0001t0001g0158others(1): Show | 4 | HG02040.hp2 NA18966.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.2555-644T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180306 | ||||||
chr3:149180315
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2555-653G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180315 | ||||||
chr3:149180318
|
G | A | 1 | a0002c0002t0002g0282 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2555-656C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180318 | ||||||
chr3:149180388
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0247a0001c0001t0001g0249 | 3 | NA18963.hp1 NA18980.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.2555-726A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180388 | ||||||
chr3:149180416
|
C | A | 3 | a0001c0003t0007g0092a0001c0003t0007g0313a0002c0002t0007g0318 | 3 | HG01346.hp2 HG01358.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.2555-754G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180416 | ||||||
chr3:149180722
|
G | T | 1 | a0002c0002t0001g0299 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2555-1060C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180722 | ||||||
chr3:149180751
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2555-1089C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180751 | ||||||
chr3:149180867
|
G | T | 6 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0339others(3): Show | 6 | HG02647.hp1 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2554+1138C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180867 | ||||||
chr3:149180872
|
T | A | 5 | a0001c0001t0001g0274a0002c0002t0001g0015a0002c0002t0001g0292others(2): Show | 6 | HG02258.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2554+1133A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149180872 | ||||||
chr3:149181005
|
C | CGAT | 79 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(76): Show | 81 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.2554+997_2554+999d others(5): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181005 | ||||||
chr3:149181158
|
G | A | 1 | a0001c0001t0006g0284 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2554+847C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181158 | ||||||
chr3:149181388
|
C | T | 4 | a0001c0003t0007g0092a0001c0003t0007g0313a0002c0002t0007g0318others(1): Show | 4 | HG01346.hp2 HG01358.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.2554+617G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181388 | ||||||
chr3:149181452
|
A | C | 85 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(82): Show | 88 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.2554+553T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181452 | ||||||
chr3:149181487
|
A | T | 1 | a0002c0002t0001g0299 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2554+518T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181487 | ||||||
chr3:149181602
|
T | G | 90 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(87): Show | 95 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.2554+403A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181602 | ||||||
chr3:149181647
|
C | G | 2 | a0002c0002t0001g0299a0002c0002t0002g0338 | 2 | HG02895.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2554+358G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181647 | ||||||
chr3:149181675
|
A | G | 86 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0020others(83): Show | 90 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.2554+330T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181675 | ||||||
chr3:149181675
|
A | T | 18 | a0001c0001t0001g0022a0001c0001t0001g0104a0001c0001t0001g0142others(15): Show | 19 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.2554+330T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181675 | ||||||
chr3:149181721
|
G | A | 2 | a0007c0012t0001g0223a0007c0012t0012g0222 | 2 | HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2554+284C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181721 | ||||||
chr3:149181761
|
C | T | 1 | a0001c0018t0001g0147 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2554+244G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181761 | ||||||
chr3:149181783
|
T | C | 21 | a0001c0001t0001g0020a0001c0001t0001g0274a0001c0001t0001g0339others(18): Show | 23 | HG01243.hp1 HG01243.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.2554+222A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181783 | ||||||
chr3:149181848
|
T | G | 1 | a0001c0001t0001g0347 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2554+157A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181848 | ||||||
chr3:149181909
|
C | T | 10 | a0001c0001t0001g0020a0001c0001t0001g0339a0001c0001t0001g0346others(7): Show | 11 | HG01243.hp2 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.2554+96G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181909 | ||||||
chr3:149181988
|
C | T | 6 | a0001c0001t0001g0214a0001c0003t0001g0008a0001c0003t0001g0088others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.2554+17G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 14/18 | chr3 | 149181988 | ||||||
chr3:149182185
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2426-52A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182185 | ||||||
chr3:149182259
|
C | T | 44 | a0001c0001t0001g0020a0001c0001t0001g0274a0001c0001t0001g0343others(41): Show | 47 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.2426-126G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182259 | ||||||
chr3:149182371
|
G | A | 1 | a0007c0012t0012g0222 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2426-238C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182371 | ||||||
chr3:149182381
|
T | C | 8 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(5): Show | 9 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2426-248A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182381 | ||||||
chr3:149182382
|
G | A | 1 | a0001c0001t0004g0101 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2426-249C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182382 | ||||||
chr3:149182422
|
T | C | 50 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0274others(47): Show | 54 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.2426-289A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182422 | ||||||
chr3:149182489
|
A | G | 5 | a0001c0003t0001g0008a0001c0003t0001g0088a0001c0003t0001g0091others(2): Show | 6 | HG01069.hp2 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.2426-356T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182489 | ||||||
chr3:149182610
|
T | C | 1 | a0002c0002t0009g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2426-477A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182610 | ||||||
chr3:149182687
|
G | A | 21 | a0001c0001t0001g0274a0001c0014t0001g0221a0002c0002t0001g0015others(18): Show | 22 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.2426-554C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182687 | ||||||
chr3:149182812
|
G | A | 42 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0333others(39): Show | 46 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.2425+654C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182812 | ||||||
chr3:149182923
|
G | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0346a0001c0001t0001g0347others(1): Show | 5 | HG01243.hp2 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2425+543C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182923 | ||||||
chr3:149182925
|
C | T | 20 | a0001c0014t0001g0221a0002c0002t0001g0015a0002c0002t0001g0292others(17): Show | 21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.2425+541G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149182925 | ||||||
chr3:149183074
|
A | C | 55 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0333others(52): Show | 60 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.2425+392T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183074 | ||||||
chr3:149183116
|
A | G | 41 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(38): Show | 45 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2425+350T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183116 | ||||||
chr3:149183129
|
C | T | 35 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(32): Show | 38 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2425+337G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183129 | ||||||
chr3:149183130
|
G | A | 2 | a0001c0001t0002g0150a0001c0001t0002g0171 | 2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2425+336C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183130 | ||||||
chr3:149183207
|
C | A | 41 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(38): Show | 45 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2425+259G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183207 | ||||||
chr3:149183242
|
C | T | 2 | a0001c0005t0001g0040a0001c0025t0001g0066 | 2 | NA18985.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.2425+224G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183242 | ||||||
chr3:149183243
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(2): Show | 6 | HG01884.hp1 HG02257.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2425+223C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183243 | ||||||
chr3:149183257
|
T | C | 2 | a0007c0012t0001g0223a0007c0012t0012g0222 | 2 | HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2425+209A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183257 | ||||||
chr3:149183291
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2425+175T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183291 | ||||||
chr3:149183403
|
C | T | 1 | a0002c0002t0005g0287 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2425+63G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183403 | ||||||
chr3:149183404
|
G | A | 1 | a0002c0002t0009g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2425+62C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 13/18 | chr3 | 149183404 | ||||||
chr3:149183617
|
A | C | 5 | a0002c0002t0001g0302a0002c0002t0001g0304a0002c0002t0001g0305others(2): Show | 5 | HG02630.hp2 HG02809.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2286-12T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149183617 | ||||||
chr3:149183619
|
AC | A | 69 | a0001c0001t0001g0019a0001c0001t0001g0172a0001c0001t0001g0181others(66): Show | 73 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.2286-15delG | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149183619 | ||||||
chr3:149183620
|
C | A | 2 | a0001c0001t0003g0334a0001c0001t0003g0336 | 2 | HG01884.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2286-15G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149183620 | ||||||
chr3:149183753
|
C | A | 41 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(38): Show | 45 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2286-148G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149183753 | ||||||
chr3:149183899
|
C | A | 1 | a0002c0002t0009g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2286-294G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149183899 | ||||||
chr3:149184023
|
TA | T | 26 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0188others(23): Show | 26 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.2286-419delT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184023 | ||||||
chr3:149184026
|
TTC | T | 22 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0217others(19): Show | 22 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.2286-423_2286-422d others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184026 | ||||||
chr3:149184027
|
TC | T | 4 | a0001c0001t0001g0188a0001c0001t0001g0194a0001c0001t0001g0245others(1): Show | 4 | HG01175.hp1 HG01175.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2286-423delG | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184027 | ||||||
chr3:149184028
|
C | CT | 67 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(64): Show | 71 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.2286-424dupA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | ||||||
chr3:149184028
|
C | CTT | 95 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0020others(92): Show | 100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.2286-425_2286-424d others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | ||||||
chr3:149184028
|
C | CTTT | 35 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0097others(32): Show | 35 | HG00558.hp2 HG00642.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.2286-426_2286-424d others(5): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | ||||||
chr3:149184028
|
C | CTTTT | 15 | a0001c0001t0001g0013a0001c0001t0001g0103a0001c0001t0001g0109others(12): Show | 16 | HG00609.hp1 HG01258.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2286-427_2286-424d others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | ||||||
chr3:149184028
|
C | CTTTTT | 6 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0003t0001g0008others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.2286-428_2286-424d others(7): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | ||||||
chr3:149184028
|
