geneid | 1876 |
---|---|
ensemblid | ENSG00000169016.17 |
hgncid | 3120 |
symbol | E2F6 |
name | E2F transcription factor 6 |
refseq_nuc | NM_198256.4 |
refseq_prot | NP_937987.2 |
ensembl_nuc | ENST00000381525.8 |
ensembl_prot | ENSP00000370936.3 |
mane_status | MANE Select |
chr | chr2 |
start | 11444375 |
end | 11466161 |
strand | - |
ver | v1.2 |
region | chr2:11444375-11466161 |
region5000 | chr2:11439375-11471161 |
regionname0 | E2F6_chr2_11444375_11466161 |
regionname5000 | E2F6_chr2_11439375_11471161 |
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 | 281 | 366 | 88 | 74 | 156 | 10 | 36 | 130 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
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 | 846 | 366 | 88 | 74 | 156 | 10 | 36 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
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 | 1/0 | 2385 | 167 | 41 | 44 | 61 | 4 | 16 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0002 | 0/1 | 2385 | 125 | 7 | 24 | 71 | 5 | 17 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0003 | 0/0 | 2385 | 27 | 25 | 2 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0004 | 0/0 | 2385 | 12 | 0 | 1 | 11 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0005 | 0/0 | 2384 | 9 | 0 | 0 | 9 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0006 | 0/0 | 2385 | 5 | 4 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0007 | 0/0 | 2385 | 4 | 4 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0008 | 0/0 | 2385 | 3 | 3 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0009 | 0/0 | 2385 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0010 | 0/0 | 2385 | 2 | 0 | 1 | 0 | 1 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0011 | 0/0 | 2385 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0012 | 0/0 | 2385 | 2 | 0 | 0 | 0 | 0 | 2 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0013 | 0/0 | 2385 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0014 | 0/0 | 2385 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0015 | 0/0 | 2385 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0016 | 0/0 | 2385 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0017 | 0/0 | 2385 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
t0018 | 0/0 | 2385 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
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 | 28 | 0 | 8 | 19 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0002 | 0/0 | 21 | 2 | 2 | 13 | 2 | 2 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0003 | 0/0 | 15 | 0 | 5 | 9 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0004 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0007 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0012 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0020 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0025 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0027 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0028 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0029 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0051 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
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 | 846 | 366 | 88 | 74 | 156 | 10 | 36 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3230 | 167 | 41 | 44 | 61 | 4 | 16 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0002 | 0/1 | 3230 | 125 | 7 | 24 | 71 | 5 | 17 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0003 | 0/0 | 3230 | 27 | 25 | 2 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0004 | 0/0 | 3230 | 12 | 0 | 1 | 11 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0005 | 0/0 | 3229 | 9 | 0 | 0 | 9 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0006 | 0/0 | 3230 | 5 | 4 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0007 | 0/0 | 3230 | 4 | 4 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0008 | 0/0 | 3230 | 3 | 3 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0009 | 0/0 | 3230 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0010 | 0/0 | 3230 | 2 | 0 | 1 | 0 | 1 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0011 | 0/0 | 3230 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0012 | 0/0 | 3230 | 2 | 0 | 0 | 0 | 0 | 2 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0013 | 0/0 | 3230 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0014 | 0/0 | 3230 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0015 | 0/0 | 3230 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0016 | 0/0 | 3230 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0017 | 0/0 | 3230 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
a0001c0001t0018 | 0/0 | 3230 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | copy fasta | chr2 | 11439375 | 11471161 |
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 | 28 | 0 | 8 | 19 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0020 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0002 | 0/0 | 21 | 2 | 2 | 13 | 2 | 2 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0003 | 0/0 | 15 | 0 | 5 | 9 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0012 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0025 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0027 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0028 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0004g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0004g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0005g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0005g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0006g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0007g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0010g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0010g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0011g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0012g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0012g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0013g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0014g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0015g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0016g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0017g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
