geneid | 133418 |
---|---|
ensemblid | ENSG00000170571.12 |
hgncid | 30465 |
symbol | EMB |
name | embigin |
refseq_nuc | NM_198449.3 |
refseq_prot | NP_940851.1 |
ensembl_nuc | ENST00000303221.10 |
ensembl_prot | ENSP00000302289.5 |
mane_status | MANE Select |
chr | chr5 |
start | 50396192 |
end | 50441288 |
strand | - |
ver | v1.2 |
region | chr5:50396192-50441288 |
region5000 | chr5:50391192-50446288 |
regionname0 | EMB_chr5_50396192_50441288 |
regionname5000 | EMB_chr5_50391192_50446288 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 327 | 340 | 88 | 58 | 140 | 14 | 38 | 104 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0002 | 0/0 | 327 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0003 | 0/0 | 277 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0004 | 0/0 | 327 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0005 | 0/0 | 327 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0006 | 0/0 | 327 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 984 | 319 | 79 | 54 | 132 | 14 | 38 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
c0002 | 0/0 | 984 | 18 | 9 | 2 | 7 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
c0003 | 0/0 | 984 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
c0004 | 0/0 | 984 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
c0005 | 0/0 | 984 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
c0006 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
c0007 | 0/0 | 984 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
c0008 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
c0009 | 0/0 | 984 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3219 | 130 | 22 | 25 | 56 | 8 | 18 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0002 | 0/0 | 3220 | 59 | 7 | 6 | 41 | 1 | 4 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0003 | 0/1 | 3220 | 36 | 6 | 3 | 21 | 1 | 4 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0004 | 0/0 | 3220 | 34 | 20 | 7 | 7 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0005 | 0/0 | 3220 | 24 | 14 | 4 | 0 | 1 | 5 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0006 | 0/0 | 3220 | 15 | 0 | 2 | 10 | 1 | 2 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0007 | 0/0 | 3220 | 12 | 0 | 6 | 0 | 1 | 5 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0008 | 0/0 | 3220 | 5 | 5 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0009 | 0/0 | 3220 | 4 | 4 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0010 | 0/0 | 3220 | 3 | 3 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0011 | 0/0 | 3220 | 3 | 3 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0012 | 0/0 | 3220 | 2 | 1 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0013 | 0/0 | 3220 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0014 | 0/0 | 3220 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0015 | 0/0 | 3219 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0016 | 0/0 | 3220 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0017 | 0/0 | 3219 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0018 | 0/0 | 3219 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0019 | 0/0 | 3219 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0020 | 0/0 | 3219 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0021 | 0/0 | 3219 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0022 | 0/0 | 3219 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0023 | 0/0 | 3219 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0024 | 0/0 | 3219 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0025 | 0/0 | 3220 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0026 | 0/0 | 3220 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0027 | 0/0 | 3220 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0028 | 0/0 | 3220 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
t0029 | 0/0 | 3219 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0025 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 984 | 319 | 79 | 54 | 132 | 14 | 38 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0002 | 0/0 | 984 | 18 | 9 | 2 | 7 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0004 | 0/0 | 984 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0007 | 0/0 | 984 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0002c0003 | 0/0 | 984 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0003c0005 | 0/0 | 984 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0004c0009 | 0/0 | 984 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0005c0008 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0006c0006 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4202 | 128 | 20 | 25 | 56 | 8 | 18 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0002 | 0/0 | 4203 | 56 | 7 | 6 | 38 | 1 | 4 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0003 | 0/1 | 4203 | 36 | 6 | 3 | 21 | 1 | 4 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0004 | 0/0 | 4203 | 17 | 14 | 3 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0005 | 0/0 | 4203 | 24 | 14 | 4 | 0 | 1 | 5 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0006 | 0/0 | 4203 | 14 | 0 | 2 | 9 | 1 | 2 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0007 | 0/0 | 4203 | 12 | 0 | 6 | 0 | 1 | 5 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0008 | 0/0 | 4203 | 5 | 5 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0009 | 0/0 | 4203 | 4 | 4 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0010 | 0/0 | 4203 | 3 | 3 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0012 | 0/0 | 4203 | 2 | 1 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0013 | 0/0 | 4203 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0014 | 0/0 | 4203 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0015 | 0/0 | 4202 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0016 | 0/0 | 4203 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0017 | 0/0 | 4202 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0018 | 0/0 | 4202 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0019 | 0/0 | 4202 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0020 | 0/0 | 4202 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0021 | 0/0 | 4202 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0022 | 0/0 | 4202 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0023 | 0/0 | 4202 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0024 | 0/0 | 4202 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0025 | 0/0 | 4203 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0026 | 0/0 | 4203 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0027 | 0/0 | 4203 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0001t0028 | 0/0 | 4203 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0002t0004 | 0/0 | 4203 | 15 | 6 | 2 | 7 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0002t0011 | 0/0 | 4203 | 3 | 3 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0004t0004 | 0/0 | 4203 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0001c0007t0029 | 0/0 | 4202 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0002c0003t0002 | 0/0 | 4203 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0003c0005t0006 | 0/0 | 4203 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0004c0009t0002 | 0/0 | 4203 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0005c0008t0001 | 0/0 | 4202 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
a0006c0006t0001 | 0/0 | 4202 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | copy fasta | chr5 | 50391192 | 50446288 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0006g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0006g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0006g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0006g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0007g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0007g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0007g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0007g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0007g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0007g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0007g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0007g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0007g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0007g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0008g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0009g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0010g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0010g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0012g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0013g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0013g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0014g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0014g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0015g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0016g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0017g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0018g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0019g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0020g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0021g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0022g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0023g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0024g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0025g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0026g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0027g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0001t0028g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0002t0004g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0002t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0002t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0002t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0002t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0002t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0002t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0002t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0002t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0002t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0002t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0002t0011g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0002t0011g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0004t0004g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0001c0007t0029g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0002c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0002c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0003c0005t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0004c0009t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0005c0008t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
a0006c0006t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | GBR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00099 | hp2 | a0001 | c0001 | t0026 | g0136 | EUR | GBR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00280 | hp1 | a0001 | c0001 | t0007 | g0088 | EUR | FIN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | FIN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00323 | hp1 | a0001 | c0001 | t0006 | g0175 | EUR | FIN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | FIN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00544 | hp2 | a0001 | c0001 | t0014 | g0073 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00558 | hp1 | a0001 | c0001 | t0006 | g0154 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00597 | hp1 | a0001 | c0001 | t0013 | g0076 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0048 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00735 | hp1 | a0001 | c0001 | t0007 | g0168 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0245 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0159 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00741 | hp1 | a0001 | c0001 | t0007 | g0167 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01070 | hp1 | a0001 | c0001 | t0007 | g0018 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01071 | hp1 | a0001 | c0001 | t0007 | g0018 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0143 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01109 | hp2 | a0001 | c0002 | t0004 | g0031 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01167 | hp1 | a0001 | c0004 | t0004 | g0035 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0056 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01169 | hp1 | a0001 | c0004 | t0004 | g0035 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01192 | hp1 | a0001 | c0002 | t0004 | g0289 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01243 | hp2 | a0001 | c0001 | t0012 | g0052 | AMR | PUR | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01257 | hp1 | a0001 | c0001 | t0028 | g0144 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0042 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0061 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01358 | hp1 | a0001 | c0001 | t0023 | g0254 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01358 | hp2 | a0001 | c0001 | t0007 | g0125 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01361 | hp2 | a0001 | c0001 | t0006 | g0152 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0248 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0110 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | IBS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | IBS | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01884 | hp2 | a0001 | c0002 | t0011 | g0034 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01975 | hp1 | a0001 | c0001 | t0025 | g0142 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01978 | hp1 | a0001 | c0001 | t0024 | g0214 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02040 | hp2 | a0001 | c0001 | t0006 | g0021 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0252 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0089 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | KHV | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0059 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CDX | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CDX | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | CDX | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0186 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0101 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02280 | hp2 | a0001 | c0002 | t0004 | g0290 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02602 | hp1 | a0001 | c0001 | t0005 | g0246 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0249 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02647 | hp1 | a0001 | c0001 | t0009 | g0054 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02647 | hp2 | a0006 | c0006 | t0001 | g0038 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0046 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02723 | hp2 | a0001 | c0001 | t0020 | g0118 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0250 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0251 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02922 | hp2 | a0001 | c0001 | t0027 | g0064 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02976 | hp2 | a0001 | c0001 | t0010 | g0058 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03041 | hp2 | a0001 | c0001 | t0009 | g0051 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03098 | hp1 | a0001 | c0002 | t0004 | g0284 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03098 | hp2 | a0001 | c0002 | t0011 | g0287 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03130 | hp1 | a0001 | c0001 | t0021 | g0097 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03139 | hp1 | a0001 | c0001 | t0018 | g0119 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03139 | hp2 | a0001 | c0001 | t0008 | g0185 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0102 