CT | C | 7 | a0001c0001t0001g0241a0001c0001t0002g0312a0001c0001t0002g0327others(4): Show | 7 | HG01071.hp2 HG02895.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2286-424delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | ||||||
chr3:149184028
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0064 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2286-437_2286-424d others(16): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | ||||||
chr3:149184028
|
CTTTTTTT others(8): Show |
C | 1 | a0002c0002t0011g0321 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2286-438_2286-424d others(17): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184028 | ||||||
chr3:149184118
|
C | T | 41 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(38): Show | 45 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.2286-513G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184118 | ||||||
chr3:149184196
|
A | G | 35 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(32): Show | 38 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2286-591T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184196 | ||||||
chr3:149184270
|
C | T | 35 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(32): Show | 38 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2286-665G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184270 | ||||||
chr3:149184279
|
C | G | 6 | a0001c0003t0001g0008a0001c0003t0001g0088a0001c0003t0001g0090others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.2286-674G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184279 | ||||||
chr3:149184314
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2286-709G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184314 | ||||||
chr3:149184325
|
G | A | 34 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(31): Show | 37 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.2286-720C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184325 | ||||||
chr3:149184334
|
C | G | 1 | a0002c0002t0003g0289 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2286-729G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184334 | ||||||
chr3:149184513
|
C | T | 19 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(16): Show | 22 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.2285+726G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184513 | ||||||
chr3:149184536
|
A | G | 20 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(17): Show | 23 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.2285+703T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184536 | ||||||
chr3:149184546
|
C | T | 21 | a0001c0014t0001g0221a0002c0002t0001g0015a0002c0002t0001g0292others(18): Show | 22 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.2285+693G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184546 | ||||||
chr3:149184568
|
G | A | 13 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(10): Show | 15 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.2285+671C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184568 | ||||||
chr3:149184636
|
A | G | 1 | a0002c0002t0009g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2285+603T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184636 | ||||||
chr3:149184654
|
C | CTAA | 20 | a0001c0014t0001g0221a0002c0002t0001g0015a0002c0002t0001g0292others(17): Show | 21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.2285+582_2285+584d others(5): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184654 | ||||||
chr3:149184809
|
G | T | 2 | a0001c0010t0001g0225a0001c0010t0001g0226 | 2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2285+430C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184809 | ||||||
chr3:149184895
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2285+344C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184895 | ||||||
chr3:149184927
|
T | C | 30 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0188others(27): Show | 30 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.2285+312A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149184927 | ||||||
chr3:149185029
|
G | T | 1 | a0001c0001t0001g0168 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2285+210C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149185029 | ||||||
chr3:149185068
|
G | A | 20 | a0001c0014t0001g0221a0002c0002t0001g0015a0002c0002t0001g0292others(17): Show | 21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.2285+171C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149185068 | ||||||
chr3:149185097
|
G | A | 4 | a0001c0003t0001g0008a0001c0003t0001g0088a0001c0003t0001g0090others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.2285+142C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149185097 | ||||||
chr3:149185101
|
TTTG | T | 40 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(37): Show | 44 | HG00733.hp2 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.2285+135_2285+137d others(5): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149185101 | ||||||
chr3:149185142
|
CT | C | 21 | a0001c0001t0001g0235a0001c0014t0001g0221a0002c0002t0001g0015others(18): Show | 22 | HG01243.hp1 HG01261.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2285+96delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149185142 | ||||||
chr3:149185163
|
T | C | 6 | a0001c0003t0001g0008a0001c0003t0001g0088a0001c0003t0001g0090others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.2285+76A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 12/18 | chr3 | 149185163 | ||||||
chr3:149185579
|
C | T | 2 | a0007c0012t0001g0223a0007c0012t0012g0222 | 2 | HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2078-133G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185579 | ||||||
chr3:149185590
|
A | ACATAG | 17 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(14): Show | 19 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.2078-145_2078-144i others(7): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185590 | ||||||
chr3:149185591
|
T | G | 17 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(14): Show | 19 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.2078-145A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185591 | ||||||
chr3:149185593
|
C | G | 17 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(14): Show | 19 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.2078-147G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185593 | ||||||
chr3:149185618
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0218 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2078-172T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185618 | ||||||
chr3:149185638
|
A | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(14): Show | 19 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.2078-192T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185638 | ||||||
chr3:149185644
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | NA19086.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2078-198G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185644 | ||||||
chr3:149185646
|
C | T | 17 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(14): Show | 19 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.2078-200G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185646 | ||||||
chr3:149185709
|
G | A | 37 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(34): Show | 40 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.2078-263C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185709 | ||||||
chr3:149185757
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2078-311G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185757 | ||||||
chr3:149185840
|
G | A | 26 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0150others(23): Show | 32 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.2078-394C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185840 | ||||||
chr3:149185864
|
T | A | 1 | a0001c0001t0001g0167 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2078-418A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185864 | ||||||
chr3:149185927
|
G | A | 19 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(16): Show | 21 | HG00733.hp2 HG00735.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.2078-481C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185927 | ||||||
chr3:149185934
|
G | A | 1 | a0002c0002t0005g0287 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2078-488C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149185934 | ||||||
chr3:149186049
|
T | C | 20 | a0001c0014t0001g0221a0002c0002t0001g0015a0002c0002t0001g0292others(17): Show | 21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.2077+471A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149186049 | ||||||
chr3:149186128
|
A | G | 6 | a0002c0002t0001g0298a0002c0002t0001g0299a0002c0002t0002g0301others(3): Show | 6 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2077+392T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149186128 | ||||||
chr3:149186136
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(138): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.2077+384C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149186136 | ||||||
chr3:149186371
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2077+149A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 11/18 | chr3 | 149186371 | ||||||
chr3:149187220
|
T | A | 256 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(253): Show | 274 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.1865-488A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 10/18 | chr3 | 149187220 | ||||||
chr3:149187496
|
C | T | 22 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0250others(19): Show | 28 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1864+556G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 10/18 | chr3 | 149187496 | ||||||
chr3:149187533
|
C | G | 1 | a0017c0028t0001g0344 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1864+519G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 10/18 | chr3 | 149187533 | ||||||
chr3:149187723
|
G | A | 9 | a0001c0001t0001g0235a0001c0001t0001g0242a0001c0001t0001g0243others(6): Show | 9 | HG00738.hp1 HG01099.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1864+329C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 10/18 | chr3 | 149187723 | ||||||
chr3:149187939
|
G | A | 7 | a0001c0003t0001g0008a0001c0003t0001g0088a0001c0003t0001g0089others(4): Show | 8 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1864+113C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 10/18 | chr3 | 149187939 | ||||||
chr3:149187990
|
A | G | 17 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(14): Show | 19 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.1864+62T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 10/18 | chr3 | 149187990 | ||||||
chr3:149188226
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1714-24A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188226 | ||||||
chr3:149188240
|
A | G | 38 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(35): Show | 41 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.1714-38T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188240 | ||||||
chr3:149188379
|
G | C | 1 | a0001c0001t0001g0243 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1714-177C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188379 | ||||||
chr3:149188490
|
C | CA | 136 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0013others(133): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1714-289dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | ||||||
chr3:149188490
|
C | CAA | 47 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0021others(44): Show | 54 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1714-290_1714-289d others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | ||||||
chr3:149188490
|
C | CAAA | 17 | a0001c0001t0001g0022a0001c0001t0001g0160a0001c0001t0001g0206others(14): Show | 18 | HG00609.hp1 HG00741.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1714-291_1714-289d others(5): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | ||||||
chr3:149188490
|
C | CAAAA | 13 | a0001c0001t0001g0121a0001c0001t0001g0181a0001c0001t0001g0188others(10): Show | 13 | HG00738.hp1 HG01261.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.1714-292_1714-289d others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | ||||||
chr3:149188490
|
C | CAAAAA | 13 | a0001c0001t0001g0172a0001c0001t0001g0194a0001c0001t0001g0217others(10): Show | 13 | HG01069.hp1 HG01081.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1714-293_1714-289d others(7): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | ||||||
chr3:149188490
|
CA | C | 8 | a0001c0001t0001g0029a0001c0001t0001g0075a0001c0001t0001g0106others(5): Show | 9 | HG00099.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1714-289delT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | ||||||
chr3:149188490
|
CAAAAAA | C | 19 | a0001c0014t0001g0221a0002c0002t0001g0015a0002c0002t0001g0292others(16): Show | 20 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1714-294_1714-289d others(8): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | ||||||
chr3:149188490
|
CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0001g0204a0001c0003t0001g0008a0001c0003t0001g0088others(4): Show | 8 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714-296_1714-289d others(10): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | ||||||