a0001c0001t0018g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | GBR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0061 | EUR | GBR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | CHS | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00639 | hp1 | a0001 | c0001 | t0016 | g0178 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01070 | hp1 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01167 | hp1 | a0001 | c0001 | t0010 | g0055 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0028 | EUR | IBS | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0205 | EUR | IBS | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0139 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | KHV | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | KHV | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0198 | EAS | KHV | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | CDX | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02451 | hp2 | a0001 | c0001 | t0009 | g0053 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0081 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0058 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0084 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0052 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0054 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | MSL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0052 | AFR | MSL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0057 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | MSL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | MSL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | MSL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03654 | hp2 | a0001 | c0001 | t0012 | g0154 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | STU | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | BEB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03927 | hp2 | a0001 | c0001 | t0014 | g0152 | SAS | BEB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | BEB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG04115 | hp1 | a0001 | c0001 | t0012 | g0153 | SAS | STU | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | STU | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | STU | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | YRI | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18612 | hp2 | a0001 | c0001 | t0013 | g0166 | EAS | CHB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | YRI | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0101 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18946 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18965 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18970 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18971 | hp2 | a0001 | c0001 | t0015 | g0110 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18989 | hp2 | a0001 | c0001 | t0011 | g0041 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18991 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19043 | hp2 | a0001 | c0001 | t0017 | g0209 | AFR | LWK | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19090 | hp2 | a0001 | c0001 | t0011 | g0041 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ASW | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | ASW | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA20805 | hp2 | a0001 | c0001 | t0010 | g0056 | EUR | TSI | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | GIH | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | GIH | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | MSL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG06807 | hp1 | a0001 | c0001 | t0018 | g0210 | AFR | USA | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0059 | AFR | USA | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | USA | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | USA | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | LWK | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | LWK | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0165 | REF | REF | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0103 | REF | REF | E2F6_chr2_11439375_11471161 | E2F6 | chr2 | 11439375 | 11471161 |
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 |
---|
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:11444598
|
C | T | 1 | a0001c0001t0010 | 2 | HG01167.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1879G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 1879 | chr2 | 11444598 | |||||
chr2:11444710
|
T | C | 1 | a0001c0001t0010 | 2 | HG01167.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1767A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 1767 | chr2 | 11444710 | |||||
chr2:11444731
|
C | T | 1 | a0001c0001t0010 | 2 | HG01167.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1746G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 1746 | chr2 | 11444731 | |||||
chr2:11444742
|
C | A | 1 | a0001c0001t0014 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1735G>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 1735 | chr2 | 11444742 | |||||
chr2:11444842
|
C | T | 2 | a0001c0001t0007a0001c0001t0010 | 6 | HG01167.hp1 HG02615.hp2 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1635G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 1635 | chr2 | 11444842 | |||||
chr2:11444884
|
A | G | 1 | a0001c0001t0010 | 2 | HG01167.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1593T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 1593 | chr2 | 11444884 | |||||
chr2:11444963
|
T | C | 1 | a0001c0001t0011 | 2 | NA18989.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1514A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 1514 | chr2 | 11444963 | |||||
chr2:11445610
|
C | T | 1 | a0001c0001t0015 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*867G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 867 | chr2 | 11445610 | |||||
chr2:11445763
|
