geneid | 29079 |
---|---|
ensemblid | ENSG00000136146.15 |
hgncid | 17903 |
symbol | MED4 |
name | mediator complex subunit 4 |
refseq_nuc | NM_014166.4 |
refseq_prot | NP_054885.1 |
ensembl_nuc | ENST00000258648.7 |
ensembl_prot | ENSP00000258648.2 |
mane_status | MANE Select |
chr | chr13 |
start | 48075724 |
end | 48095104 |
strand | - |
ver | v1.2 |
region | chr13:48075724-48095104 |
region5000 | chr13:48070724-48100104 |
regionname0 | MED4_chr13_48075724_48095104 |
regionname5000 | MED4_chr13_48070724_48100104 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 270 | 406 | 86 | 69 | 188 | 17 | 44 | 152 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0002 | 0/0 | 270 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0003 | 0/0 | 270 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 813 | 401 | 83 | 69 | 186 | 17 | 44 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
c0002 | 0/0 | 813 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
c0003 | 0/0 | 813 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
c0004 | 0/0 | 813 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
c0005 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
c0006 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1442 | 316 | 62 | 51 | 164 | 15 | 22 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0002 | 0/0 | 1441 | 30 | 12 | 3 | 15 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0003 | 0/0 | 1442 | 20 | 0 | 9 | 2 | 0 | 9 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0004 | 0/0 | 1438 | 16 | 0 | 3 | 2 | 1 | 10 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0005 | 0/0 | 1443 | 4 | 3 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0006 | 0/0 | 1438 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0007 | 0/0 | 1442 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0008 | 0/0 | 1442 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0009 | 0/0 | 1442 | 2 | 1 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0010 | 0/0 | 1442 | 2 | 0 | 1 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0011 | 0/0 | 1442 | 2 | 0 | 0 | 0 | 1 | 1 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0012 | 0/0 | 1441 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0013 | 0/0 | 1442 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0014 | 0/0 | 1442 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0015 | 0/0 | 1443 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0016 | 0/0 | 1442 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0017 | 0/0 | 1442 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0018 | 0/0 | 1442 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
t0019 | 0/0 | 1442 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 30 | 0 | 8 | 22 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0002 | 0/0 | 26 | 0 | 7 | 18 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0003 | 0/0 | 22 | 2 | 1 | 18 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0004 | 0/1 | 21 | 0 | 3 | 12 | 1 | 4 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0005 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0006 | 0/0 | 9 | 1 | 3 | 0 | 2 | 3 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0007 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0010 | 0/0 | 7 | 0 | 2 | 1 | 0 | 4 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0011 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0015 | 0/0 | 5 | 0 | 1 | 0 | 0 | 4 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0016 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0018 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0019 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0021 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0022 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0024 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0028 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0029 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0030 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0031 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0033 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0052 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 813 | 401 | 83 | 69 | 186 | 17 | 44 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0002 | 0/0 | 813 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0005 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0006 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0002c0004 | 0/0 | 813 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0003c0003 | 0/0 | 813 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2254 | 309 | 59 | 50 | 162 | 14 | 22 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0002 | 0/0 | 2253 | 30 | 12 | 3 | 15 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0003 | 0/0 | 2254 | 20 | 0 | 9 | 2 | 0 | 9 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0004 | 0/0 | 2250 | 16 | 0 | 3 | 2 | 1 | 10 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0005 | 0/0 | 2255 | 4 | 3 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0006 | 0/0 | 2250 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0007 | 0/0 | 2254 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0008 | 0/0 | 2254 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0009 | 0/0 | 2254 | 2 | 1 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0010 | 0/0 | 2254 | 2 | 0 | 1 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0011 | 0/0 | 2254 | 2 | 0 | 0 | 0 | 1 | 1 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0012 | 0/0 | 2253 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0013 | 0/0 | 2254 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0014 | 0/0 | 2254 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0015 | 0/0 | 2255 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0016 | 0/0 | 2254 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0017 | 0/0 | 2254 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0018 | 0/0 | 2254 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0001t0019 | 0/0 | 2254 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0002t0001 | 0/0 | 2254 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0005t0001 | 0/0 | 2254 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0001c0006t0001 | 0/0 | 2254 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0002c0004t0001 | 0/0 | 2254 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
a0003c0003t0001 | 0/0 | 2254 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | copy fasta | chr13 | 48070724 | 48100104 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 30 | 0 | 8 | 22 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0002 | 0/0 | 26 | 0 | 7 | 18 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0003 | 0/0 | 22 | 2 | 1 | 18 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0004 | 0/1 | 21 | 0 | 3 | 12 | 1 | 4 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0005 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0006 | 0/0 | 9 | 1 | 3 | 0 | 2 | 3 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0007 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0016 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0018 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0019 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0022 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0024 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0031 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0033 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0028 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0003g0010 | 0/0 | 7 | 0 | 2 | 1 | 0 | 4 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0003g0011 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0003g0030 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0004g0015 | 0/0 | 5 | 0 | 1 | 0 | 0 | 4 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0004g0021 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0004g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0007g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0008g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0009g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0010g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0010g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0011g0042 