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0103 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0122 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0123 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03453 | hp2 | a0001 | c0002 | t0011 | g0034 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0141 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0065 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0279 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0045 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0149 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03710 | hp1 | a0001 | c0001 | t0007 | g0124 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03831 | hp1 | a0001 | c0001 | t0006 | g0157 | SAS | BEB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03831 | hp2 | a0001 | c0001 | t0007 | g0165 | SAS | BEB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03927 | hp1 | a0001 | c0001 | t0007 | g0127 | SAS | BEB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0011 | SAS | BEB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | BEB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0011 | SAS | STU | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG04115 | hp2 | a0001 | c0001 | t0007 | g0166 | SAS | STU | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | STU | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | STU | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18522 | hp1 | a0001 | c0001 | t0009 | g0071 | AFR | YRI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | YRI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18612 | hp1 | a0001 | c0001 | t0014 | g0079 | EAS | CHB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | YRI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | YRI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18942 | hp1 | a0004 | c0009 | t0002 | g0069 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18944 | hp1 | a0001 | c0002 | t0004 | g0293 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18945 | hp1 | a0001 | c0001 | t0006 | g0153 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18949 | hp1 | a0001 | c0001 | t0017 | g0200 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18961 | hp2 | a0001 | c0001 | t0013 | g0132 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18962 | hp1 | a0001 | c0001 | t0006 | g0116 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18962 | hp2 | a0001 | c0001 | t0019 | g0242 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18965 | hp2 | a0001 | c0001 | t0016 | g0074 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18975 | hp2 | a0002 | c0003 | t0002 | g0086 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18977 | hp1 | a0001 | c0002 | t0004 | g0032 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18991 | hp2 | a0001 | c0002 | t0004 | g0288 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19003 | hp2 | a0001 | c0007 | t0029 | g0283 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19006 | hp1 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19010 | hp1 | a0001 | c0002 | t0004 | g0033 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | LWK | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | LWK | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | LWK | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19043 | hp2 | a0001 | c0002 | t0004 | g0031 | AFR | LWK | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19054 | hp2 | a0001 | c0001 | t0006 | g0021 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19063 | hp1 | a0001 | c0002 | t0004 | g0032 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19064 | hp1 | a0001 | c0001 | t0015 | g0036 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19064 | hp2 | a0001 | c0001 | t0006 | g0156 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19065 | hp1 | a0002 | c0003 | t0002 | g0087 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19077 | hp1 | a0001 | c0001 | t0006 | g0158 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19081 | hp1 | a0001 | c0002 | t0004 | g0285 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19083 | hp2 | a0001 | c0002 | t0004 | g0033 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19086 | hp2 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19088 | hp1 | a0003 | c0005 | t0006 | g0037 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19240 | hp1 | a0001 | c0002 | t0004 | g0291 | AFR | YRI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | YRI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ASW | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ASW | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0092 | EUR | TSI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0247 | EUR | TSI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0135 | EUR | TSI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | TSI | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | GIH | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0155 | SAS | GIH | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02109 | hp1 | a0005 | c0008 | t0001 | g0260 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0100 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02486 | hp2 | a0001 | c0001 | t0012 | g0053 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | USA | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
HG06807 | hp2 | a0001 | c0001 | t0010 | g0057 | AFR | USA | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA20300 | hp1 | a0001 | c0001 | t0022 | g0237 | AFR | USA | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA20300 | hp2 | a0001 | c0002 | t0004 | g0286 | AFR | USA | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA21309 | hp1 | a0001 | c0002 | t0004 | g0292 | AFR | LWK | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0137 | REF | REF | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0198 | REF | REF | EMB_chr5_50391192_50446288 | EMB | chr5 | 50391192 | 50446288 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:50396192
|
T | C | 1 | a0001 | 1 | HG03130.hp1 | splice_region_variant | LOW | c.*3081A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | chr5 | 50396192 | ||||||
chr5:50403232
|
C | T | 1 | a0004 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.823G>A | p.Val275Met | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/9 | 960/4202 | 823/984 | 275/327 | chr5 | 50403232 | ||
chr5:50403375
|
A | G | 1 | a0005 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.680T>C | p.Leu227Pro | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/9 | 817/4202 | 680/984 | 227/327 | chr5 | 50403375 | ||
chr5:50410965
|
C | A | 1 | a0005 | 1 | HG02109.hp1 | missense_variant&splice_region_variant | MODERATE | c.384G>T | p.Arg128Ser | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/9 | 521/4202 | 384/984 | 128/327 | chr5 | 50410965 | ||
chr5:50411302
|
G | C | 2 | a0002a0004 | 3 | NA18942.hp1 NA18975.hp2 NA19065.hp1 |
missense_variant | MODERATE | c.278C>G | p.Ser93Cys | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 3/9 | 415/4202 | 278/984 | 93/327 | chr5 | 50411302 | ||
chr5:50441079
|
C | T | 1 | a0006 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.73G>A | p.Ala25Thr | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/9 | 210/4202 | 73/984 | 25/327 | chr5 | 50441079 | ||
chr5:50441150
|
A | T | 1 | a0003 | 1 | NA19088.hp1 | start_lost | HIGH | c.2T>A | p.Met1? | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/9 | 139/4202 | 2/984 | 1/327 | chr5 | 50441150 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:50403200
|
T | C | 1 | a0001c0004 | 2 | HG01167.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.855A>G | p.Thr285Thr | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/9 | 992/4202 | 855/984 | 285/327 | chr5 | 50403200 | ||
chr5:50403449
|
A | G | 1 | a0001c0007 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.606T>C | p.Pro202Pro | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/9 | 743/4202 | 606/984 | 202/327 | chr5 | 50403449 | ||
chr5:50441053
|
G | A | 1 | a0001c0002 | 18 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(15): Show |
synonymous_variant | LOW | c.99C>T | p.Asp33Asp | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/9 | 236/4202 | 99/984 | 33/327 | chr5 | 50441053 | ||
chr5:50441092
|
G | C | 1 | a0001c0004 | 2 | HG01167.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.60C>G | p.Leu20Leu | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/9 | 197/4202 | 60/984 | 20/327 | chr5 | 50441092 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:50396201
|
A | G | 1 | a0001c0001t0021 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3072T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 3072 | chr5 | 50396201 | |||||
chr5:50396209
|
G | A | 1 | a0001c0001t0007 | 12 | HG00280.hp1 HG00735.hp1 HG00741.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3064C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 3064 | chr5 | 50396209 | |||||
chr5:50396483
|
G | C | 1 | a0001c0001t0022 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2790C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 2790 | chr5 | 50396483 | |||||
chr5:50396742
|
C | T | 1 | a0001c0001t0016 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2531G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 2531 | chr5 | 50396742 | |||||
chr5:50396761
|
G | C | 2 | a0001c0001t0009a0001c0001t0012 | 6 | HG01243.hp2 HG02055.hp2 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2512C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 2512 | chr5 | 50396761 | |||||
chr5:50396796
|
G | GC | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*2476_*2477insG | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 2476 | chr5 | 50396796 | |||||
chr5:50397168
|
T | C | 1 | a0001c0001t0010 | 3 | HG02145.hp1 HG02976.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2105A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 2105 | chr5 | 50397168 | |||||
chr5:50397254
|
C | T | 1 | a0001c0001t0020 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2019G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 2019 | chr5 | 50397254 | |||||
chr5:50397297
|
C | T | 1 | a0001c0001t0020 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1976G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1976 | chr5 | 50397297 | |||||
chr5:50397336
|
A | G | 1 | a0001c0001t0019 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1937T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1937 | chr5 | 50397336 | |||||
chr5:50397624
|
C | T | 24 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(21): Show | 207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*1649G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1649 | chr5 | 50397624 | |||||
chr5:50397682
|
A | C | 1 | a0001c0001t0018 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1591T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1591 | chr5 | 50397682 | |||||
chr5:50397718
|
A | T | 1 | a0001c0007t0029 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1555T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1555 | chr5 | 50397718 | |||||
chr5:50397721
|
G | C | 1 | a0001c0001t0027 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1552C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1552 | chr5 | 50397721 | |||||
chr5:50397780
|
C | T | 1 | a0001c0002t0011 | 3 | HG01884.hp2 HG03098.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1493G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1493 | chr5 | 50397780 | |||||
chr5:50397934
|
T | C | 1 | a0001c0001t0008 | 5 | HG02055.hp1 HG02257.hp2 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1339A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1339 | chr5 | 50397934 | |||||
chr5:50397956
|
T | G | 1 | a0001c0001t0023 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1317A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1317 | chr5 | 50397956 | |||||
chr5:50398251
|
T | C | 1 | a0001c0001t0024 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1022A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 1022 | chr5 | 50398251 | |||||
chr5:50398309
|
G | A | 1 | a0001c0001t0013 | 2 | HG00597.hp1 NA18961.hp2 |
3_prime_UTR_variant | MODIFIER | c.*964C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 964 | chr5 | 50398309 | |||||
chr5:50398354
|
C | T | 1 | a0001c0001t0028 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*919G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 919 | chr5 | 50398354 | |||||
chr5:50398547
|
A | C | 1 | a0001c0001t0009 | 4 | HG02055.hp2 HG02647.hp1 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*726T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 726 | chr5 | 50398547 | |||||
chr5:50398564
|
A | G | 1 | a0001c0001t0017 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*709T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 709 | chr5 | 50398564 | |||||
chr5:50398749
|
T | G | 15 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(12): Show | 136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*524A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 524 | chr5 | 50398749 | |||||
chr5:50398799
|
A | G | 1 | a0001c0001t0026 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*474T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 474 | chr5 | 50398799 | |||||
chr5:50398878
|
T | A | 5 | a0001c0001t0004a0001c0001t0014a0001c0002t0004others(2): Show | 39 | HG00544.hp2 HG01109.hp2 HG01167.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*395A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 395 | chr5 | 50398878 | |||||
chr5:50398879
|
T | A | 23 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(20): Show | 206 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*394A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 394 | chr5 | 50398879 | |||||
chr5:50399127
|
G | A | 3 | a0001c0001t0006a0001c0007t0029a0003c0005t0006 | 16 | HG00323.hp1 HG00558.hp1 HG00738.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*146C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 146 | chr5 | 50399127 | |||||
chr5:50399214
|
C | T | 9 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(6): Show | 82 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*59G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 9/9 | 59 | chr5 | 50399214 | |||||
chr5:50441245
|
C | T | 1 | a0001c0001t0015 | 1 | NA19064.hp1 | 5_prime_UTR_variant | MODIFIER | c.-94G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/9 | 94 | chr5 | 50441245 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:50399316
|
T | C | 1 | a0001c0001t0005g0100 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.967-26A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 8/8 | chr5 | 50399316 | ||||||
chr5:50399492
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.967-202T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 8/8 | chr5 | 50399492 | ||||||
chr5:50399573
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.967-283T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 8/8 | chr5 | 50399573 | ||||||
chr5:50399602
|
G | A | 1 | a0001c0004t0004g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.966+257C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 8/8 | chr5 | 50399602 | ||||||
chr5:50399772
|
G | C | 1 | a0001c0001t0002g0111 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.966+87C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 8/8 | chr5 | 50399772 | ||||||
chr5:50399927
|
A | G | 2 | a0001c0001t0003g0009a0001c0001t0003g0161 | 3 | HG02486.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.912-14T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50399927 | ||||||
chr5:50399934
|
A | G | 1 | a0001c0001t0018g0119 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.912-21T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50399934 | ||||||
chr5:50399951
|
A | G | 1 | a0001c0001t0004g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.912-38T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50399951 | ||||||