chr3:149188490
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0203 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1714-298_1714-289d others(12): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | ||||||
chr3:149188490
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0010t0001g0225a0001c0010t0001g0226 | 2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1714-301_1714-289d others(15): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | ||||||
chr3:149188490
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0004 | 2 | NA18975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1714-302_1714-289d others(16): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188490 | ||||||
chr3:149188491
|
A | C | 2 | a0002c0002t0001g0297a0007c0012t0012g0222 | 2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1714-289T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188491 | ||||||
chr3:149188492
|
A | C | 3 | a0002c0002t0001g0224a0002c0011t0002g0014a0007c0012t0001g0223 | 4 | HG00733.hp2 HG00735.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1714-290T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188492 | ||||||
chr3:149188493
|
A | C | 4 | a0002c0002t0001g0294a0002c0002t0001g0295a0002c0002t0001g0296others(1): Show | 4 | HG01433.hp2 HG02280.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1714-291T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188493 | ||||||
chr3:149188494
|
A | C | 3 | a0002c0002t0001g0298a0002c0002t0002g0301a0002c0002t0002g0338 | 3 | HG02257.hp1 HG02258.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1714-292T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188494 | ||||||
chr3:149188496
|
A | C | 1 | a0002c0006t0002g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1714-294T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188496 | ||||||
chr3:149188497
|
A | C | 19 | a0001c0014t0001g0221a0002c0002t0001g0015a0002c0002t0001g0292others(16): Show | 20 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1714-295T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188497 | ||||||
chr3:149188539
|
T | C | 1 | a0006c0008t0001g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1714-337A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188539 | ||||||
chr3:149188596
|
TG | T | 20 | a0001c0014t0001g0221a0002c0002t0001g0015a0002c0002t0001g0292others(17): Show | 21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1714-395delC | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188596 | ||||||
chr3:149188866
|
A | G | 2 | a0001c0001t0001g0136a0001c0018t0001g0147 | 2 | NA19064.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1714-664T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188866 | ||||||
chr3:149188974
|
T | C | 1 | a0002c0002t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1714-772A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149188974 | ||||||
chr3:149189086
|
G | C | 1 | a0002c0002t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1714-884C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189086 | ||||||
chr3:149189127
|
T | G | 20 | a0001c0014t0001g0221a0002c0002t0001g0015a0002c0002t0001g0292others(17): Show | 21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1714-925A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189127 | ||||||
chr3:149189171
|
A | G | 1 | a0001c0019t0002g0183 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1714-969T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189171 | ||||||
chr3:149189410
|
C | T | 1 | a0006c0008t0006g0340 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1714-1208G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189410 | ||||||
chr3:149189441
|
CT | C | 20 | a0001c0014t0001g0221a0002c0002t0001g0015a0002c0002t0001g0292others(17): Show | 21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1714-1240delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189441 | ||||||
chr3:149189516
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1714-1314A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189516 | ||||||
chr3:149189553
|
C | CA | 10 | a0001c0001t0001g0018a0001c0001t0001g0067a0001c0001t0001g0068others(7): Show | 11 | HG02015.hp1 HG02723.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1714-1352dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189553 | ||||||
chr3:149189553
|
CA | C | 45 | a0001c0001t0001g0019a0001c0001t0001g0206a0001c0001t0001g0333others(42): Show | 49 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1714-1352delT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189553 | ||||||
chr3:149189643
|
C | G | 14 | a0001c0001t0002g0003a0001c0001t0002g0285a0001c0001t0002g0312others(11): Show | 16 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1714-1441G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189643 | ||||||
chr3:149189722
|
G | A | 12 | a0002c0002t0001g0224a0002c0002t0001g0294a0002c0002t0001g0295others(9): Show | 13 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1714-1520C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189722 | ||||||
chr3:149189813
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0010g0237 | 2 | NA18990.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1714-1611T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149189813 | ||||||
chr3:149190208
|
A | G | 12 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(9): Show | 14 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1714-2006T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190208 | ||||||
chr3:149190331
|
C | T | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG03017.hp1 HG03688.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1714-2129G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190331 | ||||||
chr3:149190386
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1714-2184C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190386 | ||||||
chr3:149190605
|
C | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(9): Show | 14 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1714-2403G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190605 | ||||||
chr3:149190656
|
T | TA | 20 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0067others(17): Show | 20 | HG00673.hp1 HG01106.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1714-2455dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190656 | ||||||
chr3:149190656
|
TA | T | 36 | a0001c0001t0001g0019a0001c0001t0001g0141a0001c0001t0001g0242others(33): Show | 39 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1714-2455delT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190656 | ||||||
chr3:149190688
|
G | T | 2 | a0001c0001t0002g0150a0001c0001t0002g0171 | 2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1714-2486C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190688 | ||||||
chr3:149190812
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0239 | 2 | NA18949.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1714-2610T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190812 | ||||||
chr3:149190899
|
A | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0239 | 2 | NA18949.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1714-2697T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190899 | ||||||
chr3:149190921
|
C | T | 1 | a0002c0002t0009g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1714-2719G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149190921 | ||||||
chr3:149191106
|
G | A | 13 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(10): Show | 15 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1714-2904C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191106 | ||||||
chr3:149191167
|
T | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0215 | 2 | HG01168.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1714-2965A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191167 | ||||||
chr3:149191243
|
AT | A | 43 | a0001c0001t0001g0019a0001c0001t0001g0177a0001c0001t0001g0196others(40): Show | 45 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1714-3042delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191243 | ||||||
chr3:149191243
|
ATT | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(113): Show | 127 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.1714-3043_1714-304 others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191243 | ||||||
chr3:149191243
|
ATTT | A | 156 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(153): Show | 163 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1714-3044_1714-304 others(7): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191243 | ||||||
chr3:149191243
|
ATTTT | A | 16 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0102others(13): Show | 16 | HG00738.hp2 HG01106.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1714-3045_1714-304 others(8): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191243 | ||||||
chr3:149191511
|
A | G | 12 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(9): Show | 14 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1714-3309T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191511 | ||||||
chr3:149191550
|
T | TAAGATCA others(300): Show |
9 | a0001c0014t0001g0221a0002c0002t0001g0300a0002c0002t0002g0275others(6): Show | 9 | HG02622.hp2 HG02717.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.1714-3349_1714-334 others(311): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191550 | ||||||
chr3:149191550
|
T | TAAGATCA others(301): Show |
9 | a0002c0002t0001g0015a0002c0002t0001g0292a0002c0002t0001g0303others(6): Show | 10 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1714-3349_1714-334 others(312): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191550 | ||||||
chr3:149191550
|
T | TAAGATCA others(302): Show |
2 | a0002c0002t0003g0288a0002c0002t0003g0290 | 2 | HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1714-3349_1714-334 others(313): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149191550 | ||||||
chr3:149192340
|
T | C | 2 | a0001c0001t0003g0253a0001c0001t0003g0254 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1714-4138A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192340 | ||||||
chr3:149192374
|
C | T | 32 | a0001c0014t0001g0221a0002c0002t0001g0015a0002c0002t0001g0224others(29): Show | 34 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.1714-4172G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192374 | ||||||
chr3:149192484
|
T | C | 1 | a0016c0015t0009g0314 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1714-4282A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192484 | ||||||
chr3:149192493
|
C | CA | 162 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(159): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1714-4292dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192493 | ||||||
chr3:149192670
|
T | TAC | 20 | a0001c0014t0001g0221a0002c0002t0001g0015a0002c0002t0001g0292others(17): Show | 21 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1714-4470_1714-446 others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192670 | ||||||
chr3:149192682
|
CAT | C | 12 | a0002c0002t0001g0224a0002c0002t0001g0294a0002c0002t0001g0295others(9): Show | 13 | HG00733.hp2 HG00735.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1714-4482_1714-448 others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192682 | ||||||
chr3:149192683
|
A | G | 2 | a0001c0001t0001g0069a0001c0021t0001g0133 | 2 | HG00408.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.1714-4481T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192683 | ||||||
chr3:149192684
|
T | C | 1 | a0001c0014t0001g0221 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1714-4482A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192684 | ||||||
chr3:149192685
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1714-4483T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192685 | ||||||
chr3:149192734
|
A | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(141): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1714-4532T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192734 | ||||||
chr3:149192939
|
T | C | 12 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(9): Show | 14 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1714-4737A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192939 | ||||||
chr3:149192981
|
T | TAC | 255 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(252): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.1714-4781_1714-478 others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192981 | ||||||
chr3:149192981
|
T | TACAC | 27 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0037others(24): Show | 27 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.1714-4783_1714-478 others(8): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192981 | ||||||
chr3:149192981
|
TAC | T | 35 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(32): Show | 38 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1714-4781_1714-478 others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149192981 | ||||||
chr3:149193391
|
G | T | 32 | a0001c0014t0001g0221a0002c0002t0001g0015a0002c0002t0001g0224others(29): Show | 34 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.1713+4976C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193391 | ||||||