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0012g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0013g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0014g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0015g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0016g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0017g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0018g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0001t0019g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0002t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0005t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0001c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0002c0004t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0019 | g0181 | EUR | GBR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00099 | hp2 | a0003 | c0003 | t0001 | g0053 | EUR | GBR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | GBR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0165 | EUR | FIN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00280 | hp2 | a0001 | c0001 | t0011 | g0042 | EUR | FIN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG00741 | hp2 | a0002 | c0004 | t0001 | g0136 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0157 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01167 | hp1 | a0001 | c0001 | t0016 | g0127 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0049 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0046 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01433 | hp1 | a0001 | c0001 | t0012 | g0104 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01496 | hp1 | a0001 | c0001 | t0010 | g0137 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0166 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02080 | hp1 | a0001 | c0006 | t0001 | g0077 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02083 | hp2 | a0001 | c0001 | t0018 | g0119 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CDX | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0108 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0164 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0021 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0046 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02886 | hp2 | a0001 | c0001 | t0015 | g0114 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0040 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0049 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03041 | hp1 | a0001 | c0001 | t0013 | g0117 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0021 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0113 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0106 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0163 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0107 | AFR | GWD | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03654 | hp1 | a0001 | c0001 | t0011 | g0042 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03654 | hp2 | a0001 | c0001 | t0010 | g0168 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03669 | hp1 | a0001 | c0001 | t0014 | g0073 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0021 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0021 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0156 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | YRI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18978 | hp1 | a0001 | c0001 | t0008 | g0037 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18989 | hp1 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | LWK | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19054 | hp2 | a0001 | c0001 | t0008 | g0037 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19081 | hp1 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19084 | hp2 | a0001 | c0005 | t0001 | g0148 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19090 | hp2 | a0001 | c0001 | t0017 | g0125 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | YRI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | TSI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0015 | SAS | GIH | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | GIH | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | MSL | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | USA | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | USA | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0004 | REF | REF | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0162 | REF | REF | MED4_chr13_48070724_48100104 | MED4 | chr13 | 48070724 | 48100104 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:48077193
|
A | T | 1 | a0002 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.759T>A | p.Asp253Glu | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 785/2254 | 759/813 | 253/270 | chr13 | 48077193 | ||
chr13:48095045
|
C | G | 1 | a0003 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.34G>C | p.Glu12Gln | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/7 | 60/2254 | 34/813 | 12/270 | chr13 | 48095045 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:48081670
|
T | A | 1 | a0001c0002 | 3 | HG03130.hp1 HG03471.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.483A>T | p.Val161Val | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/7 | 509/2254 | 483/813 | 161/270 | chr13 | 48081670 | ||
chr13:48081688
|
G | A | 1 | a0001c0005 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.465C>T | p.Ile155Ile | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/7 | 491/2254 | 465/813 | 155/270 | chr13 | 48081688 | ||
chr13:48090382
|
T | C | 1 | a0001c0006 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.162A>G | p.Gln54Gln | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/7 | 188/2254 | 162/813 | 54/270 | chr13 | 48090382 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:48075838
|
C | T | 1 | a0001c0001t0015 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1301G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 1301 | chr13 | 48075838 | |||||
chr13:48075865
|
G | T | 4 | a0001c0001t0003a0001c0001t0009a0001c0001t0013others(1): Show | 24 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1274C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 1274 | chr13 | 48075865 | |||||
chr13:48075904
|
TCTC | T | 1 | a0001c0001t0006 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1232_*1234delGAG | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 1232 | chr13 | 48075904 | |||||
chr13:48076190
|
G | T | 1 | a0001c0001t0012 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*949C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 949 | chr13 | 48076190 | |||||
chr13:48076304
|
G | A | 1 | a0001c0001t0014 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*835C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 835 | chr13 | 48076304 | |||||
chr13:48076356
|
A | G | 2 | a0001c0001t0003a0001c0001t0018 | 21 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*783T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 783 | chr13 | 48076356 | |||||
chr13:48076358
|
A | C | 1 | a0001c0001t0006 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*781T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 781 | chr13 | 48076358 | |||||
chr13:48076565
|
T | TA | 2 | a0001c0001t0005a0001c0001t0015 | 5 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*573dupT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 573 | chr13 | 48076565 | |||||
chr13:48076565
|
TA | T | 3 | a0001c0001t0002a0001c0001t0006a0001c0001t0012 | 34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*573delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 573 | chr13 | 48076565 | |||||
chr13:48076585
|
TACAA | T | 1 | a0001c0001t0004 | 16 | HG00280.hp1 HG01069.hp1 HG01167.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*550_*553delTTGT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 550 | chr13 | 48076585 | |||||
chr13:48076660
|
A | G | 1 | a0001c0001t0008 | 2 | NA18978.hp1 NA19054.hp2 |
3_prime_UTR_variant | MODIFIER | c.*479T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 479 | chr13 | 48076660 | |||||
chr13:48076686
|
C | G | 3 | a0001c0001t0002a0001c0001t0006a0001c0001t0012 | 34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*453G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 453 | chr13 | 48076686 | |||||