TC | T | 1 | a0001c0001t0005 | 9 | HG02015.hp2 NA18946.hp1 NA18946.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*713delG | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 713 | chr2 | 11445763 | |||||
chr2:11445817
|
T | C | 1 | a0001c0001t0004 | 12 | HG02004.hp1 HG02027.hp1 HG02129.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*660A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 660 | chr2 | 11445817 | |||||
chr2:11445909
|
G | A | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(10): Show | 176 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*568C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 568 | chr2 | 11445909 | |||||
chr2:11445910
|
T | C | 1 | a0001c0001t0006 | 5 | HG01070.hp1 HG01884.hp1 HG02109.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*567A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 567 | chr2 | 11445910 | |||||
chr2:11446093
|
A | G | 5 | a0001c0001t0002a0001c0001t0011a0001c0001t0012others(2): Show | 131 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*384T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 384 | chr2 | 11446093 | |||||
chr2:11446127
|
A | G | 1 | a0001c0001t0013 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*350T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 350 | chr2 | 11446127 | |||||
chr2:11446199
|
T | C | 1 | a0001c0001t0016 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*278A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 278 | chr2 | 11446199 | |||||
chr2:11446430
|
G | A | 1 | a0001c0001t0012 | 2 | HG03654.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*47C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 7/7 | 47 | chr2 | 11446430 | |||||
chr2:11465939
|
C | T | 1 | a0001c0001t0008 | 3 | HG02622.hp1 HG03130.hp2 HG06807.hp2 |
5_prime_UTR_variant | MODIFIER | c.-60G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/7 | 60 | chr2 | 11465939 | |||||
chr2:11465994
|
G | A | 1 | a0001c0001t0017 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-115C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/7 | 115 | chr2 | 11465994 | |||||
chr2:11466058
|
G | A | 1 | a0001c0001t0010 | 2 | HG01167.hp1 NA20805.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-179C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/7 | chr2 | 11466058 | ||||||
chr2:11466097
|
A | G | 1 | a0001c0001t0010 | 2 | HG01167.hp1 NA20805.hp2 |
5_prime_UTR_variant | MODIFIER | c.-218T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/7 | 218 | chr2 | 11466097 | |||||
chr2:11466106
|
A | G | 1 | a0001c0001t0009 | 2 | HG02451.hp2 HG02965.hp1 |
5_prime_UTR_variant | MODIFIER | c.-227T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/7 | 227 | chr2 | 11466106 | |||||
chr2:11466130
|
G | A | 1 | a0001c0001t0018 | 1 | HG06807.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-251C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/7 | chr2 | 11466130 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:11446553
|
C | A | 9 | a0001c0001t0003g0034a0001c0001t0003g0090a0001c0001t0003g0091others(6): Show | 10 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.800-30G>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11446553 | ||||||
chr2:11446567
|
C | G | 1 | a0001c0001t0002g0151 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.800-44G>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11446567 | ||||||
chr2:11446572
|
T | C | 4 | a0001c0001t0003g0086a0001c0001t0003g0087a0001c0001t0003g0088others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-49A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11446572 | ||||||
chr2:11446580
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.800-57A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11446580 | ||||||
chr2:11446678
|
G | A | 1 | a0001c0001t0002g0114 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.800-155C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11446678 | ||||||
chr2:11446755
|
A | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.800-232T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11446755 | ||||||
chr2:11446794
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.800-271G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11446794 | ||||||
chr2:11446809
|
A | C | 3 | a0001c0001t0007g0052a0001c0001t0007g0081a0001c0001t0007g0084 | 4 | HG02615.hp2 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.800-286T>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11446809 | ||||||
chr2:11446842
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.800-319A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11446842 | ||||||
chr2:11447005
|
TCGGTGGA others(16): Show |
T | 1 | a0001c0001t0012g0154 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.800-505_800-483del others(23): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11447005 | ||||||
chr2:11447030
|
G | C | 1 | a0001c0001t0012g0154 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.800-507C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11447030 | ||||||
chr2:11447031
|
T | G | 1 | a0001c0001t0012g0154 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.800-508A>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11447031 | ||||||
chr2:11447067
|
T | C | 5 | a0001c0001t0007g0052a0001c0001t0007g0081a0001c0001t0007g0084others(2): Show | 6 | HG01167.hp1 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.800-544A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11447067 | ||||||
chr2:11447105
|
T | G | 1 | a0001c0001t0002g0171 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.799+522A>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11447105 | ||||||
chr2:11447177
|
C | T | 1 | a0001c0001t0003g0088 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.799+450G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11447177 | ||||||
chr2:11447287
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799+340G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11447287 | ||||||
chr2:11447324
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0017g0209 | 5 | HG03669.hp2 HG03927.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.799+303A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11447324 | ||||||