chr3:149193466
|
G | T | 44 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(41): Show | 48 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1713+4901C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193466 | ||||||
chr3:149193528
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1713+4839C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193528 | ||||||
chr3:149193566
|
T | G | 26 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(23): Show | 30 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1713+4801A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193566 | ||||||
chr3:149193612
|
T | A | 31 | a0002c0002t0001g0015a0002c0002t0001g0224a0002c0002t0001g0292others(28): Show | 33 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1713+4755A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193612 | ||||||
chr3:149193638
|
A | G | 31 | a0002c0002t0001g0015a0002c0002t0001g0224a0002c0002t0001g0292others(28): Show | 33 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1713+4729T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193638 | ||||||
chr3:149193641
|
T | G | 1 | a0001c0001t0002g0171 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1713+4726A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193641 | ||||||
chr3:149193643
|
G | C | 31 | a0002c0002t0001g0015a0002c0002t0001g0224a0002c0002t0001g0292others(28): Show | 33 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1713+4724C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193643 | ||||||
chr3:149193755
|
C | T | 1 | a0001c0001t0006g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1713+4612G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149193755 | ||||||
chr3:149194160
|
G | C | 3 | a0001c0001t0001g0245a0001c0001t0001g0268a0015c0024t0001g0257 | 3 | HG01081.hp1 HG01175.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1713+4207C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194160 | ||||||
chr3:149194197
|
C | CT | 21 | a0001c0010t0001g0225a0001c0010t0001g0226a0002c0002t0001g0015others(18): Show | 22 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1713+4169dupA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194197 | ||||||
chr3:149194245
|
A | AT | 9 | a0001c0001t0001g0235a0001c0001t0001g0242a0001c0001t0001g0243others(6): Show | 9 | HG00738.hp1 HG01099.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1713+4121dupA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194245 | ||||||
chr3:149194245
|
A | T | 1 | a0009c0026t0001g0162 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1713+4122T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194245 | ||||||
chr3:149194245
|
AT | A | 52 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(49): Show | 56 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.1713+4121delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194245 | ||||||
chr3:149194282
|
A | AG | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1713+4084dupC | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194282 | ||||||
chr3:149194352
|
C | T | 29 | a0002c0002t0001g0015a0002c0002t0001g0292a0002c0002t0001g0300others(26): Show | 30 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1713+4015G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194352 | ||||||
chr3:149194427
|
C | T | 1 | a0002c0002t0001g0317 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1713+3940G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194427 | ||||||
chr3:149194581
|
G | A | 1 | a0001c0014t0001g0221 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1713+3786C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194581 | ||||||
chr3:149194607
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0062 | 2 | NA18998.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1713+3760C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194607 | ||||||
chr3:149194614
|
T | TA | 272 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1713+3752dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194614 | ||||||
chr3:149194878
|
A | G | 1 | a0002c0002t0009g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1713+3489T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194878 | ||||||
chr3:149194980
|
T | C | 2 | a0001c0010t0001g0225a0001c0010t0001g0226 | 2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1713+3387A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194980 | ||||||
chr3:149194995
|
T | C | 3 | a0001c0001t0001g0339a0006c0008t0006g0220a0006c0008t0006g0340 | 3 | HG02055.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1713+3372A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149194995 | ||||||
chr3:149195035
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1713+3332C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195035 | ||||||
chr3:149195117
|
G | A | 28 | a0001c0014t0001g0221a0002c0002t0001g0292a0002c0002t0001g0300others(25): Show | 28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+3250C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195117 | ||||||
chr3:149195137
|
A | C | 1 | a0003c0004t0002g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1713+3230T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195137 | ||||||
chr3:149195178
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1713+3189A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195178 | ||||||
chr3:149195209
|
G | A | 323 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(320): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.1713+3158C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195209 | ||||||
chr3:149195239
|
C | A | 28 | a0001c0014t0001g0221a0002c0002t0001g0292a0002c0002t0001g0300others(25): Show | 28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+3128G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195239 | ||||||
chr3:149195268
|
A | T | 28 | a0001c0014t0001g0221a0002c0002t0001g0292a0002c0002t0001g0300others(25): Show | 28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+3099T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195268 | ||||||
chr3:149195339
|
G | T | 51 | a0001c0001t0001g0019a0001c0001t0001g0333a0001c0001t0001g0335others(48): Show | 54 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1713+3028C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195339 | ||||||
chr3:149195535
|
A | G | 3 | a0001c0001t0001g0339a0006c0008t0006g0220a0006c0008t0006g0340 | 3 | HG02055.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1713+2832T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195535 | ||||||
chr3:149195564
|
G | A | 1 | a0001c0001t0002g0312 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1713+2803C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195564 | ||||||
chr3:149195639
|
C | T | 16 | a0001c0001t0001g0018a0001c0001t0001g0330a0001c0001t0001g0331others(13): Show | 19 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1713+2728G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195639 | ||||||
chr3:149195640
|
G | A | 4 | a0002c0002t0001g0298a0002c0002t0001g0299a0002c0002t0002g0301others(1): Show | 4 | HG02257.hp1 HG02258.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1713+2727C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195640 | ||||||
chr3:149195649
|
G | C | 2 | a0001c0001t0001g0064a0001c0001t0002g0063 | 2 | HG00408.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1713+2718C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195649 | ||||||
chr3:149195707
|
C | T | 28 | a0001c0014t0001g0221a0002c0002t0001g0292a0002c0002t0001g0300others(25): Show | 28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+2660G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195707 | ||||||
chr3:149195734
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1713+2633G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195734 | ||||||
chr3:149195797
|
T | C | 29 | a0001c0014t0001g0221a0002c0002t0001g0292a0002c0002t0001g0300others(26): Show | 29 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1713+2570A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195797 | ||||||
chr3:149195858
|
A | G | 28 | a0001c0014t0001g0221a0002c0002t0001g0292a0002c0002t0001g0300others(25): Show | 28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+2509T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195858 | ||||||
chr3:149195861
|
G | A | 28 | a0001c0014t0001g0221a0002c0002t0001g0292a0002c0002t0001g0300others(25): Show | 28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+2506C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149195861 | ||||||
chr3:149196129
|
T | C | 1 | a0003c0004t0002g0231 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1713+2238A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196129 | ||||||
chr3:149196192
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1713+2175A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196192 | ||||||
chr3:149196224
|
C | T | 29 | a0001c0001t0001g0104a0001c0014t0001g0221a0002c0002t0001g0292others(26): Show | 29 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1713+2143G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196224 | ||||||
chr3:149196277
|
T | C | 1 | a0002c0002t0009g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1713+2090A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196277 | ||||||
chr3:149196333
|
A | G | 2 | a0007c0012t0001g0223a0007c0012t0012g0222 | 2 | HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1713+2034T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196333 | ||||||
chr3:149196340
|
T | C | 1 | a0001c0001t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1713+2027A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196340 | ||||||
chr3:149196467
|
C | CA | 9 | a0001c0014t0001g0221a0003c0004t0001g0229a0003c0004t0001g0308others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1713+1899dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196467 | ||||||
chr3:149196530
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1713+1837G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196530 | ||||||
chr3:149196702
|
G | A | 2 | a0001c0010t0001g0225a0001c0010t0001g0226 | 2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1713+1665C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196702 | ||||||
chr3:149196737
|
T | TA | 271 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1713+1629dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196737 | ||||||
chr3:149196756
|
C | T | 14 | a0001c0001t0001g0020a0001c0001t0001g0339a0001c0001t0001g0343others(11): Show | 15 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1713+1611G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196756 | ||||||
chr3:149196769
|
G | GA | 337 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(334): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.1713+1597dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196769 | ||||||
chr3:149196861
|
T | C | 27 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0188others(24): Show | 27 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1713+1506A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196861 | ||||||
chr3:149196916
|
C | T | 3 | a0003c0004t0001g0308a0003c0004t0001g0309a0003c0004t0001g0310 | 3 | HG01167.hp2 HG01169.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1713+1451G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196916 | ||||||
chr3:149196966
|
C | T | 28 | a0001c0014t0001g0221a0002c0002t0001g0292a0002c0002t0001g0300others(25): Show | 28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+1401G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149196966 | ||||||
chr3:149197009
|
C | T | 22 | a0001c0001t0001g0020a0001c0001t0001g0343a0001c0001t0001g0345others(19): Show | 23 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1713+1358G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197009 | ||||||
chr3:149197025
|
G | A | 39 | a0001c0001t0001g0020a0001c0001t0001g0343a0001c0001t0001g0345others(36): Show | 40 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.1713+1342C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197025 | ||||||
chr3:149197034
|
G | T | 39 | a0001c0001t0001g0020a0001c0001t0001g0343a0001c0001t0001g0345others(36): Show | 40 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.1713+1333C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197034 | ||||||
chr3:149197133
|
G | A | 11 | a0001c0014t0001g0221a0003c0004t0001g0229a0003c0004t0001g0308others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1713+1234C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197133 | ||||||
chr3:149197141
|
A | C | 28 | a0001c0014t0001g0221a0002c0002t0001g0292a0002c0002t0001g0300others(25): Show | 28 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1713+1226T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197141 | ||||||
chr3:149197154
|
C | T | 1 | a0002c0002t0001g0294 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1713+1213G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197154 | ||||||
chr3:149197170
|
G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0155a0001c0001t0001g0158 | 3 | HG02040.hp2 NA18986.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1713+1197C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197170 | ||||||
chr3:149197181
|
G | A | 1 | a0007c0012t0012g0222 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1713+1186C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197181 | ||||||