chr13:48076709
|
C | T | 1 | a0001c0001t0007 | 3 | HG02622.hp1 HG02895.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*430G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 430 | chr13 | 48076709 | |||||
chr13:48076799
|
T | A | 1 | a0001c0001t0010 | 2 | HG01496.hp1 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*340A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 340 | chr13 | 48076799 | |||||
chr13:48076842
|
T | C | 1 | a0001c0001t0011 | 2 | HG00280.hp2 HG03654.hp1 |
3_prime_UTR_variant | MODIFIER | c.*297A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 297 | chr13 | 48076842 | |||||
chr13:48076883
|
G | A | 1 | a0001c0001t0016 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*256C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 256 | chr13 | 48076883 | |||||
chr13:48077037
|
T | C | 1 | a0001c0001t0017 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*102A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 102 | chr13 | 48077037 | |||||
chr13:48077104
|
A | C | 4 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(1): Show | 35 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*35T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 35 | chr13 | 48077104 | |||||
chr13:48077124
|
G | A | 1 | a0001c0001t0018 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 7/7 | 15 | chr13 | 48077124 | |||||
chr13:48095098
|
C | A | 1 | a0001c0001t0019 | 1 | HG00099.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-20G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/7 | chr13 | 48095098 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:48077336
|
A | G | 1 | a0001c0001t0002g0100 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.641-25T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48077336 | ||||||
chr13:48077381
|
T | C | 3 | a0001c0001t0006g0106a0001c0001t0006g0107a0001c0001t0006g0108 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.641-70A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48077381 | ||||||
chr13:48077701
|
G | A | 9 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0030others(6): Show | 23 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.641-390C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48077701 | ||||||
chr13:48077805
|
T | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0112 | 6 | HG01884.hp1 HG02055.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.641-494A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48077805 | ||||||
chr13:48077879
|
T | C | 10 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0030others(7): Show | 24 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.641-568A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48077879 | ||||||
chr13:48077963
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(63): Show | 166 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.641-652G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48077963 | ||||||
chr13:48078069
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.641-758T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078069 | ||||||
chr13:48078216
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 12 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.641-905C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078216 | ||||||
chr13:48078223
|
T | C | 20 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(17): Show | 31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.641-912A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078223 | ||||||
chr13:48078251
|
C | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.641-940G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078251 | ||||||
chr13:48078281
|
AACCATTT | A | 20 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(17): Show | 31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.641-977_641-971del others(7): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078281 | ||||||
chr13:48078454
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.641-1143C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078454 | ||||||
chr13:48078460
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0151 | 3 | HG00544.hp2 NA18949.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.641-1149C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078460 | ||||||
chr13:48078645
|
T | C | 5 | a0001c0001t0002g0039a0001c0001t0002g0093a0001c0001t0002g0096others(2): Show | 6 | HG02723.hp2 HG02965.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.640+1199A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078645 | ||||||
chr13:48078646
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0068others(4): Show | 17 | HG00438.hp2 HG02071.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.640+1198T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078646 | ||||||
chr13:48078692
|
G | T | 1 | a0001c0001t0001g0124 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.640+1152C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078692 | ||||||
chr13:48078779
|
T | C | 10 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0030others(7): Show | 24 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.640+1065A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078779 | ||||||
chr13:48078838
|
A | G | 1 | a0001c0001t0001g0020 | 4 | NA18971.hp2 NA18977.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+1006T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078838 | ||||||
chr13:48078860
|
G | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0050others(7): Show | 21 | HG00140.hp2 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.640+984C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078860 | ||||||
chr13:48078912
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 12 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.640+932T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48078912 | ||||||
chr13:48079032
|
C | A | 1 | a0001c0001t0001g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.640+812G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079032 | ||||||
chr13:48079032
|
C | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0050others(7): Show | 21 | HG00140.hp2 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.640+812G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079032 | ||||||
chr13:48079160
|
A | G | 8 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0030others(5): Show | 21 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.640+684T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079160 | ||||||
chr13:48079278
|
T | C | 1 | a0001c0001t0005g0164 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.640+566A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079278 | ||||||
chr13:48079460
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0050a0001c0001t0001g0176others(1): Show | 10 | NA18944.hp2 NA18954.hp1 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.640+384C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079460 | ||||||
chr13:48079518
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.640+326A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079518 | ||||||
chr13:48079582
|
A | C | 1 | a0001c0001t0005g0166 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.640+262T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079582 | ||||||
chr13:48079633
|
G | T | 1 | a0001c0001t0001g0074 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.640+211C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079633 | ||||||
chr13:48079680
|
G | A | 23 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.640+164C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079680 | ||||||
chr13:48079728
|
CA | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(56): Show | 146 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.640+115delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079728 | ||||||
chr13:48079742
|
T | A | 1 | a0001c0001t0002g0105 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.640+102A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079742 | ||||||
chr13:48079821
|
AAC | A | 9 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0030others(6): Show | 23 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.640+21_640+22delGT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 6/6 | chr13 | 48079821 | ||||||