chr5:50399974
|
A | C | 18 | a0001c0001t0004g0099a0001c0001t0010g0057a0001c0001t0010g0058others(15): Show | 22 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.912-61T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50399974 | ||||||
chr5:50400019
|
G | A | 4 | a0001c0001t0008g0023a0001c0001t0008g0185a0001c0001t0008g0186others(1): Show | 5 | HG02055.hp1 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.912-106C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400019 | ||||||
chr5:50400151
|
C | T | 1 | a0001c0001t0028g0144 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.912-238G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400151 | ||||||
chr5:50400380
|
G | A | 12 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0177others(9): Show | 14 | HG01358.hp1 HG02293.hp1 NA18747.hp2 others(11): Show |
intron_variant | MODIFIER | c.912-467C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400380 | ||||||
chr5:50400441
|
G | T | 175 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(172): Show | 207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.912-528C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400441 | ||||||
chr5:50400457
|
T | C | 8 | a0001c0001t0004g0010a0001c0001t0004g0039a0001c0001t0004g0040others(5): Show | 9 | HG01167.hp2 HG01261.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.912-544A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400457 | ||||||
chr5:50400691
|
T | C | 34 | a0001c0001t0004g0010a0001c0001t0004g0039a0001c0001t0004g0040others(31): Show | 40 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.912-778A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400691 | ||||||
chr5:50400745
|
T | C | 18 | a0001c0001t0004g0099a0001c0001t0010g0057a0001c0001t0010g0058others(15): Show | 22 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.912-832A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400745 | ||||||
chr5:50400765
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.912-852C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400765 | ||||||
chr5:50400811
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.912-898T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400811 | ||||||
chr5:50400905
|
C | T | 1 | a0001c0001t0004g0050 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.912-992G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400905 | ||||||
chr5:50400974
|
G | A | 8 | a0001c0001t0005g0011a0001c0001t0005g0045a0001c0001t0005g0046others(5): Show | 9 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.912-1061C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50400974 | ||||||
chr5:50401062
|
G | A | 1 | a0001c0001t0002g0077 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.912-1149C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401062 | ||||||
chr5:50401098
|
A | G | 148 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(145): Show | 176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.912-1185T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401098 | ||||||
chr5:50401306
|
C | T | 175 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(172): Show | 207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.911+980G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401306 | ||||||
chr5:50401402
|
T | A | 5 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0209others(2): Show | 5 | HG03490.hp2 HG03704.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.911+884A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401402 | ||||||
chr5:50401415
|
C | T | 1 | a0001c0001t0002g0111 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.911+871G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401415 | ||||||
chr5:50401488
|
G | A | 148 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(145): Show | 176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.911+798C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401488 | ||||||
chr5:50401495
|
T | A | 1 | a0001c0001t0003g0169 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.911+791A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401495 | ||||||
chr5:50401581
|
C | T | 2 | a0001c0001t0004g0039a0001c0001t0004g0043 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.911+705G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401581 | ||||||
chr5:50401594
|
G | A | 1 | a0001c0001t0004g0056 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.911+692C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401594 | ||||||
chr5:50401964
|
C | T | 1 | a0001c0001t0009g0051 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.911+322G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50401964 | ||||||
chr5:50402029
|
C | T | 114 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(111): Show | 136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.911+257G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50402029 | ||||||
chr5:50402124
|
C | T | 1 | a0001c0001t0005g0279 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.911+162G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50402124 | ||||||
chr5:50402173
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.911+113A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 7/8 | chr5 | 50402173 | ||||||
chr5:50402346
|
G | A | 176 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(173): Show | 208 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.878-27C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402346 | ||||||
chr5:50402392
|
C | A | 1 | a0001c0001t0005g0045 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.878-73G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402392 | ||||||
chr5:50402754
|
A | G | 1 | a0001c0007t0029g0283 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.877+424T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402754 | ||||||
chr5:50402777
|
G | C | 9 | a0001c0001t0005g0029a0001c0001t0005g0248a0001c0001t0005g0249others(6): Show | 11 | HG01433.hp2 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.877+401C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402777 | ||||||
chr5:50402789
|
CT | C | 8 | a0001c0001t0005g0016a0001c0001t0005g0065a0001c0001t0005g0100others(5): Show | 9 | HG02109.hp2 HG02280.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.877+388delA | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402789 | ||||||
chr5:50402876
|
C | CA | 14 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0262others(11): Show | 14 | HG00597.hp1 HG00738.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.877+301dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402876 | ||||||
chr5:50402876
|
C | CAA | 8 | a0001c0001t0002g0012a0001c0001t0002g0112a0001c0001t0004g0010others(5): Show | 10 | HG01261.hp1 HG01891.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.877+300_877+301dup others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402876 | ||||||
chr5:50402876
|
CA | C | 20 | a0001c0001t0001g0215a0001c0001t0001g0222a0001c0001t0001g0256others(17): Show | 20 | HG01167.hp2 HG01891.hp2 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.877+301delT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402876 | ||||||
chr5:50402876
|
CAA | C | 26 | a0001c0001t0005g0011a0001c0001t0005g0016a0001c0001t0005g0029others(23): Show | 30 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.877+300_877+301del others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50402876 | ||||||
chr5:50403151
|
AC | A | 3 | a0001c0001t0005g0248a0001c0002t0011g0034a0001c0002t0011g0287 | 4 | HG01433.hp2 HG01884.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.877+26delG | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50403151 | ||||||
chr5:50403152
|
C | A | 171 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(168): Show | 202 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.877+26G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50403152 | ||||||
chr5:50403159
|
C | A | 1 | a0001c0001t0002g0078 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.877+19G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 6/8 | chr5 | 50403159 | ||||||
chr5:50403892
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.601-438G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50403892 | ||||||
chr5:50403973
|
G | A | 1 | a0001c0004t0004g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.601-519C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50403973 | ||||||
chr5:50403997
|
G | C | 4 | a0001c0001t0004g0099a0001c0002t0004g0031a0001c0002t0004g0284others(1): Show | 5 | HG01109.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-543C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50403997 | ||||||
chr5:50404060
|
G | C | 114 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(111): Show | 136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.601-606C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404060 | ||||||
chr5:50404281
|
G | A | 1 | a0001c0001t0021g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.601-827C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404281 | ||||||
chr5:50404320
|
A | T | 1 | a0001c0001t0003g0161 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.601-866T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404320 | ||||||
chr5:50404569
|
C | T | 1 | a0001c0001t0007g0167 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.601-1115G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404569 | ||||||
chr5:50404627
|
T | C | 26 | a0001c0001t0005g0011a0001c0001t0005g0016a0001c0001t0005g0029others(23): Show | 30 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.600+1098A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404627 | ||||||
chr5:50404735
|
G | C | 1 | a0001c0001t0001g0201 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.600+990C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404735 | ||||||
chr5:50404795
|
A | G | 1 | a0001c0001t0004g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.600+930T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404795 | ||||||
chr5:50404872
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.600+853A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404872 | ||||||
chr5:50404968
|
T | C | 1 | a0001c0001t0003g0161 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.600+757A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404968 | ||||||
chr5:50404979
|
C | T | 1 | a0001c0001t0003g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.600+746G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50404979 | ||||||
chr5:50405386
|
T | TA | 3 | a0001c0001t0003g0133a0001c0001t0003g0134a0001c0001t0003g0146 | 3 | NA18961.hp1 NA18980.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.600+338dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50405386 | ||||||
chr5:50405486
|
A | T | 1 | a0001c0001t0002g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.600+239T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50405486 | ||||||
chr5:50405685
|
CTGT | C | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.600+37_600+39delAC others(1): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 5/8 | chr5 | 50405685 | ||||||
chr5:50405921
|
A | G | 176 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(173): Show | 208 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.473-69T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50405921 | ||||||
chr5:50406005
|
G | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0117others(5): Show | 10 | HG01192.hp2 HG01884.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.473-153C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50406005 | ||||||
chr5:50406142
|
G | C | 7 | a0001c0001t0004g0010a0001c0001t0004g0039a0001c0001t0004g0040others(4): Show | 8 | HG01261.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.473-290C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50406142 | ||||||
chr5:50406226
|
A | C | 1 | a0001c0001t0007g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.473-374T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50406226 | ||||||
chr5:50406236
|
A | G | 1 | a0001c0001t0003g0145 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.473-384T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50406236 | ||||||
chr5:50406413
|
A | T | 13 | a0001c0001t0004g0010a0001c0001t0004g0039a0001c0001t0004g0040others(10): Show | 15 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.473-561T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50406413 | ||||||
chr5:50406645
|
T | C | 1 | a0001c0001t0006g0022 | 2 | NA19006.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.473-793A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50406645 | ||||||
chr5:50406766
|
C | T | 116 | a0001c0001t0001g0025a0001c0001t0001g0201a0001c0001t0002g0001others(113): Show | 139 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.473-914G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50406766 | ||||||
chr5:50407046
|
ACT | A | 5 | a0001c0001t0004g0049a0001c0001t0004g0056a0001c0001t0004g0094others(2): Show | 5 | HG01167.hp2 HG02615.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.473-1196_473-1195d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407046 | ||||||
chr5:50407076
|
C | T | 1 | a0001c0001t0004g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.473-1224G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407076 | ||||||
chr5:50407325
|
G | A | 1 | a0001c0002t0004g0286 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.473-1473C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407325 | ||||||
chr5:50407336
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.473-1484T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407336 | ||||||
chr5:50407349
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.473-1497G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407349 | ||||||
chr5:50407354
|
C | CGCT | 13 | a0001c0001t0002g0012a0001c0001t0002g0062a0001c0001t0002g0066others(10): Show | 14 | HG01243.hp2 HG02055.hp2 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.473-1505_473-1503d others(5): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407354 | ||||||
chr5:50407632
|
C | A | 1 | a0001c0004t0004g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.473-1780G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407632 | ||||||
chr5:50407774
|
G | C | 154 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(151): Show | 183 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.473-1922C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407774 | ||||||
chr5:50407795
|
C | G | 188 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0117others(185): Show | 222 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.473-1943G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50407795 | ||||||
chr5:50408133
|
T | C | 1 | a0001c0001t0002g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.473-2281A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50408133 | ||||||
chr5:50408249
|
TA | T | 114 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(111): Show | 136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.473-2398delT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50408249 | ||||||
chr5:50408254
|
C | T | 175 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(172): Show | 207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.473-2402G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50408254 | ||||||
chr5:50408347
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.473-2495G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50408347 | ||||||
chr5:50408461
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.472+2416C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50408461 | ||||||
chr5:50408490
|
C | G | 1 | a0001c0001t0004g0160 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.472+2387G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50408490 | ||||||
chr5:50409276
|
C | T | 3 | a0001c0002t0004g0289a0001c0002t0004g0290a0001c0002t0004g0291 | 3 | HG01192.hp1 HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.472+1601G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50409276 | ||||||