chr3:149197247
|
T | C | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG00642.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1713+1120A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197247 | ||||||
chr3:149197253
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG00642.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1713+1114G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197253 | ||||||
chr3:149197364
|
G | A | 1 | a0002c0002t0009g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1713+1003C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197364 | ||||||
chr3:149197375
|
A | G | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(25): Show | 33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1713+992T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197375 | ||||||
chr3:149197384
|
A | T | 1 | a0001c0001t0001g0167 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1713+983T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197384 | ||||||
chr3:149197513
|
G | GA | 17 | a0001c0001t0001g0020a0001c0001t0001g0339a0001c0001t0001g0343others(14): Show | 18 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1713+853dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197513 | ||||||
chr3:149197513
|
G | GAA | 29 | a0001c0014t0001g0221a0002c0002t0001g0292a0002c0002t0001g0293others(26): Show | 29 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1713+852_1713+853d others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197513 | ||||||
chr3:149197657
|
C | A | 1 | a0001c0001t0001g0160 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1713+710G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197657 | ||||||
chr3:149197787
|
T | A | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(25): Show | 33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1713+580A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197787 | ||||||
chr3:149197798
|
G | A | 12 | a0001c0014t0001g0221a0002c0002t0009g0093a0003c0004t0001g0229others(9): Show | 12 | HG01167.hp2 HG01169.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1713+569C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197798 | ||||||
chr3:149197835
|
A | C | 11 | a0001c0014t0001g0221a0003c0004t0001g0229a0003c0004t0001g0308others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1713+532T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197835 | ||||||
chr3:149197841
|
T | C | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(25): Show | 33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1713+526A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197841 | ||||||
chr3:149197934
|
T | G | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(66): Show | 73 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.1713+433A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197934 | ||||||
chr3:149197959
|
C | T | 11 | a0001c0014t0001g0221a0003c0004t0001g0229a0003c0004t0001g0308others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1713+408G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149197959 | ||||||
chr3:149198046
|
G | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0343a0001c0001t0001g0345others(5): Show | 9 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1713+321C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149198046 | ||||||
chr3:149198212
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1713+155C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 9/18 | chr3 | 149198212 | ||||||
chr3:149198939
|
A | T | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1502-361T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 8/18 | chr3 | 149198939 | ||||||
chr3:149199209
|
C | A | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1501+503G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 8/18 | chr3 | 149199209 | ||||||
chr3:149199217
|
G | A | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1501+495C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 8/18 | chr3 | 149199217 | ||||||
chr3:149199259
|
C | T | 36 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(33): Show | 41 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1501+453G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 8/18 | chr3 | 149199259 | ||||||
chr3:149199330
|
C | T | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1501+382G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 8/18 | chr3 | 149199330 | ||||||
chr3:149199425
|
T | G | 1 | a0001c0001t0001g0033 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1501+287A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 8/18 | chr3 | 149199425 | ||||||
chr3:149199877
|
A | G | 11 | a0001c0001t0001g0103a0001c0001t0001g0109a0001c0001t0001g0119others(8): Show | 11 | HG00408.hp2 HG01258.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1349-13T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149199877 | ||||||
chr3:149199960
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1349-96G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149199960 | ||||||
chr3:149200057
|
G | C | 3 | a0001c0001t0001g0339a0006c0008t0006g0220a0006c0008t0006g0340 | 3 | HG02055.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1349-193C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149200057 | ||||||
chr3:149200215
|
G | A | 1 | a0002c0002t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1349-351C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149200215 | ||||||
chr3:149200499
|
C | A | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1349-635G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149200499 | ||||||
chr3:149200554
|
G | A | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(25): Show | 33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1349-690C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149200554 | ||||||
chr3:149200858
|
C | A | 1 | a0001c0001t0002g0157 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1349-994G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149200858 | ||||||
chr3:149200953
|
A | G | 1 | a0007c0012t0001g0223 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1349-1089T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149200953 | ||||||
chr3:149201016
|
G | A | 2 | a0002c0002t0001g0224a0002c0002t0001g0297 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1348+1086C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201016 | ||||||
chr3:149201107
|
G | GGATT | 20 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0050others(17): Show | 21 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1348+991_1348+994d others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201107 | ||||||
chr3:149201107
|
GGATT | G | 6 | a0003c0004t0001g0229a0003c0004t0001g0310a0003c0004t0001g0311others(3): Show | 6 | HG02615.hp1 HG02630.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1348+991_1348+994d others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201107 | ||||||
chr3:149201107
|
GGATTGAT others(1): Show |
G | 5 | a0002c0002t0001g0294a0002c0002t0001g0295a0002c0002t0001g0296others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1348+987_1348+994d others(10): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201107 | ||||||
chr3:149201134
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1348+968A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201134 | ||||||
chr3:149201157
|
T | A | 22 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(19): Show | 26 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1348+945A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201157 | ||||||
chr3:149201186
|
A | T | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1348+916T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201186 | ||||||
chr3:149201217
|
G | A | 1 | a0001c0001t0004g0161 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1348+885C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201217 | ||||||
chr3:149201322
|
C | T | 1 | a0004c0009t0001g0078 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1348+780G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201322 | ||||||
chr3:149201430
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1348+672C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201430 | ||||||
chr3:149201452
|
TCTTTAA | T | 4 | a0001c0001t0001g0343a0001c0001t0001g0345a0001c0001t0001g0349others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348+644_1348+649d others(8): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201452 | ||||||
chr3:149201783
|
A | G | 1 | a0012c0017t0007g0306 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1348+319T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201783 | ||||||
chr3:149201827
|
C | T | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1348+275G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201827 | ||||||
chr3:149201891
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0159 | 2 | NA18968.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1348+211C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149201891 | ||||||
chr3:149202047
|
T | C | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1348+55A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149202047 | ||||||
chr3:149202093
|
A | G | 2 | a0001c0010t0001g0225a0001c0010t0001g0226 | 2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1348+9T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 7/18 | chr3 | 149202093 | ||||||
chr3:149202256
|
A | T | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-15T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202256 | ||||||
chr3:149202431
|
C | A | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-190G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202431 | ||||||
chr3:149202534
|
A | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0273 | 3 | NA18960.hp2 NA18975.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1209-293T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202534 | ||||||
chr3:149202562
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1209-321T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202562 | ||||||
chr3:149202605
|
C | CT | 25 | a0001c0001t0001g0030a0001c0001t0001g0047a0001c0001t0001g0048others(22): Show | 28 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1209-365dupA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202605 | ||||||
chr3:149202605
|
CT | C | 116 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(113): Show | 121 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1209-365delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202605 | ||||||
chr3:149202605
|
CTT | C | 12 | a0001c0001t0001g0160a0001c0001t0001g0186a0001c0001t0001g0205others(9): Show | 12 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.1209-366_1209-365d others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202605 | ||||||
chr3:149202701
|
G | A | 1 | a0002c0002t0009g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1209-460C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202701 | ||||||
chr3:149202711
|
C | T | 5 | a0001c0003t0001g0008a0001c0003t0001g0088a0001c0003t0001g0089others(2): Show | 6 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-470G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202711 | ||||||
chr3:149202753
|
G | A | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-512C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202753 | ||||||
chr3:149202811
|
A | G | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-570T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202811 | ||||||
chr3:149202908
|
C | CT | 43 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0030others(40): Show | 48 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.1209-668dupA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202908 | ||||||
chr3:149202908
|
CT | C | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-668delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202908 | ||||||
chr3:149202938
|
A | G | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-697T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202938 | ||||||
chr3:149202947
|
C | A | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-706G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202947 | ||||||
chr3:149202959
|
T | G | 1 | a0002c0002t0001g0292 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1209-718A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202959 | ||||||
chr3:149202998
|
T | C | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-757A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149202998 | ||||||
chr3:149203064
|
G | A | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-823C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203064 | ||||||
chr3:149203087
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1209-846A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203087 | ||||||
chr3:149203107
|
C | T | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-866G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203107 | ||||||
chr3:149203155
|
T | C | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-914A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203155 | ||||||
chr3:149203187
|
G | A | 3 | a0001c0014t0001g0221a0007c0012t0001g0223a0007c0012t0012g0222 | 3 | HG02572.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1209-946C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203187 | ||||||