chr13:48080031
|
T | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG01074.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.509-56A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080031 | ||||||
chr13:48080204
|
C | CT | 4 | a0001c0001t0001g0006a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 12 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.509-230dupA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080204 | ||||||
chr13:48080225
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.509-250G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080225 | ||||||
chr13:48080268
|
G | A | 1 | a0001c0001t0015g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.509-293C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080268 | ||||||
chr13:48080286
|
A | G | 3 | a0001c0001t0006g0106a0001c0001t0006g0107a0001c0001t0006g0108 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.509-311T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080286 | ||||||
chr13:48080319
|
C | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.509-344G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080319 | ||||||
chr13:48080350
|
T | C | 3 | a0001c0001t0006g0106a0001c0001t0006g0107a0001c0001t0006g0108 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.509-375A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080350 | ||||||
chr13:48080390
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(63): Show | 166 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.509-415G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080390 | ||||||
chr13:48080396
|
C | CA | 67 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 164 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.509-422dupT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080396 | ||||||
chr13:48080396
|
C | CAA | 20 | a0001c0001t0001g0041a0001c0001t0001g0065a0001c0001t0001g0134others(17): Show | 33 | HG00558.hp1 HG01069.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.509-423_509-422dup others(2): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080396 | ||||||
chr13:48080396
|
C | CAAA | 8 | a0001c0001t0001g0147a0001c0001t0001g0170a0001c0001t0002g0039others(5): Show | 9 | HG01515.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.509-424_509-422dup others(3): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080396 | ||||||
chr13:48080396
|
CA | C | 6 | a0001c0001t0001g0025a0001c0001t0001g0050a0001c0001t0001g0062others(3): Show | 9 | HG01069.hp1 HG01975.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-422delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080396 | ||||||
chr13:48080415
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.509-440T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080415 | ||||||
chr13:48080469
|
T | C | 1 | a0001c0001t0002g0039 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.509-494A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080469 | ||||||
chr13:48080486
|
G | T | 1 | a0001c0001t0001g0024 | 3 | HG01515.hp2 HG01517.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.509-511C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080486 | ||||||
chr13:48080534
|
C | T | 2 | a0001c0001t0007g0040a0001c0001t0007g0113 | 3 | HG02622.hp1 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.509-559G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080534 | ||||||
chr13:48080613
|
T | C | 1 | a0001c0001t0015g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.509-638A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080613 | ||||||
chr13:48080701
|
G | A | 10 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0030others(7): Show | 24 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.509-726C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080701 | ||||||
chr13:48080741
|
C | CTT | 23 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.509-768_509-767dup others(2): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080741 | ||||||
chr13:48080741
|
CT | C | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(57): Show | 147 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.509-767delA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080741 | ||||||
chr13:48080994
|
C | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.508+651G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080994 | ||||||
chr13:48080998
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.508+647A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48080998 | ||||||
chr13:48081611
|
C | T | 1 | a0001c0001t0015g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.508+34G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 5/6 | chr13 | 48081611 | ||||||
chr13:48081940
|
A | G | 20 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(17): Show | 31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.422-209T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48081940 | ||||||
chr13:48081953
|
G | A | 3 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0166 | 3 | HG01891.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.422-222C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48081953 | ||||||
chr13:48081997
|
C | T | 23 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.422-266G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48081997 | ||||||
chr13:48082130
|
C | A | 1 | a0001c0001t0015g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.422-399G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082130 | ||||||
chr13:48082185
|
G | GT | 10 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0124others(7): Show | 41 | HG00323.hp2 HG00558.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.422-455dupA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082185 | ||||||
chr13:48082229
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.422-498G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082229 | ||||||
chr13:48082243
|
T | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(8): Show | 40 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.422-512A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082243 | ||||||
chr13:48082296
|
GA | G | 21 | a0001c0001t0001g0085a0001c0001t0002g0009a0001c0001t0002g0027others(18): Show | 32 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.422-566delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082296 | ||||||
chr13:48082404
|
G | GT | 2 | a0001c0001t0001g0023a0001c0001t0001g0067 | 4 | HG02258.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.422-674dupA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082404 | ||||||
chr13:48082417
|
G | A | 23 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.422-686C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082417 | ||||||
chr13:48082439
|
A | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(8): Show | 40 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.422-708T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082439 | ||||||
chr13:48082520
|
A | T | 1 | a0001c0001t0007g0113 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.422-789T>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082520 | ||||||
chr13:48082565
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.421+806A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082565 | ||||||
chr13:48082605
|
A | G | 1 | a0001c0001t0011g0042 | 2 | HG00280.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.421+766T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082605 | ||||||
chr13:48082684
|
G | A | 1 | a0001c0001t0001g0045 | 2 | NA18977.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.421+687C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082684 | ||||||
chr13:48082718
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.421+653A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082718 | ||||||
chr13:48082739
|
G | A | 1 | a0001c0001t0001g0020 | 4 | NA18971.hp2 NA18977.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+632C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082739 | ||||||
chr13:48082741
|
GGC | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0066 | 4 | HG01975.hp1 HG02615.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+628_421+629del others(2): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082741 | ||||||