chr5:50409378
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.472+1499C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50409378 | ||||||
chr5:50409567
|
G | A | 1 | a0001c0001t0007g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.472+1310C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50409567 | ||||||
chr5:50409661
|
G | T | 1 | a0001c0001t0025g0142 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.472+1216C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50409661 | ||||||
chr5:50409743
|
T | C | 50 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(47): Show | 65 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.472+1134A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50409743 | ||||||
chr5:50409913
|
T | C | 3 | a0001c0001t0001g0253a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG02056.hp1 NA19055.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.472+964A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50409913 | ||||||
chr5:50409921
|
A | G | 1 | a0002c0003t0002g0086 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.472+956T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50409921 | ||||||
chr5:50410001
|
A | G | 1 | a0001c0001t0004g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.472+876T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410001 | ||||||
chr5:50410080
|
G | A | 1 | a0001c0001t0004g0050 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.472+797C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410080 | ||||||
chr5:50410136
|
A | G | 175 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(172): Show | 207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.472+741T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410136 | ||||||
chr5:50410151
|
C | T | 2 | a0001c0001t0001g0211a0002c0003t0002g0086 | 2 | NA18975.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.472+726G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410151 | ||||||
chr5:50410155
|
G | A | 1 | a0001c0001t0006g0116 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.472+722C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410155 | ||||||
chr5:50410449
|
A | G | 3 | a0001c0001t0010g0057a0001c0001t0010g0058a0001c0001t0010g0059 | 3 | HG02145.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.472+428T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410449 | ||||||
chr5:50410493
|
C | G | 5 | a0001c0001t0004g0099a0001c0001t0005g0016a0001c0001t0005g0100others(2): Show | 6 | HG02109.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.472+384G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410493 | ||||||
chr5:50410558
|
G | T | 1 | a0001c0001t0021g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.472+319C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410558 | ||||||
chr5:50410643
|
G | T | 1 | a0001c0001t0005g0047 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.472+234C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410643 | ||||||
chr5:50410711
|
A | G | 1 | a0001c0001t0003g0171 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.472+166T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410711 | ||||||
chr5:50410819
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0163a0001c0001t0001g0264others(1): Show | 6 | HG01192.hp2 HG01884.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.472+58C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410819 | ||||||
chr5:50410833
|
T | C | 7 | a0001c0001t0004g0099a0001c0001t0005g0016a0001c0001t0005g0100others(4): Show | 8 | HG02109.hp2 HG02280.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.472+44A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410833 | ||||||
chr5:50410855
|
T | C | 17 | a0001c0001t0010g0057a0001c0001t0010g0058a0001c0001t0010g0059others(14): Show | 21 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.472+22A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 4/8 | chr5 | 50410855 | ||||||
chr5:50411662
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.197-279C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50411662 | ||||||
chr5:50411667
|
TACCCTAT others(3): Show |
T | 146 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(143): Show | 173 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.197-294_197-285del others(10): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50411667 | ||||||
chr5:50411794
|
T | G | 8 | a0001c0001t0005g0011a0001c0001t0005g0045a0001c0001t0005g0046others(5): Show | 9 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.197-411A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50411794 | ||||||
chr5:50411808
|
G | A | 2 | a0001c0001t0005g0029a0001c0001t0005g0248 | 3 | HG01433.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.197-425C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50411808 | ||||||
chr5:50412032
|
A | G | 1 | a0001c0001t0005g0065 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.197-649T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412032 | ||||||
chr5:50412047
|
T | G | 2 | a0001c0001t0003g0170a0001c0001t0003g0171 | 2 | HG02129.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.197-664A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412047 | ||||||
chr5:50412189
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0222 | 2 | HG03490.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.197-806T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412189 | ||||||
chr5:50412240
|
C | CCA | 29 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0117others(26): Show | 34 | HG01192.hp2 HG01433.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.197-859_197-858dup others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412240 | ||||||
chr5:50412253
|
C | CACACAG | 6 | a0001c0001t0005g0011a0001c0001t0005g0045a0001c0001t0005g0046others(3): Show | 7 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-871_197-870ins others(6): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412253 | ||||||
chr5:50412255
|
C | CACAG | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0005g0065 | 3 | HG02615.hp2 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.197-873_197-872ins others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412255 | ||||||
chr5:50412257
|
G | C | 11 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0005g0011others(8): Show | 12 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-874C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412257 | ||||||
chr5:50412257
|
G | GAC | 3 | a0001c0001t0001g0025a0001c0001t0001g0201a0001c0001t0001g0226 | 4 | HG01952.hp1 HG03017.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-876_197-875dup others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412257 | ||||||
chr5:50412257
|
GAC | G | 146 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(143): Show | 174 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.197-876_197-875del others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412257 | ||||||
chr5:50412258
|
A | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0223 | 2 | HG00140.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.197-875T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412258 | ||||||
chr5:50412304
|
C | T | 1 | a0001c0001t0021g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.197-921G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412304 | ||||||
chr5:50412353
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(62): Show | 82 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.197-970T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412353 | ||||||
chr5:50412396
|
A | G | 27 | a0001c0001t0004g0099a0001c0001t0005g0011a0001c0001t0005g0016others(24): Show | 31 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.197-1013T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412396 | ||||||
chr5:50412514
|
C | A | 1 | a0001c0001t0005g0102 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.197-1131G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412514 | ||||||
chr5:50412577
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.197-1194G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412577 | ||||||
chr5:50412624
|
C | T | 33 | a0001c0001t0004g0010a0001c0001t0004g0039a0001c0001t0004g0040others(30): Show | 39 | HG01109.hp2 HG01167.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.197-1241G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412624 | ||||||
chr5:50412662
|
AC | A | 114 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(111): Show | 136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.197-1280delG | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412662 | ||||||
chr5:50412696
|
T | C | 4 | a0001c0001t0009g0051a0001c0001t0009g0054a0001c0001t0009g0071others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-1313A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412696 | ||||||
chr5:50412701
|
C | T | 3 | a0001c0002t0004g0289a0001c0002t0004g0290a0001c0002t0004g0291 | 3 | HG01192.hp1 HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.197-1318G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412701 | ||||||
chr5:50412730
|
G | A | 1 | a0001c0001t0004g0160 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.197-1347C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412730 | ||||||
chr5:50412883
|
C | CT | 30 | a0001c0001t0001g0176a0001c0001t0001g0258a0001c0001t0002g0084others(27): Show | 34 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.197-1501dupA | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412883 | ||||||
chr5:50412917
|
T | C | 1 | a0001c0001t0001g0217 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.197-1534A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412917 | ||||||
chr5:50412918
|
G | C | 1 | a0001c0001t0001g0217 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.197-1535C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412918 | ||||||
chr5:50412919
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.197-1536C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412919 | ||||||
chr5:50412939
|
TAA | T | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.197-1558_197-1557d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50412939 | ||||||
chr5:50413049
|
C | T | 1 | a0001c0001t0004g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.197-1666G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413049 | ||||||
chr5:50413061
|
C | G | 6 | a0001c0001t0009g0051a0001c0001t0009g0054a0001c0001t0009g0071others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-1678G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413061 | ||||||
chr5:50413207
|
A | T | 1 | a0001c0001t0004g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.197-1824T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413207 | ||||||
chr5:50413215
|
G | A | 8 | a0001c0001t0005g0011a0001c0001t0005g0045a0001c0001t0005g0046others(5): Show | 9 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.197-1832C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413215 | ||||||
chr5:50413234
|
T | C | 114 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(111): Show | 136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.197-1851A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413234 | ||||||
chr5:50413269
|
T | C | 6 | a0001c0001t0004g0010a0001c0001t0004g0039a0001c0001t0004g0040others(3): Show | 7 | HG01261.hp1 HG01891.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-1886A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413269 | ||||||
chr5:50413461
|
T | G | 1 | a0001c0001t0001g0205 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.197-2078A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413461 | ||||||
chr5:50413584
|
C | CT | 7 | a0001c0001t0002g0092a0001c0001t0003g0009a0001c0001t0004g0061others(4): Show | 8 | HG00597.hp1 HG01346.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-2202dupA | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413584 | ||||||
chr5:50413616
|
C | A | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.197-2233G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413616 | ||||||
chr5:50413721
|
G | A | 114 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(111): Show | 136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.197-2338C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413721 | ||||||
chr5:50413880
|
C | T | 291 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(288): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.197-2497G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413880 | ||||||
chr5:50413914
|
G | A | 3 | a0001c0001t0006g0153a0001c0001t0006g0158a0003c0005t0006g0037 | 3 | NA18945.hp1 NA19077.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.197-2531C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413914 | ||||||
chr5:50413918
|
G | A | 1 | a0001c0001t0014g0079 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.197-2535C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413918 | ||||||
chr5:50413940
|
C | A | 114 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(111): Show | 136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.197-2557G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50413940 | ||||||
chr5:50414147
|
C | T | 1 | a0001c0001t0021g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.197-2764G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414147 | ||||||
chr5:50414387
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0202a0001c0001t0001g0204 | 4 | NA18747.hp2 NA18955.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-3004G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414387 | ||||||
chr5:50414421
|
C | T | 187 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0117others(184): Show | 221 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.197-3038G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414421 | ||||||
chr5:50414451
|
G | A | 1 | a0001c0001t0002g0111 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.197-3068C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414451 | ||||||
chr5:50414491
|
C | T | 6 | a0001c0002t0004g0032a0001c0002t0004g0033a0001c0002t0004g0285others(3): Show | 8 | NA18944.hp1 NA18977.hp1 NA18991.hp2 others(5): Show |
intron_variant | MODIFIER | c.197-3108G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414491 | ||||||
chr5:50414528
|
C | CA | 61 | a0001c0001t0001g0027a0001c0001t0001g0120a0001c0001t0001g0121others(58): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.197-3146dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414528 | ||||||
chr5:50414528
|
C | CAA | 5 | a0001c0001t0001g0098a0001c0001t0001g0216a0001c0001t0002g0015others(2): Show | 6 | HG01891.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-3147_197-3146d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414528 | ||||||
chr5:50414528
|
CA | C | 24 | a0001c0001t0001g0178a0001c0001t0001g0211a0001c0001t0001g0239others(21): Show | 25 | HG00438.hp1 HG00673.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.197-3146delT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414528 | ||||||
chr5:50414528
|
CAA | C | 78 | a0001c0001t0002g0075a0001c0001t0002g0080a0001c0001t0002g0105others(75): Show | 90 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.197-3147_197-3146d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414528 | ||||||
chr5:50414787
|
C | T | 5 | a0001c0001t0004g0099a0001c0001t0005g0016a0001c0001t0005g0100others(2): Show | 6 | HG02109.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-3404G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414787 | ||||||
chr5:50414803
|
C | G | 3 | a0001c0001t0006g0153a0001c0001t0006g0158a0003c0005t0006g0037 | 3 | NA18945.hp1 NA19077.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.197-3420G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414803 | ||||||
chr5:50414876
|
T | G | 48 | a0001c0001t0002g0105a0001c0001t0003g0019a0001c0001t0003g0020others(45): Show | 52 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.197-3493A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414876 | ||||||