chr3:149203196
|
T | C | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(25): Show | 33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1209-955A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203196 | ||||||
chr3:149203202
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | NA18959.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1209-961G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203202 | ||||||
chr3:149203216
|
A | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(138): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1209-975T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203216 | ||||||
chr3:149203306
|
CA | C | 37 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0194others(34): Show | 41 | HG00738.hp1 HG01069.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.1209-1066delT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203306 | ||||||
chr3:149203345
|
A | C | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-1104T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203345 | ||||||
chr3:149203348
|
C | A | 4 | a0004c0009t0001g0078a0004c0009t0001g0260a0004c0009t0001g0269others(1): Show | 5 | HG01192.hp1 HG02273.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209-1107G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203348 | ||||||
chr3:149203556
|
G | T | 1 | a0002c0002t0001g0294 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1209-1315C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203556 | ||||||
chr3:149203558
|
T | C | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-1317A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203558 | ||||||
chr3:149203638
|
C | T | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-1397G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203638 | ||||||
chr3:149203702
|
C | A | 1 | a0001c0001t0001g0191 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1209-1461G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203702 | ||||||
chr3:149203839
|
C | T | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-1598G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203839 | ||||||
chr3:149203982
|
G | C | 1 | a0002c0002t0009g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1209-1741C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203982 | ||||||
chr3:149203987
|
AGT | A | 3 | a0005c0007t0005g0307a0005c0007t0005g0315a0005c0007t0005g0316 | 3 | HG03195.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1209-1748_1209-174 others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149203987 | ||||||
chr3:149204017
|
G | A | 1 | a0002c0002t0009g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1209-1776C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204017 | ||||||
chr3:149204021
|
A | C | 1 | a0001c0001t0001g0114 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1209-1780T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204021 | ||||||
chr3:149204031
|
G | C | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-1790C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204031 | ||||||
chr3:149204056
|
G | A | 70 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(67): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1209-1815C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204056 | ||||||
chr3:149204061
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1209-1820C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204061 | ||||||
chr3:149204065
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG00735.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1209-1824C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204065 | ||||||
chr3:149204098
|
C | T | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1209-1857G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204098 | ||||||
chr3:149204161
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1209-1920A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204161 | ||||||
chr3:149204259
|
G | A | 16 | a0001c0001t0001g0018a0001c0001t0001g0330a0001c0001t0001g0331others(13): Show | 19 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1208+1909C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204259 | ||||||
chr3:149204530
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1208+1638G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149204530 | ||||||
chr3:149205001
|
T | TCAA | 22 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(19): Show | 26 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1208+1164_1208+116 others(7): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205001 | ||||||
chr3:149205001
|
T | TCAACAA | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208+1161_1208+116 others(10): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205001 | ||||||
chr3:149205090
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1208+1078T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205090 | ||||||
chr3:149205143
|
C | A | 336 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(333): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.1208+1025G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205143 | ||||||
chr3:149205230
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1208+938T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205230 | ||||||
chr3:149205295
|
G | A | 8 | a0003c0004t0001g0229a0003c0004t0001g0308a0003c0004t0001g0309others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1208+873C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205295 | ||||||
chr3:149205374
|
G | C | 4 | a0001c0001t0001g0343a0001c0001t0001g0345a0001c0001t0001g0349others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208+794C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205374 | ||||||
chr3:149205380
|
G | T | 1 | a0001c0001t0003g0233 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1208+788C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205380 | ||||||
chr3:149205500
|
A | T | 3 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113 | 3 | HG00438.hp1 HG00558.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1208+668T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205500 | ||||||
chr3:149205612
|
A | T | 1 | a0001c0001t0002g0329 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1208+556T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205612 | ||||||
chr3:149205753
|
G | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0346a0001c0001t0001g0347others(1): Show | 5 | HG01243.hp2 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208+415C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205753 | ||||||
chr3:149205754
|
T | C | 1 | a0002c0002t0003g0289 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1208+414A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205754 | ||||||
chr3:149205869
|
G | A | 43 | a0001c0001t0001g0172a0001c0001t0001g0181a0001c0001t0001g0194others(40): Show | 47 | HG00323.hp1 HG00738.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1208+299C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 6/18 | chr3 | 149205869 | ||||||
chr3:149206390
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1037-51A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149206390 | ||||||
chr3:149206414
|
C | T | 4 | a0001c0001t0001g0232a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | NA18980.hp2 NA18989.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1037-75G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149206414 | ||||||
chr3:149206443
|
T | C | 15 | a0001c0001t0001g0020a0001c0001t0001g0339a0001c0001t0001g0343others(12): Show | 16 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1037-104A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149206443 | ||||||
chr3:149206590
|
C | T | 1 | a0009c0026t0001g0162 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1037-251G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149206590 | ||||||
chr3:149206818
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1037-479C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149206818 | ||||||
chr3:149206852
|
A | G | 1 | a0001c0001t0001g0080 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1036+511T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149206852 | ||||||
chr3:149206979
|
G | A | 4 | a0002c0002t0001g0298a0002c0002t0001g0299a0002c0002t0002g0301others(1): Show | 4 | HG02257.hp1 HG02258.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+384C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149206979 | ||||||
chr3:149207047
|
T | C | 34 | a0002c0002t0001g0292a0002c0002t0001g0293a0002c0002t0001g0294others(31): Show | 35 | HG00733.hp2 HG00735.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.1036+316A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 5/18 | chr3 | 149207047 | ||||||
chr3:149207631
|
G | A | 22 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(19): Show | 26 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.782-14C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149207631 | ||||||
chr3:149207738
|
T | C | 337 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(334): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.782-121A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149207738 | ||||||
chr3:149207744
|
C | T | 1 | a0001c0001t0001g0341 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.782-127G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149207744 | ||||||
chr3:149207779
|
G | A | 22 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(19): Show | 26 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.782-162C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149207779 | ||||||
chr3:149207865
|
C | A | 3 | a0001c0001t0001g0339a0006c0008t0006g0220a0006c0008t0006g0340 | 3 | HG02055.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.782-248G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149207865 | ||||||
chr3:149207977
|
T | C | 9 | a0001c0001t0001g0020a0001c0001t0001g0343a0001c0001t0001g0345others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.782-360A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149207977 | ||||||
chr3:149208022
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.782-405C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208022 | ||||||
chr3:149208276
|
C | G | 6 | a0001c0001t0001g0339a0005c0007t0005g0307a0005c0007t0005g0315others(3): Show | 6 | HG02055.hp2 HG02615.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.782-659G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208276 | ||||||
chr3:149208329
|
T | A | 28 | a0002c0002t0001g0224a0002c0002t0001g0292a0002c0002t0001g0293others(25): Show | 29 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.782-712A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208329 | ||||||
chr3:149208347
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.782-730G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208347 | ||||||
chr3:149208377
|
C | G | 1 | a0001c0001t0001g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.782-760G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208377 | ||||||
chr3:149208438
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.781+773G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208438 | ||||||
chr3:149208443
|
T | C | 26 | a0002c0002t0001g0292a0002c0002t0001g0293a0002c0002t0001g0294others(23): Show | 27 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.781+768A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208443 | ||||||
chr3:149208483
|
T | C | 2 | a0001c0010t0001g0225a0001c0010t0001g0226 | 2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.781+728A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208483 | ||||||
chr3:149208489
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.781+722T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208489 | ||||||
chr3:149208528
|
G | A | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(25): Show | 33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.781+683C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208528 | ||||||
chr3:149208564
|
A | G | 1 | a0001c0001t0001g0246 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.781+647T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208564 | ||||||
chr3:149208569
|
CAAAT | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0273 | 3 | NA18960.hp2 NA18975.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.781+638_781+641del others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208569 | ||||||
chr3:149208817
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.781+394C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 4/18 | chr3 | 149208817 | ||||||
chr3:149209716
|
C | G | 6 | a0001c0003t0001g0008a0001c0003t0001g0088a0001c0003t0001g0089others(3): Show | 7 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.608-332G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149209716 | ||||||
chr3:149209924
|
A | T | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(25): Show | 33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.607+243T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149209924 | ||||||
chr3:149209937
|
A | T | 6 | a0001c0001t0001g0339a0005c0007t0005g0307a0005c0007t0005g0315others(3): Show | 6 | HG02055.hp2 HG02615.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.607+230T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149209937 | ||||||
chr3:149209992
|