chr13:48082757
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(8): Show | 40 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.421+614C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082757 | ||||||
chr13:48082826
|
C | CA | 14 | a0001c0001t0001g0128a0001c0001t0001g0131a0001c0001t0001g0167others(11): Show | 22 | HG00280.hp1 HG01069.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.421+544dupT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082826 | ||||||
chr13:48082826
|
CA | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(93): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.421+544delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 4/6 | chr13 | 48082826 | ||||||
chr13:48083447
|
A | T | 1 | a0001c0001t0001g0043 | 2 | NA18966.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.364-19T>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083447 | ||||||
chr13:48083551
|
A | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0130 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.364-123T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083551 | ||||||
chr13:48083625
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.364-197A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083625 | ||||||
chr13:48083656
|
T | C | 3 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0166 | 3 | HG01891.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.364-228A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083656 | ||||||
chr13:48083697
|
G | A | 27 | a0001c0001t0001g0167a0001c0001t0002g0009a0001c0001t0002g0027others(24): Show | 38 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(35): Show |
intron_variant | MODIFIER | c.364-269C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083697 | ||||||
chr13:48083786
|
C | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(53): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.364-358G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083786 | ||||||
chr13:48083843
|
A | G | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | HG01192.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.364-415T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083843 | ||||||
chr13:48083931
|
T | C | 8 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0138others(5): Show | 13 | HG00099.hp1 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.364-503A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48083931 | ||||||
chr13:48084052
|
G | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.364-624C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084052 | ||||||
chr13:48084079
|
G | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0050others(7): Show | 21 | HG00140.hp2 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.364-651C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084079 | ||||||
chr13:48084136
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.364-708C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084136 | ||||||
chr13:48084195
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.364-767C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084195 | ||||||
chr13:48084265
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0006g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.364-850_364-838dup others(13): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084265 | ||||||
chr13:48084265
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0006g0107 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.364-838_364-837ins others(26): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084265 | ||||||
chr13:48084265
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0006g0108 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.364-838_364-837ins others(27): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084265 | ||||||
chr13:48084265
|
CA | C | 17 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(14): Show | 28 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.364-838delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084265 | ||||||
chr13:48084265
|
CAAAA | C | 6 | a0001c0001t0004g0015a0001c0001t0004g0021a0001c0001t0004g0046others(3): Show | 14 | HG00280.hp1 HG01069.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.364-841_364-838del others(4): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084265 | ||||||
chr13:48084265
|
CAAAAAA | C | 59 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 129 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.364-843_364-838del others(6): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084265 | ||||||
chr13:48084265
|
CAAAAAAA | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(78): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.364-844_364-838del others(7): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084265 | ||||||
chr13:48084371
|
G | C | 1 | a0001c0001t0015g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.364-943C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084371 | ||||||
chr13:48084389
|
C | T | 23 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.364-961G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084389 | ||||||
chr13:48084415
|
G | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.364-987C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084415 | ||||||
chr13:48084470
|
CTCAA | C | 3 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0166 | 3 | HG01891.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.364-1046_364-1043d others(6): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084470 | ||||||
chr13:48084599
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.364-1171C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084599 | ||||||
chr13:48084770
|
G | A | 1 | a0001c0001t0002g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.364-1342C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084770 | ||||||
chr13:48084799
|
G | GT | 2 | a0001c0001t0001g0032a0001c0001t0001g0122 | 4 | NA18948.hp1 NA18948.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1372dupA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084799 | ||||||
chr13:48084811
|
T | C | 1 | a0001c0001t0009g0049 | 2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.364-1383A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084811 | ||||||
chr13:48084858
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(53): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.363+1424A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084858 | ||||||
chr13:48084959
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 12 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.363+1323G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084959 | ||||||
chr13:48084960
|
G | A | 4 | a0001c0001t0001g0013a0001c0001t0001g0070a0001c0001t0001g0075others(1): Show | 8 | HG02071.hp2 HG02080.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.363+1322C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084960 | ||||||
chr13:48084995
|
T | C | 1 | a0001c0001t0003g0120 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.363+1287A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48084995 | ||||||
chr13:48085011
|
C | T | 1 | a0001c0001t0002g0099 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.363+1271G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085011 | ||||||
chr13:48085012
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(53): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.363+1270C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085012 | ||||||
chr13:48085060
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.363+1222C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085060 | ||||||
chr13:48085074
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0070a0001c0006t0001g0077 | 7 | HG02071.hp2 HG02080.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+1208C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085074 | ||||||
chr13:48085158
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.363+1124A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085158 | ||||||
chr13:48085170
|
A | AT | 19 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0055others(16): Show | 31 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.363+1111dupA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085170 | ||||||