chr5:50414955
|
T | A | 1 | a0001c0001t0003g0150 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.197-3572A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50414955 | ||||||
chr5:50415035
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.197-3652C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415035 | ||||||
chr5:50415056
|
C | T | 4 | a0001c0001t0001g0206a0001c0001t0001g0220a0001c0001t0001g0221others(1): Show | 4 | HG02602.hp2 HG02698.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-3673G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415056 | ||||||
chr5:50415061
|
A | G | 175 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(172): Show | 207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.197-3678T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415061 | ||||||
chr5:50415151
|
A | C | 1 | a0001c0001t0001g0194 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.197-3768T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415151 | ||||||
chr5:50415165
|
A | G | 2 | a0001c0002t0004g0289a0001c0002t0004g0290 | 2 | HG01192.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.197-3782T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415165 | ||||||
chr5:50415180
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.197-3797C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415180 | ||||||
chr5:50415305
|
T | C | 1 | a0001c0001t0016g0074 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.197-3922A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415305 | ||||||
chr5:50415319
|
A | C | 1 | a0001c0001t0016g0074 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.197-3936T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415319 | ||||||
chr5:50415453
|
C | T | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.197-4070G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415453 | ||||||
chr5:50415726
|
T | A | 1 | a0001c0001t0001g0182 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.197-4343A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415726 | ||||||
chr5:50415727
|
G | T | 1 | a0001c0001t0001g0182 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.197-4344C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415727 | ||||||
chr5:50415806
|
T | C | 1 | a0001c0001t0028g0144 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.197-4423A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50415806 | ||||||
chr5:50416184
|
C | G | 1 | a0001c0007t0029g0283 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.197-4801G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50416184 | ||||||
chr5:50416427
|
T | G | 1 | a0001c0002t0004g0033 | 2 | NA19010.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.197-5044A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50416427 | ||||||
chr5:50416652
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.197-5269A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50416652 | ||||||
chr5:50416720
|
G | C | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.197-5337C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50416720 | ||||||
chr5:50416792
|
G | A | 1 | a0001c0001t0003g0009 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.197-5409C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50416792 | ||||||
chr5:50416820
|
G | T | 1 | a0001c0002t0004g0285 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.197-5437C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50416820 | ||||||
chr5:50417003
|
G | A | 1 | a0001c0001t0005g0065 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.197-5620C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417003 | ||||||
chr5:50417164
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.197-5781A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417164 | ||||||
chr5:50417335
|
T | C | 1 | a0001c0001t0002g0084 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.197-5952A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417335 | ||||||
chr5:50417438
|
T | C | 1 | a0001c0001t0004g0042 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.197-6055A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417438 | ||||||
chr5:50417517
|
CAATGTGA others(27): Show |
C | 1 | a0001c0001t0002g0093 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.197-6168_197-6135d others(36): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417517 | ||||||
chr5:50417695
|
C | G | 3 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0113 | 3 | HG02615.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.197-6312G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417695 | ||||||
chr5:50417763
|
T | C | 28 | a0001c0001t0001g0120a0001c0001t0004g0010a0001c0001t0004g0039others(25): Show | 33 | HG01109.hp2 HG01192.hp1 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.197-6380A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417763 | ||||||
chr5:50417883
|
A | G | 2 | a0001c0001t0005g0029a0001c0001t0005g0248 | 3 | HG01433.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.197-6500T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417883 | ||||||
chr5:50417991
|
A | G | 2 | a0001c0001t0003g0009a0001c0001t0003g0161 | 3 | HG02486.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.197-6608T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50417991 | ||||||
chr5:50418289
|
C | G | 1 | a0001c0001t0027g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.197-6906G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418289 | ||||||
chr5:50418349
|
C | T | 1 | a0001c0004t0004g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.197-6966G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418349 | ||||||
chr5:50418388
|
C | T | 1 | a0001c0004t0004g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.197-7005G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418388 | ||||||
chr5:50418557
|
T | C | 27 | a0001c0001t0004g0099a0001c0001t0005g0011a0001c0001t0005g0016others(24): Show | 31 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.197-7174A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418557 | ||||||
chr5:50418596
|
T | C | 1 | a0001c0001t0003g0150 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.197-7213A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418596 | ||||||
chr5:50418601
|
C | T | 2 | a0001c0001t0026g0136a0001c0007t0029g0283 | 2 | HG00099.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.197-7218G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418601 | ||||||
chr5:50418636
|
G | A | 4 | a0001c0001t0009g0051a0001c0001t0009g0054a0001c0001t0009g0071others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-7253C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418636 | ||||||
chr5:50418929
|
T | C | 1 | a0001c0001t0002g0012 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.197-7546A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418929 | ||||||
chr5:50418992
|
T | C | 1 | a0001c0001t0005g0065 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.197-7609A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50418992 | ||||||
chr5:50419055
|
C | T | 1 | a0001c0007t0029g0283 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.197-7672G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419055 | ||||||
chr5:50419059
|
T | C | 1 | a0001c0001t0003g0135 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.197-7676A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419059 | ||||||
chr5:50419091
|
A | G | 4 | a0001c0001t0004g0049a0001c0001t0004g0094a0001c0001t0004g0095others(1): Show | 4 | HG02615.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-7708T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419091 | ||||||
chr5:50419135
|
G | C | 1 | a0006c0006t0001g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.197-7752C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419135 | ||||||
chr5:50419146
|
C | A | 1 | a0001c0001t0004g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.197-7763G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419146 | ||||||
chr5:50419343
|
C | T | 1 | a0001c0001t0013g0132 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.197-7960G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419343 | ||||||
chr5:50419422
|
C | T | 1 | a0001c0001t0003g0145 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.197-8039G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419422 | ||||||
chr5:50419532
|
TACATACA others(5): Show |
T | 7 | a0001c0001t0001g0026a0001c0001t0001g0208a0001c0001t0001g0241others(4): Show | 8 | HG00673.hp2 HG02056.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.197-8161_197-8150d others(14): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419532 | ||||||
chr5:50419536
|
T | TACAC | 3 | a0001c0001t0002g0015a0001c0001t0002g0107a0001c0001t0003g0161 | 4 | HG02258.hp2 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-8157_197-8154d others(6): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | ||||||
chr5:50419536
|
T | TACACAC | 4 | a0001c0001t0002g0013a0001c0001t0002g0085a0001c0001t0002g0090others(1): Show | 5 | HG00609.hp2 HG00639.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-8159_197-8154d others(8): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | ||||||
chr5:50419536
|
T | TACACACA others(1): Show |
41 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(38): Show | 54 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.197-8161_197-8154d others(10): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | ||||||
chr5:50419536
|
T | TACACACA others(3): Show |
18 | a0001c0001t0002g0017a0001c0001t0002g0055a0001c0001t0002g0062others(15): Show | 19 | HG00642.hp1 HG01496.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.197-8163_197-8154d others(12): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | ||||||
chr5:50419536
|
T | TACACACA others(5): Show |
9 | a0001c0001t0002g0014a0001c0001t0002g0082a0001c0001t0003g0135others(6): Show | 10 | HG00544.hp1 HG01361.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.197-8154_197-8153i others(14): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | ||||||
chr5:50419536
|
T | TACACACA others(7): Show |
11 | a0001c0001t0002g0091a0001c0001t0002g0105a0001c0001t0002g0111others(8): Show | 11 | HG00438.hp1 HG01081.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-8154_197-8153i others(16): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | ||||||
chr5:50419536
|
T | TACACACA others(9): Show |
25 | a0001c0001t0003g0019a0001c0001t0003g0044a0001c0001t0003g0115others(22): Show | 28 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.197-8154_197-8153i others(18): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | ||||||
chr5:50419536
|
T | TACACACA others(11): Show |
4 | a0001c0001t0003g0020a0001c0001t0003g0133a0001c0001t0003g0174others(1): Show | 5 | HG02040.hp1 HG02080.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-8154_197-8153i others(20): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | ||||||
chr5:50419536
|
T | TACACACA others(13): Show |
2 | a0001c0001t0003g0131a0001c0001t0003g0148 | 2 | HG02056.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.197-8154_197-8153i others(22): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419536 | ||||||
chr5:50419548
|
T | C | 118 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(115): Show | 140 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.197-8165A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419548 | ||||||
chr5:50419548
|
T | TACACAC | 3 | a0001c0001t0005g0250a0001c0001t0008g0185a0001c0001t0008g0252 | 3 | HG02055.hp1 HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.197-8171_197-8166d others(8): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419548 | ||||||
chr5:50419548
|
T | TACACACA others(1): Show |
15 | a0001c0001t0004g0010a0001c0001t0004g0099a0001c0001t0005g0016others(12): Show | 19 | HG01192.hp1 HG01433.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.197-8173_197-8166d others(10): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419548 | ||||||
chr5:50419548
|
T | TACACACA others(3): Show |
34 | a0001c0001t0004g0039a0001c0001t0004g0040a0001c0001t0004g0041others(31): Show | 39 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.197-8175_197-8166d others(12): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419548 | ||||||
chr5:50419548
|
T | TACACACA others(5): Show |
3 | a0001c0001t0004g0050a0001c0001t0004g0129a0001c0004t0004g0035 | 4 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-8177_197-8166d others(14): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419548 | ||||||
chr5:50419570
|
C | CACACACA others(5): Show |
1 | a0001c0001t0004g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.197-8188_197-8187i others(14): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419570 | ||||||
chr5:50419629
|
T | C | 27 | a0001c0001t0004g0099a0001c0001t0005g0011a0001c0001t0005g0016others(24): Show | 31 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.197-8246A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419629 | ||||||
chr5:50419751
|
T | C | 1 | a0001c0001t0002g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.197-8368A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419751 | ||||||
chr5:50419810
|
A | C | 1 | a0001c0001t0004g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.196+8334T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419810 | ||||||
chr5:50419945
|
C | T | 2 | a0001c0002t0011g0034a0001c0002t0011g0287 | 3 | HG01884.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.196+8199G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419945 | ||||||
chr5:50419968
|
G | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0232 | 2 | HG01515.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.196+8176C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50419968 | ||||||
chr5:50420033
|
AG | A | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.196+8110delC | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420033 | ||||||
chr5:50420073
|
T | C | 1 | a0001c0001t0005g0279 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196+8071A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420073 | ||||||
chr5:50420076
|
T | C | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.196+8068A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420076 | ||||||
chr5:50420213
|
C | T | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.196+7931G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420213 | ||||||
chr5:50420249
|
A | T | 1 | a0001c0001t0004g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196+7895T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420249 | ||||||
chr5:50420360
|
T | C | 1 | a0001c0001t0004g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.196+7784A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420360 | ||||||
chr5:50420445
|
T | G | 1 | a0001c0001t0006g0156 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.196+7699A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420445 | ||||||
chr5:50420626
|
T | G | 3 | a0001c0002t0004g0289a0001c0002t0004g0290a0001c0002t0004g0291 | 3 | HG01192.hp1 HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.196+7518A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420626 | ||||||
chr5:50420667
|
C | T | 33 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0044others(30): Show | 35 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.196+7477G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420667 | ||||||
chr5:50420668
|
G | T | 1 | a0001c0001t0004g0160 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.196+7476C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420668 | ||||||
chr5:50420748
|
G | A | 1 | a0001c0001t0012g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.196+7396C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420748 | ||||||
chr5:50420798
|
T | G | 1 | a0001c0001t0004g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196+7346A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50420798 | ||||||