T | G | 1 | a0001c0001t0001g0339 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.607+175A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149209992 | ||||||
chr3:149210028
|
C | T | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(25): Show | 33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.607+139G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149210028 | ||||||
chr3:149210038
|
T | C | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(25): Show | 33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.607+129A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149210038 | ||||||
chr3:149210059
|
C | T | 2 | a0003c0004t0001g0308a0003c0004t0001g0309 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.607+108G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149210059 | ||||||
chr3:149210062
|
T | C | 1 | a0005c0007t0005g0316 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.607+105A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149210062 | ||||||
chr3:149210065
|
C | T | 1 | a0001c0001t0002g0163 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.607+102G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149210065 | ||||||
chr3:149210106
|
G | A | 2 | a0001c0001t0002g0163a0011c0020t0002g0164 | 2 | NA18962.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.607+61C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149210106 | ||||||
chr3:149210138
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.607+29T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 3/18 | chr3 | 149210138 | ||||||
chr3:149210506
|
T | A | 28 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0330others(25): Show | 33 | HG00673.hp2 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.395-127A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149210506 | ||||||
chr3:149210752
|
T | C | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.395-373A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149210752 | ||||||
chr3:149210758
|
C | T | 1 | a0001c0001t0006g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.395-379G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149210758 | ||||||
chr3:149210869
|
G | C | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG03490.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.395-490C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149210869 | ||||||
chr3:149211136
|
A | G | 5 | a0001c0003t0001g0008a0001c0003t0001g0088a0001c0003t0001g0089others(2): Show | 6 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.395-757T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149211136 | ||||||
chr3:149211148
|
A | C | 2 | a0001c0010t0001g0225a0001c0010t0001g0226 | 2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.395-769T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149211148 | ||||||
chr3:149211353
|
G | T | 1 | a0002c0002t0003g0290 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.395-974C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149211353 | ||||||
chr3:149211591
|
T | C | 2 | a0001c0010t0001g0225a0001c0010t0001g0226 | 2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.394+860A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149211591 | ||||||
chr3:149211618
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.394+833G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149211618 | ||||||
chr3:149211725
|
A | G | 16 | a0001c0001t0001g0018a0001c0001t0001g0330a0001c0001t0001g0331others(13): Show | 19 | HG00673.hp2 HG01070.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.394+726T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149211725 | ||||||
chr3:149211818
|
G | C | 1 | a0001c0001t0001g0067 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.394+633C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149211818 | ||||||
chr3:149212011
|
T | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(193): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.394+440A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212011 | ||||||
chr3:149212013
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.394+438C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212013 | ||||||
chr3:149212024
|
T | A | 3 | a0005c0007t0005g0307a0005c0007t0005g0315a0005c0007t0005g0316 | 3 | HG03195.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.394+427A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212024 | ||||||
chr3:149212032
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.394+419C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212032 | ||||||
chr3:149212064
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.394+387G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212064 | ||||||
chr3:149212121
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.394+330C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212121 | ||||||
chr3:149212123
|
C | G | 1 | a0001c0001t0001g0235 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.394+328G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212123 | ||||||
chr3:149212130
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.394+321T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212130 | ||||||
chr3:149212135
|
T | C | 22 | a0002c0002t0001g0292a0002c0002t0001g0293a0002c0002t0001g0294others(19): Show | 23 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.394+316A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212135 | ||||||
chr3:149212164
|
T | A | 100 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(97): Show | 109 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.394+287A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212164 | ||||||
chr3:149212267
|
T | C | 351 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(348): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.394+184A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212267 | ||||||
chr3:149212290
|
G | A | 25 | a0002c0002t0001g0292a0002c0002t0001g0294a0002c0002t0001g0295others(22): Show | 26 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.394+161C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212290 | ||||||
chr3:149212292
|
C | A | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(66): Show | 73 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.394+159G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212292 | ||||||
chr3:149212309
|
T | A | 70 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(67): Show | 75 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.394+142A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212309 | ||||||
chr3:149212310
|
A | T | 5 | a0002c0002t0001g0297a0003c0004t0001g0229a0003c0004t0002g0228others(2): Show | 5 | HG02630.hp1 HG02922.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+141T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212310 | ||||||
chr3:149212326
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.394+125T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212326 | ||||||
chr3:149212381
|
A | C | 1 | a0001c0001t0001g0004 | 2 | NA18975.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.394+70T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212381 | ||||||
chr3:149212431
|
G | A | 68 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(65): Show | 72 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.394+20C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 2/18 | chr3 | 149212431 | ||||||
chr3:149212952
|
C | G | 1 | a0001c0001t0001g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.147-254G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149212952 | ||||||
chr3:149213120
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0346others(2): Show | 7 | HG01243.hp2 HG02559.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-422T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213120 | ||||||
chr3:149213211
|
A | T | 68 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(65): Show | 72 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.147-513T>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213211 | ||||||
chr3:149213212
|
T | A | 68 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(65): Show | 72 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.147-514A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213212 | ||||||
chr3:149213269
|
G | T | 1 | a0001c0001t0006g0284 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147-571C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213269 | ||||||
chr3:149213318
|
C | T | 8 | a0001c0001t0001g0020a0001c0001t0001g0345a0001c0001t0001g0346others(5): Show | 9 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.147-620G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213318 | ||||||
chr3:149213354
|
T | C | 8 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(5): Show | 8 | HG00597.hp2 HG01433.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.147-656A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213354 | ||||||
chr3:149213524
|
G | T | 1 | a0002c0002t0001g0292 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.147-826C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213524 | ||||||
chr3:149213630
|
GGGTGT | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0347a0002c0002t0002g0276 | 3 | HG01243.hp2 NA18990.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.147-937_147-933del others(5): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213630 | ||||||
chr3:149213631
|
G | GGT | 13 | a0001c0001t0001g0343a0001c0001t0002g0312a0001c0001t0006g0284others(10): Show | 13 | HG01167.hp2 HG01169.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.147-935_147-934dup others(2): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | ||||||
chr3:149213631
|
GGT | G | 24 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0103others(21): Show | 26 | HG00738.hp1 HG02257.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.147-935_147-934del others(2): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | ||||||
chr3:149213631
|
GGTGT | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(132): Show | 141 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.147-937_147-934del others(4): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | ||||||
chr3:149213631
|
GGTGTGT | G | 62 | a0001c0001t0001g0013a0001c0001t0001g0167a0001c0001t0001g0168others(59): Show | 69 | HG00323.hp1 HG00558.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.147-939_147-934del others(6): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | ||||||
chr3:149213631
|
GGTGTGTG others(1): Show |
G | 5 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0268others(2): Show | 5 | HG00642.hp2 HG01175.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-941_147-934del others(8): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | ||||||
chr3:149213631
|
GGTGTGTG others(3): Show |
G | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG00099.hp2 HG01070.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-943_147-934del others(10): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | ||||||
chr3:149213631
|
GGTGTGTG others(5): Show |
G | 1 | a0001c0001t0001g0029 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.147-945_147-934del others(12): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | ||||||
chr3:149213631
|
GGTGTGTG others(7): Show |
G | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(66): Show | 73 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.147-947_147-934del others(14): Show |
CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213631 | ||||||
chr3:149213737
|
G | T | 70 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(67): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.147-1039C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213737 | ||||||
chr3:149213739
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.147-1041C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213739 | ||||||
chr3:149213977
|
G | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0345a0001c0001t0001g0346others(5): Show | 9 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.147-1279C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149213977 | ||||||
chr3:149214003
|
T | C | 3 | a0001c0001t0003g0270a0001c0001t0003g0271a0001c0001t0003g0272 | 3 | HG00738.hp1 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.147-1305A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214003 | ||||||
chr3:149214022
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.147-1324G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214022 | ||||||
chr3:149214029
|
T | A | 1 | a0002c0002t0003g0291 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.147-1331A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214029 | ||||||
chr3:149214053
|
G | C | 1 | a0001c0001t0001g0176 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.147-1355C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214053 | ||||||
chr3:149214171
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.147-1473C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214171 | ||||||
chr3:149214193
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(126): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.147-1495C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214193 | ||||||
chr3:149214242
|
T | C | 1 | a0001c0001t0002g0337 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.147-1544A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214242 | ||||||
chr3:149214298