chr2:11447427
|
A | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.799+200T>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11447427 | ||||||
chr2:11447505
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.799+122G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11447505 | ||||||
chr2:11447522
|
T | C | 1 | a0001c0001t0003g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.799+105A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11447522 | ||||||
chr2:11447567
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.799+60G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11447567 | ||||||
chr2:11447581
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.799+46A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 6/6 | chr2 | 11447581 | ||||||
chr2:11447827
|
T | C | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.652-53A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11447827 | ||||||
chr2:11447855
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.652-81C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11447855 | ||||||
chr2:11447929
|
A | G | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.652-155T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11447929 | ||||||
chr2:11448069
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.652-295G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448069 | ||||||
chr2:11448085
|
C | T | 4 | a0001c0001t0003g0121a0001c0001t0003g0127a0001c0001t0006g0010others(1): Show | 7 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.652-311G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448085 | ||||||
chr2:11448116
|
G | C | 1 | a0001c0001t0007g0052 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.652-342C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448116 | ||||||
chr2:11448122
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.652-348A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448122 | ||||||
chr2:11448219
|
G | A | 3 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0183 | 3 | HG02486.hp2 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.652-445C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448219 | ||||||
chr2:11448222
|
T | C | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 4 | HG01109.hp2 HG02258.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.652-448A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448222 | ||||||
chr2:11448313
|
C | T | 1 | a0001c0001t0003g0088 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.652-539G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448313 | ||||||
chr2:11448352
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.652-578A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448352 | ||||||
chr2:11448365
|
TAAGGA | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0080a0001c0001t0001g0083others(2): Show | 8 | HG01261.hp2 HG02622.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.652-596_652-592del others(5): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448365 | ||||||
chr2:11448402
|
G | T | 21 | a0001c0001t0003g0008a0001c0001t0003g0034a0001c0001t0003g0079others(18): Show | 26 | HG00639.hp1 HG01175.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.652-628C>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448402 | ||||||
chr2:11448408
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.652-634A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448408 | ||||||
chr2:11448423
|
A | G | 1 | a0001c0001t0002g0165 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.652-649T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448423 | ||||||
chr2:11448427
|
T | G | 1 | a0001c0001t0003g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.652-653A>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448427 | ||||||
chr2:11448448
|
C | A | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.652-674G>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448448 | ||||||
chr2:11448509
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.652-735C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448509 | ||||||
chr2:11448553
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.652-779C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448553 | ||||||
chr2:11448572
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.652-798G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448572 | ||||||
chr2:11448637
|
C | G | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.652-863G>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448637 | ||||||
chr2:11448660
|
A | T | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.652-886T>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448660 | ||||||
chr2:11448736
|
A | C | 1 | a0001c0001t0001g0130 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.652-962T>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448736 | ||||||
chr2:11448801
|
T | C | 1 | a0001c0001t0003g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.652-1027A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11448801 | ||||||
chr2:11449061
|
A | C | 1 | a0001c0001t0004g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.651+951T>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11449061 | ||||||
chr2:11449148
|
G | A | 75 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0011others(72): Show | 138 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.651+864C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11449148 | ||||||
chr2:11449228
|
A | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0131 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.651+784T>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11449228 | ||||||
chr2:11449236
|
C | A | 102 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0011others(99): Show | 172 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.651+776G>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11449236 | ||||||
chr2:11449285
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.651+727C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11449285 | ||||||
chr2:11449303