chr5:50421011
|
A | G | 2 | a0001c0001t0001g0239a0001c0001t0001g0280 | 2 | HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.196+7133T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421011 | ||||||
chr5:50421107
|
C | T | 1 | a0001c0001t0003g0161 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196+7037G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421107 | ||||||
chr5:50421237
|
T | C | 27 | a0001c0001t0004g0010a0001c0001t0004g0039a0001c0001t0004g0040others(24): Show | 32 | HG01109.hp2 HG01192.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.196+6907A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421237 | ||||||
chr5:50421288
|
G | GA | 9 | a0001c0001t0005g0029a0001c0001t0005g0248a0001c0001t0005g0249others(6): Show | 11 | HG01433.hp2 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+6855dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421288 | ||||||
chr5:50421315
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.196+6829G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421315 | ||||||
chr5:50421635
|
A | G | 175 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(172): Show | 207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.196+6509T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421635 | ||||||
chr5:50421640
|
C | T | 1 | a0001c0001t0004g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.196+6504G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421640 | ||||||
chr5:50421749
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.196+6395G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421749 | ||||||
chr5:50421910
|
G | A | 1 | a0001c0007t0029g0283 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.196+6234C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421910 | ||||||
chr5:50421919
|
T | C | 1 | a0001c0007t0029g0283 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.196+6225A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421919 | ||||||
chr5:50421945
|
A | G | 114 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(111): Show | 136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.196+6199T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421945 | ||||||
chr5:50421952
|
G | C | 1 | a0001c0007t0029g0283 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.196+6192C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50421952 | ||||||
chr5:50422047
|
A | T | 1 | a0001c0001t0006g0175 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.196+6097T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422047 | ||||||
chr5:50422203
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.196+5941T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422203 | ||||||
chr5:50422209
|
C | A | 1 | a0001c0001t0002g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.196+5935G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422209 | ||||||
chr5:50422243
|
T | C | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.196+5901A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422243 | ||||||
chr5:50422314
|
T | C | 175 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(172): Show | 207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.196+5830A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422314 | ||||||
chr5:50422343
|
A | G | 2 | a0001c0001t0003g0140a0001c0001t0003g0141 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.196+5801T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422343 | ||||||
chr5:50422655
|
G | T | 1 | a0001c0001t0004g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.196+5489C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422655 | ||||||
chr5:50422743
|
C | T | 1 | a0001c0001t0005g0016 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.196+5401G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422743 | ||||||
chr5:50422825
|
G | A | 5 | a0001c0001t0005g0029a0001c0001t0005g0248a0001c0001t0005g0249others(2): Show | 6 | HG01433.hp2 HG02622.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+5319C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422825 | ||||||
chr5:50422863
|
G | A | 1 | a0005c0008t0001g0260 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+5281C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422863 | ||||||
chr5:50422949
|
T | C | 1 | a0001c0001t0005g0047 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.196+5195A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50422949 | ||||||
chr5:50423100
|
T | C | 1 | a0001c0001t0009g0054 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.196+5044A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423100 | ||||||
chr5:50423101
|
TA | T | 10 | a0001c0001t0001g0177a0001c0001t0001g0193a0001c0001t0001g0203others(7): Show | 11 | HG01109.hp2 HG01891.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.196+5042delT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423101 | ||||||
chr5:50423200
|
A | G | 1 | a0001c0001t0004g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.196+4944T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423200 | ||||||
chr5:50423297
|
C | T | 1 | a0001c0001t0004g0160 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.196+4847G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423297 | ||||||
chr5:50423329
|
G | C | 1 | a0001c0007t0029g0283 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.196+4815C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423329 | ||||||
chr5:50423331
|
G | C | 1 | a0001c0001t0004g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.196+4813C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423331 | ||||||
chr5:50423442
|
A | G | 1 | a0001c0001t0003g0133 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.196+4702T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423442 | ||||||
chr5:50423630
|
G | A | 1 | a0001c0001t0004g0160 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.196+4514C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423630 | ||||||
chr5:50423638
|
C | T | 1 | a0001c0001t0003g0139 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.196+4506G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423638 | ||||||
chr5:50423682
|
T | C | 2 | a0001c0001t0005g0250a0001c0001t0005g0251 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.196+4462A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423682 | ||||||
chr5:50423772
|
G | T | 48 | a0001c0001t0002g0105a0001c0001t0003g0019a0001c0001t0003g0020others(45): Show | 52 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.196+4372C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423772 | ||||||
chr5:50423775
|
G | A | 1 | a0001c0001t0002g0067 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.196+4369C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423775 | ||||||
chr5:50423788
|
C | T | 47 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0044others(44): Show | 51 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+4356G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423788 | ||||||
chr5:50423846
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0255a0001c0001t0001g0258others(1): Show | 7 | NA18942.hp2 NA19010.hp2 NA19057.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+4298T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50423846 | ||||||
chr5:50424357
|
G | C | 114 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(111): Show | 136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.196+3787C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50424357 | ||||||
chr5:50424527
|
C | T | 1 | a0001c0001t0006g0159 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.196+3617G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50424527 | ||||||
chr5:50424579
|
T | G | 1 | a0001c0001t0002g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.196+3565A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50424579 | ||||||
chr5:50425120
|
T | C | 1 | a0001c0001t0004g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.196+3024A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425120 | ||||||
chr5:50425262
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0162a0001c0001t0001g0176 | 3 | HG02559.hp1 HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.196+2882G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425262 | ||||||
chr5:50425303
|
C | T | 1 | a0001c0001t0004g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.196+2841G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425303 | ||||||
chr5:50425497
|
G | GA | 27 | a0001c0001t0004g0099a0001c0001t0005g0011a0001c0001t0005g0016others(24): Show | 31 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.196+2646dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425497 | ||||||
chr5:50425505
|
C | CA | 5 | a0001c0001t0001g0025a0001c0001t0001g0201a0001c0001t0001g0205others(2): Show | 6 | HG01952.hp1 HG03017.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+2638dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425505 | ||||||
chr5:50425512
|
A | T | 8 | a0001c0001t0005g0011a0001c0001t0005g0045a0001c0001t0005g0046others(5): Show | 9 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.196+2632T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425512 | ||||||
chr5:50425721
|
G | A | 7 | a0001c0001t0004g0010a0001c0001t0004g0039a0001c0001t0004g0040others(4): Show | 8 | HG01261.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.196+2423C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425721 | ||||||
chr5:50425735
|
T | TTGCTCTG others(15): Show |
188 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0117others(185): Show | 222 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.196+2408_196+2409i others(24): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425735 | ||||||
chr5:50425739
|
A | C | 9 | a0001c0001t0005g0029a0001c0001t0005g0248a0001c0001t0005g0249others(6): Show | 11 | HG01433.hp2 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+2405T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425739 | ||||||
chr5:50425752
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.196+2392G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425752 | ||||||
chr5:50425769
|
C | T | 47 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0044others(44): Show | 51 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.196+2375G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425769 | ||||||
chr5:50425894
|
G | A | 1 | a0004c0009t0002g0069 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.196+2250C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50425894 | ||||||
chr5:50426172
|
A | G | 1 | a0001c0004t0004g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.196+1972T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426172 | ||||||
chr5:50426240
|
T | G | 1 | a0001c0001t0003g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.196+1904A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426240 | ||||||
chr5:50426561
|
A | C | 1 | a0001c0001t0014g0073 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.196+1583T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426561 | ||||||
chr5:50426607
|
T | G | 1 | a0001c0004t0004g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.196+1537A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426607 | ||||||
chr5:50426794
|
A | G | 1 | a0001c0001t0002g0072 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.196+1350T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426794 | ||||||
chr5:50426898
|
G | GA | 10 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0117others(7): Show | 12 | HG01192.hp2 HG01884.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.196+1245dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426898 | ||||||
chr5:50426898
|
GA | G | 135 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(132): Show | 161 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.196+1245delT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426898 | ||||||
chr5:50426920
|
T | C | 1 | a0001c0001t0004g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196+1224A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426920 | ||||||
chr5:50426934
|
C | T | 1 | a0001c0001t0004g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196+1210G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50426934 | ||||||
chr5:50427045
|
T | C | 1 | a0001c0007t0029g0283 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.196+1099A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50427045 | ||||||
chr5:50427215
|
G | A | 1 | a0001c0001t0007g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.196+929C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50427215 | ||||||
chr5:50427234
|
C | T | 64 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(61): Show | 81 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.196+910G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50427234 | ||||||
chr5:50427489
|
C | CATT | 56 | a0001c0001t0002g0105a0001c0001t0003g0019a0001c0001t0003g0020others(53): Show | 61 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.196+652_196+654dup others(3): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50427489 | ||||||
chr5:50427489
|
CATT | C | 19 | a0001c0001t0004g0050a0001c0001t0004g0061a0001c0001t0010g0057others(16): Show | 23 | HG01109.hp2 HG01192.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.196+652_196+654del others(3): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50427489 | ||||||
chr5:50427700
|
G | A | 1 | a0001c0001t0002g0083 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.196+444C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 2/8 | chr5 | 50427700 | ||||||
chr5:50428398
|
T | C | 1 | a0001c0001t0005g0046 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.113-171A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50428398 | ||||||
chr5:50428437
|
C | T | 1 | a0001c0001t0003g0138 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.113-210G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50428437 | ||||||
chr5:50428615
|
G | A | 17 | a0001c0001t0010g0057a0001c0001t0010g0058a0001c0001t0010g0059others(14): Show | 21 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.113-388C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50428615 | ||||||
chr5:50428745
|
G | T | 6 | a0001c0001t0004g0010a0001c0001t0004g0039a0001c0001t0004g0040others(3): Show | 7 | HG01261.hp1 HG01891.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-518C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50428745 | ||||||
chr5:50428750
|
G | A | 2 | a0001c0001t0003g0009a0001c0001t0003g0161 | 3 | HG02486.hp1 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.113-523C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50428750 | ||||||
chr5:50428880
|
A | ATTTATT | 6 | a0001c0001t0004g0099a0001c0001t0005g0016a0001c0001t0005g0100others(3): Show | 7 | HG02109.hp2 HG02280.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-659_113-654dup others(6): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50428880 | ||||||
chr5:50428880
|
A | ATTTATTT others(5): Show |
1 | a0001c0001t0005g0102 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.113-665_113-654dup others(12): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50428880 | ||||||
chr5:50429075
|
T | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0210 | 2 | HG01261.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.113-848A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429075 | ||||||
chr5:50429487
|
A | C | 1 | a0001c0001t0021g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.113-1260T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429487 | ||||||
chr5:50429499
|
A | G | 9 | a0001c0001t0005g0011a0001c0001t0005g0045a0001c0001t0005g0046others(6): Show | 10 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-1272T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429499 | ||||||
chr5:50429522
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.113-1295C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429522 | ||||||
chr5:50429879
|