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0003g0178 | 2 | HG01255.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.147-1600C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214298 | ||||||
chr3:149214318
|
G | A | 1 | a0004c0009t0001g0269 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.147-1620C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214318 | ||||||
chr3:149214353
|
T | C | 3 | a0001c0001t0003g0270a0001c0001t0003g0271a0001c0001t0003g0272 | 3 | HG00738.hp1 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.147-1655A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214353 | ||||||
chr3:149214374
|
A | G | 1 | a0001c0001t0003g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.147-1676T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214374 | ||||||
chr3:149214382
|
C | A | 70 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(67): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.147-1684G>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214382 | ||||||
chr3:149214506
|
C | G | 1 | a0001c0001t0001g0099 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.147-1808G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214506 | ||||||
chr3:149214510
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.147-1812A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214510 | ||||||
chr3:149214712
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0273 | 3 | NA18960.hp2 NA18975.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.147-2014C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214712 | ||||||
chr3:149214923
|
T | C | 1 | a0002c0002t0002g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-2225A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214923 | ||||||
chr3:149214967
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.147-2269G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149214967 | ||||||
chr3:149215299
|
T | G | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(66): Show | 73 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.147-2601A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149215299 | ||||||
chr3:149215491
|
T | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0346a0001c0001t0001g0347others(4): Show | 8 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.147-2793A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149215491 | ||||||
chr3:149215626
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.147-2928A>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149215626 | ||||||
chr3:149215765
|
A | G | 1 | a0001c0001t0006g0284 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.147-3067T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149215765 | ||||||
chr3:149215884
|
A | G | 1 | a0012c0017t0007g0306 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.147-3186T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149215884 | ||||||
chr3:149216009
|
C | T | 5 | a0002c0002t0001g0015a0002c0002t0001g0302a0002c0002t0001g0303others(2): Show | 6 | HG02258.hp1 HG02486.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.147-3311G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216009 | ||||||
chr3:149216354
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.147-3656A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216354 | ||||||
chr3:149216423
|
G | A | 1 | a0002c0002t0002g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.147-3725C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216423 | ||||||
chr3:149216443
|
C | T | 33 | a0001c0001t0001g0343a0001c0001t0001g0345a0002c0002t0001g0292others(30): Show | 34 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.147-3745G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216443 | ||||||
chr3:149216615
|
G | A | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 4 | HG03239.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-3917C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216615 | ||||||
chr3:149216811
|
A | C | 6 | a0002c0002t0003g0286a0002c0002t0003g0288a0002c0002t0003g0289others(3): Show | 6 | HG01243.hp1 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.147-4113T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216811 | ||||||
chr3:149216874
|
A | C | 15 | a0001c0001t0001g0345a0002c0002t0001g0292a0002c0002t0001g0293others(12): Show | 16 | HG00733.hp2 HG00735.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.147-4176T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216874 | ||||||
chr3:149216900
|
C | CT | 16 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(13): Show | 16 | HG00733.hp1 HG01074.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.147-4203dupA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216900 | ||||||
chr3:149216900
|
CT | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0187a0001c0001t0001g0188others(8): Show | 11 | HG00323.hp2 HG01069.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.147-4203delA | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216900 | ||||||
chr3:149216954
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.147-4256C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149216954 | ||||||
chr3:149217177
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.146+4470C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217177 | ||||||
chr3:149217445
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.146+4202A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217445 | ||||||
chr3:149217545
|
G | A | 1 | a0006c0008t0006g0220 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.146+4102C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217545 | ||||||
chr3:149217640
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.146+4007A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217640 | ||||||
chr3:149217693
|
T | C | 66 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(63): Show | 70 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.146+3954A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217693 | ||||||
chr3:149217850
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.146+3797A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217850 | ||||||
chr3:149217874
|
G | A | 1 | a0001c0010t0001g0226 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.146+3773C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217874 | ||||||
chr3:149217879
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.146+3768C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149217879 | ||||||
chr3:149218004
|
C | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0346a0001c0001t0001g0347others(4): Show | 8 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.146+3643G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218004 | ||||||
chr3:149218072
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.146+3575T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218072 | ||||||
chr3:149218106
|
A | G | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(66): Show | 73 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.146+3541T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218106 | ||||||
chr3:149218117
|
T | A | 1 | a0001c0001t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.146+3530A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218117 | ||||||
chr3:149218442
|
C | G | 8 | a0002c0002t0002g0275a0002c0002t0002g0276a0002c0002t0002g0281others(5): Show | 8 | HG03098.hp2 HG03139.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.146+3205G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218442 | ||||||
chr3:149218466
|
G | A | 27 | a0001c0001t0001g0011a0001c0001t0001g0192a0001c0001t0001g0193others(24): Show | 28 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.146+3181C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218466 | ||||||
chr3:149218530
|
T | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0011others(129): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.146+3117A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218530 | ||||||
chr3:149218598
|
C | T | 8 | a0002c0002t0002g0275a0002c0002t0002g0276a0002c0002t0002g0281others(5): Show | 8 | HG03098.hp2 HG03139.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.146+3049G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218598 | ||||||
chr3:149218790
|
C | T | 49 | a0001c0001t0001g0013a0001c0001t0001g0219a0001c0001t0001g0232others(46): Show | 54 | HG00323.hp1 HG00738.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.146+2857G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218790 | ||||||
chr3:149218941
|
T | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02074.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.146+2706A>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218941 | ||||||
chr3:149218962
|
A | G | 69 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0007others(66): Show | 73 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.146+2685T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149218962 | ||||||
chr3:149219353
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.146+2294G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149219353 | ||||||
chr3:149219404
|
G | C | 1 | a0001c0001t0001g0217 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.146+2243C>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149219404 | ||||||
chr3:149219444
|
C | T | 4 | a0003c0004t0001g0229a0003c0004t0002g0228a0003c0004t0002g0230others(1): Show | 4 | HG02630.hp1 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.146+2203G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149219444 | ||||||
chr3:149219971
|
C | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0346 | 3 | HG02559.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.146+1676G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149219971 | ||||||
chr3:149220103
|
G | A | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0021others(60): Show | 66 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.146+1544C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220103 | ||||||
chr3:149220131
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | NA19000.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.146+1516G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220131 | ||||||
chr3:149220325
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.146+1322A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220325 | ||||||
chr3:149220354
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.146+1293G>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220354 | ||||||
chr3:149220490
|
T | TA | 351 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(348): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.146+1156dupT | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220490 | ||||||
chr3:149220559
|
T | C | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0021others(58): Show | 64 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.146+1088A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220559 | ||||||
chr3:149220593
|
T | C | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0021others(58): Show | 64 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.146+1054A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220593 | ||||||
chr3:149220705
|
C | T | 6 | a0001c0010t0001g0225a0001c0010t0001g0226a0001c0014t0001g0221others(3): Show | 6 | HG02572.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.146+942G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220705 | ||||||
chr3:149220707
|
G | A | 2 | a0001c0001t0001g0345a0017c0028t0001g0344 | 2 | HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.146+940C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220707 | ||||||
chr3:149220868
|
A | G | 1 | a0006c0008t0006g0220 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.146+779T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220868 | ||||||
chr3:149220891
|
A | C | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0021others(58): Show | 64 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.146+756T>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220891 | ||||||
chr3:149220990
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.146+657T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149220990 | ||||||
chr3:149221163
|
A | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(144): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.146+484T>C | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149221163 | ||||||
chr3:149221350
|
G | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(4): Show | 7 | HG00323.hp2 HG00735.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.146+297C>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149221350 | ||||||
chr3:149221390
|
G | A | 7 | a0001c0001t0001g0020a0001c0001t0001g0346a0001c0001t0001g0347others(4): Show | 8 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.146+257C>T | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149221390 | ||||||
chr3:149221551
|
T | C | 1 | a0001c0001t0001g0352 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.146+96A>G | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149221551 | ||||||
chr3:149221606
|
C | T | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0021others(58): Show | 64 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.146+41G>A | CP | ENSG00000047457.14 | transcript | ENST00000264613.11 | protein_coding | 1/18 | chr3 | 149221606 |