chr13:48085170
|
AT | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0062others(9): Show | 17 | HG01243.hp2 HG01975.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.363+1111delA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085170 | ||||||
chr13:48085170
|
ATT | A | 22 | a0001c0001t0001g0067a0001c0001t0001g0178a0001c0001t0002g0009others(19): Show | 34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.363+1110_363+1111d others(4): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085170 | ||||||
chr13:48085170
|
ATTTTTTT others(4): Show |
A | 8 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0030others(5): Show | 21 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.363+1101_363+1111d others(13): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085170 | ||||||
chr13:48085170
|
ATTTTTTT others(6): Show |
A | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(53): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.363+1099_363+1111d others(15): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085170 | ||||||
chr13:48085235
|
A | C | 1 | a0001c0001t0001g0174 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.363+1047T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085235 | ||||||
chr13:48085252
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0121 | 4 | HG01123.hp2 HG03710.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+1030T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085252 | ||||||
chr13:48085374
|
T | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(7): Show | 39 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.363+908A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085374 | ||||||
chr13:48085551
|
T | G | 1 | a0001c0001t0001g0139 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.363+731A>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085551 | ||||||
chr13:48085753
|
T | C | 1 | a0001c0001t0002g0039 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.363+529A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085753 | ||||||
chr13:48085943
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0038 | 5 | HG01106.hp2 HG01515.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+339C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085943 | ||||||
chr13:48085946
|
C | CA | 6 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0004g0157others(3): Show | 7 | HG00280.hp2 HG01069.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+335dupT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48085946 | ||||||
chr13:48086244
|
T | C | 10 | a0001c0001t0003g0010a0001c0001t0003g0011a0001c0001t0003g0030others(7): Show | 24 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.363+38A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48086244 | ||||||
chr13:48086267
|
CCT | C | 3 | a0001c0001t0005g0163a0001c0001t0005g0164a0001c0001t0005g0166 | 3 | HG01891.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.363+13_363+14delAG | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 3/6 | chr13 | 48086267 | ||||||
chr13:48086547
|
A | G | 20 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(17): Show | 31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.193-95T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086547 | ||||||
chr13:48086673
|
C | A | 1 | a0001c0001t0004g0165 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.193-221G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086673 | ||||||
chr13:48086717
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.193-265C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086717 | ||||||
chr13:48086728
|
G | C | 1 | a0001c0001t0001g0024 | 3 | HG01515.hp2 HG01517.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.193-276C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086728 | ||||||
chr13:48086784
|
T | C | 1 | a0001c0001t0001g0036 | 2 | HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.193-332A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086784 | ||||||
chr13:48086821
|
G | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0138others(5): Show | 13 | HG00099.hp1 HG00738.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.193-369C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086821 | ||||||
chr13:48086841
|
C | G | 3 | a0001c0001t0006g0106a0001c0001t0006g0107a0001c0001t0006g0108 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.193-389G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086841 | ||||||
chr13:48086841
|
C | T | 1 | a0001c0001t0002g0098 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.193-389G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086841 | ||||||
chr13:48086904
|
G | C | 1 | a0001c0001t0015g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.193-452C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086904 | ||||||
chr13:48086918
|
C | T | 3 | a0001c0001t0006g0106a0001c0001t0006g0107a0001c0001t0006g0108 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.193-466G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086918 | ||||||
chr13:48086983
|
T | C | 10 | a0001c0001t0002g0009a0001c0001t0002g0028a0001c0001t0002g0098others(7): Show | 18 | HG00558.hp1 HG01433.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.193-531A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086983 | ||||||
chr13:48086993
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.193-541G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48086993 | ||||||
chr13:48087024
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.193-572A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087024 | ||||||
chr13:48087104
|
G | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(57): Show | 147 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.193-652C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087104 | ||||||
chr13:48087180
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.193-728T>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087180 | ||||||
chr13:48087226
|
G | A | 1 | a0001c0001t0001g0019 | 4 | HG01099.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-774C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087226 | ||||||
chr13:48087289
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(9): Show | 41 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.193-837G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087289 | ||||||
chr13:48087321
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0112 | 6 | HG01884.hp1 HG02055.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-869C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087321 | ||||||
chr13:48087402
|
C | G | 20 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(17): Show | 31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.193-950G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087402 | ||||||
chr13:48087575
|
G | C | 1 | a0001c0001t0002g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.193-1123C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087575 | ||||||
chr13:48087594
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.193-1142C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087594 | ||||||
chr13:48087617
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.193-1165G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087617 | ||||||
chr13:48087678
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.193-1226G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087678 | ||||||
chr13:48087782
|
G | A | 1 | a0001c0001t0002g0102 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.193-1330C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087782 | ||||||
chr13:48087858
|
A | G | 1 | a0001c0001t0003g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.193-1406T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087858 | ||||||
chr13:48087975
|
C | G | 1 | a0001c0001t0015g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.193-1523G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48087975 | ||||||
chr13:48088187
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.193-1735T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088187 | ||||||
chr13:48088374
|
T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 140 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.193-1922A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088374 | ||||||