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(205): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.651+709T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11449303 | ||||||
chr2:11449322
|
C | T | 1 | a0001c0001t0001g0030 | 2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.651+690G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11449322 | ||||||
chr2:11449545
|
T | C | 1 | a0001c0001t0002g0061 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.651+467A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11449545 | ||||||
chr2:11449630
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.651+382A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11449630 | ||||||
chr2:11449729
|
G | C | 1 | a0001c0001t0003g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.651+283C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11449729 | ||||||
chr2:11449880
|
G | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.651+132C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 5/6 | chr2 | 11449880 | ||||||
chr2:11450276
|
A | T | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.537-150T>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11450276 | ||||||
chr2:11450285
|
A | C | 1 | a0001c0001t0001g0163 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.537-159T>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11450285 | ||||||
chr2:11450373
|
C | G | 1 | a0001c0001t0003g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.537-247G>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11450373 | ||||||
chr2:11450420
|
A | G | 2 | a0001c0001t0007g0081a0001c0001t0007g0084 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.537-294T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11450420 | ||||||
chr2:11450453
|
A | G | 150 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0016others(147): Show | 242 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(239): Show |
intron_variant | MODIFIER | c.537-327T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11450453 | ||||||
chr2:11450511
|
A | G | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.537-385T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11450511 | ||||||
chr2:11450624
|
C | T | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.537-498G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11450624 | ||||||
chr2:11450665
|
C | A | 1 | a0001c0001t0002g0172 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.537-539G>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11450665 | ||||||
chr2:11450689
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.537-563G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11450689 | ||||||
chr2:11450796
|
C | T | 1 | a0001c0001t0003g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.537-670G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11450796 | ||||||
chr2:11450820
|
TAG | T | 3 | a0001c0001t0007g0052a0001c0001t0007g0081a0001c0001t0007g0084 | 4 | HG02615.hp2 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.537-696_537-695del others(2): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11450820 | ||||||
chr2:11450986
|
G | A | 2 | a0001c0001t0007g0081a0001c0001t0007g0084 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.536+665C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11450986 | ||||||
chr2:11451012
|
C | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0126 | 4 | HG00639.hp2 HG02717.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.536+639G>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11451012 | ||||||
chr2:11451056
|
G | C | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.536+595C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11451056 | ||||||
chr2:11451236
|
C | T | 2 | a0001c0001t0002g0150a0001c0001t0002g0162 | 2 | HG02056.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.536+415G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11451236 | ||||||
chr2:11451330
|
C | A | 1 | a0001c0001t0007g0052 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.536+321G>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11451330 | ||||||
chr2:11451343
|
CCTAA | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0030others(24): Show | 38 | HG00438.hp1 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.536+304_536+307del others(4): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11451343 | ||||||
chr2:11451348
|
CT | C | 94 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0011others(91): Show | 162 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.536+302delA | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11451348 | ||||||
chr2:11451373
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.536+278C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11451373 | ||||||
chr2:11451517
|
T | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0080a0001c0001t0001g0083others(2): Show | 8 | HG01261.hp2 HG02622.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.536+134A>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 4/6 | chr2 | 11451517 | ||||||
chr2:11452022
|
C | A | 4 | a0001c0001t0003g0121a0001c0001t0003g0127a0001c0001t0006g0010others(1): Show | 7 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.381-216G>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11452022 | ||||||
chr2:11452152
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.381-346G>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11452152 | ||||||
chr2:11452168
|
G | T | 73 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0011others(70): Show | 136 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.381-362C>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11452168 | ||||||
chr2:11452433
|
G | A | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.381-627C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11452433 | ||||||
chr2:11452465
|
G | A | 4 | a0001c0001t0003g0121a0001c0001t0003g0127a0001c0001t0006g0010others(1): Show | 7 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.381-659C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11452465 | ||||||
chr2:11452553
|