C | T | 1 | a0001c0001t0003g0169 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.113-1652G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429879 | ||||||
chr5:50429968
|
T | TTC | 21 | a0001c0001t0001g0007a0001c0001t0001g0162a0001c0001t0001g0163others(18): Show | 23 | HG00738.hp1 HG01192.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.113-1743_113-1742d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | ||||||
chr5:50429968
|
T | TTCTC | 12 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0120others(9): Show | 14 | HG00673.hp2 HG01243.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.113-1745_113-1742d others(6): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | ||||||
chr5:50429968
|
T | TTCTCTC | 6 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0208others(3): Show | 6 | HG01261.hp2 HG01433.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.113-1747_113-1742d others(8): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | ||||||
chr5:50429968
|
TTC | T | 18 | a0001c0001t0001g0098a0001c0001t0001g0184a0001c0001t0001g0191others(15): Show | 19 | HG00639.hp1 HG01358.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.113-1743_113-1742d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | ||||||
chr5:50429968
|
TTCTC | T | 28 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0229others(25): Show | 31 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.113-1745_113-1742d others(6): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | ||||||
chr5:50429968
|
TTCTCTC | T | 64 | a0001c0001t0001g0213a0001c0001t0001g0273a0001c0001t0002g0105others(61): Show | 73 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.113-1747_113-1742d others(8): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | ||||||
chr5:50429968
|
TTCTCTCT others(1): Show |
T | 3 | a0001c0001t0003g0009a0001c0001t0003g0161a0001c0001t0005g0251 | 4 | HG02486.hp1 HG02896.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-1749_113-1742d others(10): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | ||||||
chr5:50429968
|
TTCTCTCT others(3): Show |
T | 18 | a0001c0001t0001g0190a0001c0001t0001g0212a0001c0001t0002g0112others(15): Show | 19 | HG00099.hp2 HG01069.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.113-1751_113-1742d others(12): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | ||||||
chr5:50429968
|
TTCTCTCT others(5): Show |
T | 1 | a0001c0001t0002g0012 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.113-1753_113-1742d others(14): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | ||||||
chr5:50429968
|
TTCTCTCT others(7): Show |
T | 61 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(58): Show | 77 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.113-1755_113-1742d others(16): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | ||||||
chr5:50429968
|
TTCTCTCT others(11): Show |
T | 1 | a0001c0001t0002g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.113-1759_113-1742d others(20): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429968 | ||||||
chr5:50429970
|
C | T | 1 | a0001c0001t0005g0102 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.113-1743G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429970 | ||||||
chr5:50429972
|
C | T | 7 | a0001c0001t0004g0099a0001c0001t0005g0016a0001c0001t0005g0100others(4): Show | 8 | HG02109.hp2 HG02280.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-1745G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429972 | ||||||
chr5:50429974
|
C | T | 22 | a0001c0001t0004g0050a0001c0001t0004g0061a0001c0001t0004g0095others(19): Show | 25 | HG00642.hp2 HG01109.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.113-1747G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429974 | ||||||
chr5:50429976
|
C | T | 63 | a0001c0001t0002g0105a0001c0001t0003g0019a0001c0001t0003g0020others(60): Show | 72 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.113-1749G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429976 | ||||||
chr5:50429978
|
C | T | 10 | a0001c0001t0003g0009a0001c0001t0003g0161a0001c0001t0005g0011others(7): Show | 12 | HG00735.hp2 HG01074.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.113-1751G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429978 | ||||||
chr5:50429980
|
C | T | 14 | a0001c0001t0002g0112a0001c0001t0003g0122a0001c0001t0003g0130others(11): Show | 15 | HG00099.hp2 HG01069.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.113-1753G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429980 | ||||||
chr5:50429982
|
C | T | 1 | a0001c0001t0002g0012 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.113-1755G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429982 | ||||||
chr5:50429984
|
C | T | 61 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(58): Show | 77 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.113-1757G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429984 | ||||||
chr5:50429988
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.113-1761G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429988 | ||||||
chr5:50429997
|
T | A | 1 | a0001c0001t0004g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.113-1770A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429997 | ||||||
chr5:50429999
|
T | A | 18 | a0001c0001t0002g0112a0001c0001t0004g0129a0001c0001t0005g0102others(15): Show | 21 | HG01109.hp2 HG01192.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.113-1772A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50429999 | ||||||
chr5:50430001
|
T | A | 32 | a0001c0001t0002g0012a0001c0001t0002g0112a0001c0001t0003g0009others(29): Show | 39 | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.113-1774A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430001 | ||||||
chr5:50430003
|
T | A | 156 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(153): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.113-1776A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430003 | ||||||
chr5:50430005
|
T | A | 168 | a0001c0001t0001g0263a0001c0001t0002g0001a0001c0001t0002g0005others(165): Show | 199 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.113-1778A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430005 | ||||||
chr5:50430034
|
T | C | 1 | a0001c0001t0006g0116 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.113-1807A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430034 | ||||||
chr5:50430069
|
G | A | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.113-1842C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430069 | ||||||
chr5:50430168
|
C | T | 2 | a0001c0001t0002g0012a0001c0001t0002g0112 | 3 | HG02976.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.113-1941G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430168 | ||||||
chr5:50430232
|
T | C | 1 | a0001c0004t0004g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.113-2005A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430232 | ||||||
chr5:50430310
|
A | G | 7 | a0001c0001t0004g0010a0001c0001t0004g0039a0001c0001t0004g0040others(4): Show | 8 | HG01261.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-2083T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430310 | ||||||
chr5:50430406
|
C | A | 1 | a0001c0001t0001g0211 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.113-2179G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430406 | ||||||
chr5:50430521
|
T | C | 148 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0005others(145): Show | 176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.113-2294A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430521 | ||||||
chr5:50430589
|
TG | T | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.113-2363delC | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430589 | ||||||
chr5:50430593
|
T | C | 188 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0117others(185): Show | 222 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.113-2366A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430593 | ||||||
chr5:50430627
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0267 | 2 | HG01346.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.113-2400C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430627 | ||||||
chr5:50430668
|
T | G | 1 | a0001c0001t0005g0046 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.113-2441A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430668 | ||||||
chr5:50430739
|
T | C | 8 | a0001c0001t0005g0011a0001c0001t0005g0045a0001c0001t0005g0046others(5): Show | 9 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.113-2512A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50430739 | ||||||
chr5:50431146
|
T | C | 1 | a0001c0001t0004g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.113-2919A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50431146 | ||||||
chr5:50431463
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.113-3236A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50431463 | ||||||
chr5:50431475
|
C | T | 1 | a0001c0001t0002g0070 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.113-3248G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50431475 | ||||||
chr5:50431586
|
AAT | A | 8 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0215others(5): Show | 8 | HG01978.hp1 HG02132.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-3361_113-3360d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50431586 | ||||||
chr5:50431629
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.113-3402C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50431629 | ||||||
chr5:50431884
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.113-3657T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50431884 | ||||||
chr5:50432029
|
C | T | 1 | a0002c0003t0002g0086 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.113-3802G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432029 | ||||||
chr5:50432180
|
A | G | 1 | a0001c0001t0007g0018 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.113-3953T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432180 | ||||||
chr5:50432334
|
AT | A | 4 | a0001c0001t0008g0023a0001c0001t0008g0185a0001c0001t0008g0186others(1): Show | 5 | HG02055.hp1 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-4108delA | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432334 | ||||||
chr5:50432346
|
A | C | 1 | a0001c0001t0021g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.113-4119T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432346 | ||||||
chr5:50432369
|
C | A | 50 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(47): Show | 65 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.113-4142G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432369 | ||||||
chr5:50432562
|
T | TTAAAATA others(13): Show |
2 | a0001c0002t0011g0034a0001c0002t0011g0287 | 3 | HG01884.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.113-4355_113-4336d others(22): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432562 | ||||||
chr5:50432750
|
T | TA | 66 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0117others(63): Show | 75 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.113-4524dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432750 | ||||||
chr5:50432750
|
T | TAA | 6 | a0001c0001t0001g0120a0001c0001t0003g0128a0001c0001t0003g0151others(3): Show | 6 | HG02258.hp1 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.113-4525_113-4524d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432750 | ||||||
chr5:50432750
|
TA | T | 20 | a0001c0001t0001g0008a0001c0001t0001g0181a0001c0001t0001g0219others(17): Show | 23 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.113-4524delT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432750 | ||||||
chr5:50432772
|
C | T | 1 | a0001c0001t0003g0161 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.113-4545G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432772 | ||||||
chr5:50432906
|
G | A | 1 | a0001c0001t0004g0056 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.113-4679C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432906 | ||||||
chr5:50432927
|
A | T | 10 | a0001c0001t0002g0126a0001c0001t0007g0018a0001c0001t0007g0123others(7): Show | 11 | HG00735.hp1 HG00741.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.113-4700T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432927 | ||||||
chr5:50432929
|
T | A | 1 | a0001c0001t0001g0265 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.113-4702A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50432929 | ||||||
chr5:50433002
|
C | T | 1 | a0001c0004t0004g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.113-4775G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433002 | ||||||
chr5:50433100
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.113-4873A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433100 | ||||||
chr5:50433350
|
A | AG | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.113-5124_113-5123i others(3): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433350 | ||||||
chr5:50433373
|
C | T | 9 | a0001c0001t0005g0011a0001c0001t0005g0045a0001c0001t0005g0046others(6): Show | 10 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-5146G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433373 | ||||||
chr5:50433442
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.113-5215C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433442 | ||||||
chr5:50433600
|
T | C | 23 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0181others(20): Show | 26 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.113-5373A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433600 | ||||||
chr5:50433855
|
A | C | 1 | a0001c0001t0001g0189 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.113-5628T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433855 | ||||||
chr5:50433882
|
G | A | 1 | a0001c0001t0006g0175 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.113-5655C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433882 | ||||||
chr5:50433905
|
T | A | 1 | a0001c0001t0001g0164 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.113-5678A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433905 | ||||||
chr5:50433971
|
C | T | 1 | a0001c0001t0004g0056 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.113-5744G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50433971 | ||||||
chr5:50434057
|
T | C | 1 | a0001c0001t0004g0056 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.113-5830A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434057 | ||||||
chr5:50434260
|
C | A | 5 | a0001c0001t0004g0099a0001c0001t0005g0016a0001c0001t0005g0100others(2): Show | 6 | HG02109.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-6033G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434260 | ||||||
chr5:50434427
|
T | C | 176 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(173): Show | 208 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.113-6200A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434427 | ||||||
chr5:50434448
|
C | T | 1 | a0002c0003t0002g0086 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.113-6221G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434448 | ||||||
chr5:50434497
|
G | T | 148 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(145): Show | 176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.113-6270C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434497 | ||||||
chr5:50434509
|
T | G | 1 | a0002c0003t0002g0086 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.113-6282A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434509 | ||||||
chr5:50434594
|
G | C | 148 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(145): Show | 176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.113-6367C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434594 | ||||||
chr5:50434664
|
G | A | 7 | a0001c0001t0004g0010a0001c0001t0004g0039a0001c0001t0004g0040others(4): Show | 8 | HG01261.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+6376C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434664 | ||||||