chr13:48088459
|
T | C | 10 | a0001c0001t0002g0009a0001c0001t0002g0028a0001c0001t0002g0098others(7): Show | 18 | HG00558.hp1 HG01433.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.192+1893A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088459 | ||||||
chr13:48088519
|
G | C | 3 | a0001c0001t0006g0106a0001c0001t0006g0107a0001c0001t0006g0108 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.192+1833C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088519 | ||||||
chr13:48088574
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.192+1778G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088574 | ||||||
chr13:48088738
|
T | C | 3 | a0001c0001t0006g0106a0001c0001t0006g0107a0001c0001t0006g0108 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.192+1614A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088738 | ||||||
chr13:48088788
|
T | A | 1 | a0001c0001t0001g0140 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.192+1564A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088788 | ||||||
chr13:48088952
|
A | C | 7 | a0001c0001t0004g0015a0001c0001t0004g0021a0001c0001t0004g0046others(4): Show | 15 | HG00280.hp1 HG01069.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.192+1400T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088952 | ||||||
chr13:48088958
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.192+1394C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088958 | ||||||
chr13:48088985
|
T | A | 1 | a0001c0001t0001g0141 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.192+1367A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48088985 | ||||||
chr13:48089030
|
A | C | 1 | a0001c0001t0001g0142 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.192+1322T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089030 | ||||||
chr13:48089043
|
G | C | 1 | a0001c0001t0011g0042 | 2 | HG00280.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.192+1309C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089043 | ||||||
chr13:48089066
|
C | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(57): Show | 147 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.192+1286G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089066 | ||||||
chr13:48089107
|
T | G | 2 | a0001c0001t0005g0163a0001c0001t0005g0164 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.192+1245A>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089107 | ||||||
chr13:48089188
|
GA | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.192+1163delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089188 | ||||||
chr13:48089222
|
A | G | 20 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(17): Show | 31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.192+1130T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089222 | ||||||
chr13:48089274
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.192+1078A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089274 | ||||||
chr13:48089352
|
G | A | 1 | a0001c0001t0002g0102 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.192+1000C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089352 | ||||||
chr13:48089541
|
A | T | 3 | a0001c0001t0006g0106a0001c0001t0006g0107a0001c0001t0006g0108 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.192+811T>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089541 | ||||||
chr13:48089589
|
A | C | 41 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(38): Show | 92 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.192+763T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089589 | ||||||
chr13:48089638
|
G | T | 20 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(17): Show | 31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.192+714C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089638 | ||||||
chr13:48089700
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.192+652A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089700 | ||||||
chr13:48089822
|
G | A | 4 | a0001c0001t0002g0028a0001c0001t0002g0103a0001c0001t0002g0105others(1): Show | 6 | HG01433.hp1 HG01943.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+530C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089822 | ||||||
chr13:48089948
|
T | C | 1 | a0001c0002t0001g0161 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.192+404A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48089948 | ||||||
chr13:48090204
|
A | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.192+148T>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48090204 | ||||||
chr13:48090313
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.192+39T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48090313 | ||||||
chr13:48090332
|
T | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0065others(2): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+20A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 2/6 | chr13 | 48090332 | ||||||
chr13:48090420
|
T | TA | 7 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0112others(4): Show | 7 | HG00140.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.126-3dupT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48090420 | ||||||
chr13:48090420
|
TA | T | 23 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
splice_region_variant&intron_variant | LOW | c.126-3delT | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48090420 | ||||||
chr13:48090498
|
T | C | 3 | a0001c0001t0006g0106a0001c0001t0006g0107a0001c0001t0006g0108 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.126-80A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48090498 | ||||||
chr13:48090630
|
G | C | 20 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(17): Show | 31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.126-212C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48090630 | ||||||
chr13:48090822
|
T | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(63): Show | 166 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.126-404A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48090822 | ||||||
chr13:48090837
|
G | A | 1 | a0001c0001t0001g0052 | 2 | HG00140.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.126-419C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48090837 | ||||||
chr13:48090982
|
T | G | 1 | a0001c0001t0001g0036 | 2 | HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.126-564A>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48090982 | ||||||
chr13:48091000
|
T | C | 2 | a0001c0001t0004g0021a0001c0001t0004g0165 | 5 | HG00280.hp1 HG02735.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.126-582A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091000 | ||||||
chr13:48091010
|
A | T | 1 | a0001c0001t0001g0142 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.126-592T>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091010 | ||||||
chr13:48091040
|
G | A | 21 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0032others(18): Show | 46 | HG00544.hp2 HG01346.hp2 HG01361.hp1 others(43): Show |
intron_variant | MODIFIER | c.126-622C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091040 | ||||||
chr13:48091076
|
T | C | 1 | a0001c0001t0005g0166 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126-658A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091076 | ||||||
chr13:48091222
|
T | A | 19 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(16): Show | 30 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.126-804A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091222 | ||||||
chr13:48091271
|
T | C | 2 | a0001c0001t0007g0040a0001c0001t0007g0113 | 3 | HG02622.hp1 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.126-853A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091271 | ||||||
chr13:48091280
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.126-862C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091280 | ||||||
chr13:48091473
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.126-1055A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091473 | ||||||
chr13:48091532
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.126-1114C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091532 | ||||||
chr13:48091578
|
T | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0013others(17): Show | 55 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.126-1160A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091578 | ||||||
chr13:48091768
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.126-1350A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091768 | ||||||
chr13:48091869
|
G | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(57): Show | 147 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.126-1451C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091869 | ||||||
chr13:48091920
|
T | A | 1 | a0001c0001t0002g0109 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.126-1502A>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48091920 | ||||||
chr13:48092002
|
C | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.126-1584G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092002 | ||||||
chr13:48092064
|
G | A | 20 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(17): Show | 31 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.126-1646C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092064 | ||||||
chr13:48092176
|
C | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0050others(7): Show | 21 | HG00140.hp2 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.126-1758G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092176 | ||||||
chr13:48092281
|
AT | A | 23 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.126-1864delA | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092281 | ||||||
chr13:48092306
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 12 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.126-1888A>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092306 | ||||||
chr13:48092354
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 12 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.126-1936G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092354 | ||||||
chr13:48092357
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG01074.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.126-1939G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092357 | ||||||
chr13:48092554
|
G | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(57): Show | 147 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.126-2136C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092554 | ||||||
chr13:48092625
|
C | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.126-2207G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092625 | ||||||
chr13:48092645
|
C | A | 3 | a0001c0001t0006g0106a0001c0001t0006g0107a0001c0001t0006g0108 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.126-2227G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092645 | ||||||
chr13:48092646
|
A | C | 3 | a0001c0001t0006g0106a0001c0001t0006g0107a0001c0001t0006g0108 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.126-2228T>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092646 | ||||||
chr13:48092655
|
A | T | 1 | a0001c0001t0015g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.126-2237T>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092655 | ||||||
chr13:48092692
|
G | A | 43 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(40): Show | 96 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.125+2262C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092692 | ||||||
chr13:48092762
|
G | A | 1 | a0001c0001t0009g0049 | 2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.125+2192C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092762 | ||||||
chr13:48092842
|
G | C | 3 | a0001c0001t0006g0106a0001c0001t0006g0107a0001c0001t0006g0108 | 3 | HG02572.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.125+2112C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092842 | ||||||
chr13:48092888
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.125+2066C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48092888 | ||||||
chr13:48093137
|
G | A | 1 | a0001c0001t0010g0168 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.125+1817C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48093137 | ||||||
chr13:48093261
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.125+1693C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48093261 | ||||||
chr13:48093561
|
CAT | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 12 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.125+1391_125+1392d others(4): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48093561 | ||||||
chr13:48093742
|
C | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(90): Show | 202 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(199): Show |
intron_variant | MODIFIER | c.125+1212G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48093742 | ||||||
chr13:48093788
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.125+1166C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48093788 | ||||||
chr13:48093882
|
G | A | 33 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0050others(30): Show | 55 | HG00140.hp2 HG00558.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.125+1072C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48093882 | ||||||
chr13:48094016
|
G | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0180 | 4 | HG00738.hp1 HG01168.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.125+938C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094016 | ||||||
chr13:48094131
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(9): Show | 41 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.125+823G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094131 | ||||||
chr13:48094253
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.125+701C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094253 | ||||||
chr13:48094274
|
A | G | 44 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(41): Show | 97 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.125+680T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094274 | ||||||
chr13:48094336
|
G | C | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.125+618C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094336 | ||||||
chr13:48094415
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.125+539G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094415 | ||||||
chr13:48094491
|
G | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0026others(7): Show | 39 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.125+463C>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094491 | ||||||
chr13:48094494
|
G | C | 1 | a0001c0001t0003g0173 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.125+460C>G | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094494 | ||||||
chr13:48094613
|
G | GTC | 10 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0050others(7): Show | 21 | HG00140.hp2 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.125+339_125+340dup others(2): Show |
MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094613 | ||||||
chr13:48094656
|
G | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(57): Show | 147 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.125+298C>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094656 | ||||||
chr13:48094678
|
A | G | 23 | a0001c0001t0002g0009a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 34 | HG00558.hp1 HG01069.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.125+276T>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094678 | ||||||
chr13:48094746
|
C | G | 1 | a0001c0001t0001g0091 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.125+208G>C | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094746 | ||||||
chr13:48094851
|
C | A | 1 | a0001c0001t0002g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.125+103G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094851 | ||||||
chr13:48094928
|
C | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(51): Show | 136 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.125+26G>A | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094928 | ||||||
chr13:48094937
|
C | A | 1 | a0001c0001t0001g0180 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.125+17G>T | MED4 | ENSG00000136146.15 | transcript | ENST00000258648.7 | protein_coding | 1/6 | chr13 | 48094937 |