chr5:50434672
|
T | C | 1 | a0001c0001t0004g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.112+6368A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434672 | ||||||
chr5:50434768
|
T | C | 1 | a0002c0003t0002g0087 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.112+6272A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50434768 | ||||||
chr5:50435055
|
A | T | 1 | a0001c0001t0006g0021 | 2 | HG02040.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.112+5985T>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435055 | ||||||
chr5:50435093
|
C | T | 1 | a0001c0001t0004g0160 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.112+5947G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435093 | ||||||
chr5:50435097
|
G | A | 7 | a0001c0001t0004g0049a0001c0001t0004g0056a0001c0001t0004g0061others(4): Show | 8 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+5943C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435097 | ||||||
chr5:50435175
|
A | G | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.112+5865T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435175 | ||||||
chr5:50435333
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.112+5707A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435333 | ||||||
chr5:50435352
|
C | T | 1 | a0001c0001t0005g0279 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.112+5688G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435352 | ||||||
chr5:50435414
|
C | A | 1 | a0001c0001t0004g0056 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.112+5626G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435414 | ||||||
chr5:50435423
|
G | A | 1 | a0001c0001t0007g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.112+5617C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435423 | ||||||
chr5:50435606
|
G | A | 9 | a0001c0001t0004g0099a0001c0001t0005g0016a0001c0001t0005g0065others(6): Show | 10 | HG02109.hp2 HG02280.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.112+5434C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435606 | ||||||
chr5:50435617
|
C | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0092 | 3 | HG02258.hp2 HG03209.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.112+5423G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435617 | ||||||
chr5:50435769
|
T | C | 1 | a0001c0001t0009g0089 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.112+5271A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435769 | ||||||
chr5:50435816
|
A | G | 1 | a0001c0001t0021g0097 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.112+5224T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435816 | ||||||
chr5:50435821
|
T | C | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | NA18939.hp2 NA18999.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.112+5219A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50435821 | ||||||
chr5:50436005
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.112+5035C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50436005 | ||||||
chr5:50436299
|
T | C | 1 | a0001c0001t0003g0009 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.112+4741A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50436299 | ||||||
chr5:50436379
|
A | G | 14 | a0001c0002t0004g0031a0001c0002t0004g0032a0001c0002t0004g0033others(11): Show | 18 | HG01109.hp2 HG01192.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.112+4661T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50436379 | ||||||
chr5:50436837
|
T | G | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.112+4203A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50436837 | ||||||
chr5:50436843
|
G | A | 13 | a0001c0001t0006g0021a0001c0001t0006g0022a0001c0001t0006g0116others(10): Show | 15 | HG00323.hp1 HG00558.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.112+4197C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50436843 | ||||||
chr5:50436932
|
T | C | 1 | a0001c0001t0006g0159 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.112+4108A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50436932 | ||||||
chr5:50436994
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.112+4046C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50436994 | ||||||
chr5:50437128
|
G | A | 7 | a0001c0001t0004g0010a0001c0001t0004g0039a0001c0001t0004g0040others(4): Show | 8 | HG01261.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+3912C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437128 | ||||||
chr5:50437152
|
T | C | 1 | a0001c0007t0029g0283 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.112+3888A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437152 | ||||||
chr5:50437294
|
G | A | 4 | a0001c0001t0004g0050a0001c0001t0010g0057a0001c0001t0010g0058others(1): Show | 4 | HG02145.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+3746C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437294 | ||||||
chr5:50437376
|
G | A | 1 | a0001c0001t0001g0028 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.112+3664C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437376 | ||||||
chr5:50437674
|
T | TGTCA | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(144): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.112+3362_112+3365d others(6): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437674 | ||||||
chr5:50437716
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.112+3324T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437716 | ||||||
chr5:50437800
|
C | T | 3 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0068 | 3 | HG02293.hp2 HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.112+3240G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437800 | ||||||
chr5:50437954
|
T | A | 3 | a0001c0001t0002g0014a0001c0001t0002g0090a0001c0001t0002g0091 | 4 | NA19003.hp1 NA19011.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+3086A>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437954 | ||||||
chr5:50437982
|
C | G | 2 | a0001c0001t0002g0060a0001c0001t0003g0009 | 3 | HG02486.hp1 HG03130.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.112+3058G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50437982 | ||||||
chr5:50438312
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.112+2728C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438312 | ||||||
chr5:50438380
|
G | C | 1 | a0001c0001t0004g0129 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.112+2660C>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438380 | ||||||
chr5:50438506
|
C | T | 1 | a0001c0001t0027g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.112+2534G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438506 | ||||||
chr5:50438513
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0022g0237 | 3 | HG02630.hp2 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.112+2527T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438513 | ||||||
chr5:50438589
|
T | C | 1 | a0001c0001t0001g0235 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.112+2451A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438589 | ||||||
chr5:50438605
|
T | C | 1 | a0001c0007t0029g0283 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.112+2435A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438605 | ||||||
chr5:50438631
|
A | C | 1 | a0001c0001t0001g0253 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.112+2409T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438631 | ||||||
chr5:50438668
|
T | C | 1 | a0001c0001t0005g0279 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.112+2372A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438668 | ||||||
chr5:50438671
|
C | G | 27 | a0001c0001t0004g0099a0001c0001t0005g0011a0001c0001t0005g0016others(24): Show | 31 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.112+2369G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438671 | ||||||
chr5:50438736
|
A | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0162a0001c0001t0001g0176 | 3 | HG02559.hp1 HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.112+2304T>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438736 | ||||||
chr5:50438766
|
T | C | 2 | a0001c0001t0002g0015a0001c0001t0002g0092 | 3 | HG02258.hp2 HG03209.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.112+2274A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438766 | ||||||
chr5:50438847
|
C | A | 1 | a0001c0001t0004g0160 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.112+2193G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438847 | ||||||
chr5:50438903
|
CT | C | 6 | a0001c0001t0002g0093a0001c0001t0003g0009a0001c0001t0003g0161others(3): Show | 7 | HG01192.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+2136delA | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438903 | ||||||
chr5:50438957
|
C | T | 3 | a0001c0001t0004g0099a0001c0001t0005g0100a0001c0001t0009g0051 | 3 | HG02109.hp2 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.112+2083G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50438957 | ||||||
chr5:50439252
|
C | T | 1 | a0001c0004t0004g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.112+1788G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439252 | ||||||
chr5:50439411
|
G | A | 3 | a0001c0001t0004g0094a0001c0001t0004g0095a0001c0001t0004g0113 | 3 | HG02615.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.112+1629C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439411 | ||||||
chr5:50439487
|
AT | A | 115 | a0001c0001t0001g0236a0001c0001t0001g0238a0001c0001t0001g0239others(112): Show | 139 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.112+1552delA | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439487 | ||||||
chr5:50439487
|
ATT | A | 67 | a0001c0001t0002g0096a0001c0001t0002g0114a0001c0001t0003g0009others(64): Show | 75 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.112+1551_112+1552d others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439487 | ||||||
chr5:50439536
|
G | A | 175 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(172): Show | 207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.112+1504C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439536 | ||||||
chr5:50439676
|
C | A | 175 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(172): Show | 207 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.112+1364G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439676 | ||||||
chr5:50439895
|
G | T | 5 | a0001c0001t0004g0050a0001c0001t0004g0061a0001c0001t0010g0057others(2): Show | 5 | HG01346.hp2 HG02145.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.112+1145C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439895 | ||||||
chr5:50439973
|
T | C | 1 | a0001c0004t0004g0035 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.112+1067A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50439973 | ||||||
chr5:50440086
|
C | A | 1 | a0001c0001t0001g0278 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.112+954G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440086 | ||||||
chr5:50440113
|
CAT | C | 3 | a0001c0001t0001g0253a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG02056.hp1 NA19055.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.112+925_112+926del others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440113 | ||||||
chr5:50440185
|
G | A | 3 | a0001c0001t0010g0057a0001c0001t0010g0058a0001c0001t0010g0059 | 3 | HG02145.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.112+855C>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440185 | ||||||
chr5:50440308
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.112+732G>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440308 | ||||||
chr5:50440337
|
C | G | 1 | a0001c0001t0004g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.112+703G>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440337 | ||||||
chr5:50440417
|
C | A | 1 | a0001c0001t0002g0060 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.112+623G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440417 | ||||||
chr5:50440533
|
C | CA | 24 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0030others(21): Show | 31 | HG00597.hp2 HG01070.hp2 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.112+506dupT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | ||||||
chr5:50440533
|
C | CAA | 7 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(4): Show | 7 | HG00558.hp2 HG00741.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.112+505_112+506dup others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | ||||||
chr5:50440533
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0005g0279 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.112+487_112+506dup others(20): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | ||||||
chr5:50440533
|
CA | C | 13 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(10): Show | 14 | HG00140.hp2 HG00738.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.112+506delT | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | ||||||
chr5:50440533
|
CAA | C | 14 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(11): Show | 14 | HG00323.hp1 HG00438.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.112+505_112+506del others(2): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | ||||||
chr5:50440533
|
CAAA | C | 52 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0120others(49): Show | 59 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.112+504_112+506del others(3): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | ||||||
chr5:50440533
|
CAAAA | C | 32 | a0001c0001t0001g0098a0001c0001t0002g0006a0001c0001t0002g0017others(29): Show | 39 | HG00438.hp2 HG00642.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.112+503_112+506del others(4): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | ||||||
chr5:50440533
|
CAAAAA | C | 55 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0012others(52): Show | 72 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.112+502_112+506del others(5): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | ||||||
chr5:50440533
|
CAAAAAA | C | 12 | a0001c0001t0002g0055a0001c0001t0002g0060a0001c0001t0004g0049others(9): Show | 12 | HG01167.hp2 HG01243.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.112+501_112+506del others(6): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | ||||||
chr5:50440533
|
CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0005g0011a0001c0001t0005g0045a0001c0001t0005g0046others(2): Show | 6 | HG00642.hp2 HG01074.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+499_112+506del others(8): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | ||||||
chr5:50440533
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0003g0044 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.112+497_112+506del others(10): Show |
EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440533 | ||||||
chr5:50440561
|
A | G | 6 | a0001c0001t0004g0010a0001c0001t0004g0039a0001c0001t0004g0040others(3): Show | 7 | HG01261.hp1 HG01891.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+479T>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440561 | ||||||
chr5:50440608
|
T | G | 1 | a0001c0001t0001g0280 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.112+432A>C | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440608 | ||||||
chr5:50440933
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.112+107A>G | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440933 | ||||||
chr5:50440957
|
C | A | 1 | a0001c0001t0001g0282 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.112+83G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440957 | ||||||
chr5:50440988
|
G | T | 1 | a0001c0001t0003g0009 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.112+52C>A | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50440988 | ||||||
chr5:50441018
|
C | A | 1 | a0001c0007t0029g0283 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.112+22G>T | EMB | ENSG00000170571.12 | transcript | ENST00000303221.10 | protein_coding | 1/8 | chr5 | 50441018 |