G | A | 3 | a0001c0001t0002g0082a0001c0001t0002g0143a0001c0001t0002g0156 | 3 | HG02572.hp2 HG02735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.381-747C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11452553 | ||||||
chr2:11452779
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.380+803C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11452779 | ||||||
chr2:11452956
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.380+626A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11452956 | ||||||
chr2:11453134
|
G | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0029a0001c0001t0001g0051others(2): Show | 11 | HG00099.hp1 HG00741.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.380+448C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11453134 | ||||||
chr2:11453137
|
A | G | 1 | a0001c0001t0001g0037 | 2 | NA19002.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.380+445T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11453137 | ||||||
chr2:11453185
|
T | A | 1 | a0001c0001t0001g0033 | 2 | NA18965.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.380+397A>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11453185 | ||||||
chr2:11453366
|
C | T | 2 | a0001c0001t0007g0081a0001c0001t0007g0084 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.380+216G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11453366 | ||||||
chr2:11453370
|
A | G | 70 | a0001c0001t0001g0155a0001c0001t0002g0002a0001c0001t0002g0003others(67): Show | 132 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.380+212T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11453370 | ||||||
chr2:11453529
|
T | C | 1 | a0001c0001t0007g0052 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.380+53A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11453529 | ||||||
chr2:11453567
|
T | G | 1 | a0001c0001t0001g0078 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.380+15A>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 3/6 | chr2 | 11453567 | ||||||
chr2:11453818
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.164-20A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11453818 | ||||||
chr2:11453894
|
A | T | 1 | a0001c0001t0002g0169 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164-96T>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11453894 | ||||||
chr2:11454036
|
A | G | 1 | a0001c0001t0003g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.164-238T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11454036 | ||||||
chr2:11454049
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.164-251G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11454049 | ||||||
chr2:11454132
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.164-334A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11454132 | ||||||
chr2:11454290
|
G | A | 1 | a0001c0001t0003g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.164-492C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11454290 | ||||||
chr2:11454344
|
ATCTC | A | 3 | a0001c0001t0007g0052a0001c0001t0007g0081a0001c0001t0007g0084 | 4 | HG02615.hp2 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-550_164-547del others(4): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11454344 | ||||||
chr2:11454352
|
C | CT | 11 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0072others(8): Show | 13 | HG01167.hp1 HG01255.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.164-555dupA | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11454352 | ||||||
chr2:11454461
|
TCTC | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0066 | 5 | HG02109.hp1 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-666_164-664del others(3): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11454461 | ||||||
chr2:11454510
|
A | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0102a0001c0001t0005g0101 | 3 | NA18946.hp1 NA18953.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.164-712T>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11454510 | ||||||
chr2:11454613
|
T | G | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.164-815A>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11454613 | ||||||
chr2:11454629
|
A | G | 106 | a0001c0001t0001g0155a0001c0001t0002g0002a0001c0001t0002g0003others(103): Show | 177 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.164-831T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11454629 | ||||||
chr2:11454648
|
G | A | 1 | a0001c0001t0002g0061 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.164-850C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11454648 | ||||||
chr2:11454670
|
A | C | 1 | a0001c0001t0010g0055 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.164-872T>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11454670 | ||||||
chr2:11454911
|
T | C | 7 | a0001c0001t0003g0086a0001c0001t0003g0087a0001c0001t0003g0088others(4): Show | 10 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-1113A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11454911 | ||||||
chr2:11455128
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.164-1330T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11455128 | ||||||
chr2:11455137
|
G | A | 2 | a0001c0001t0007g0081a0001c0001t0007g0084 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.164-1339C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11455137 | ||||||
chr2:11455407
|
G | A | 2 | a0001c0001t0002g0157a0001c0001t0002g0173 | 2 | NA18968.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.164-1609C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11455407 | ||||||
chr2:11455493
|
T | C | 1 | a0001c0001t0002g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.163+1686A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11455493 | ||||||
chr2:11455512
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.163+1667C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11455512 | ||||||
chr2:11455522
|
C | T | 3 | a0001c0001t0001g0100a0001c0001t0010g0055a0001c0001t0010g0056 | 3 | HG01167.hp1 NA18940.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.163+1657G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11455522 | ||||||
chr2:11455635
|
T | C | 1 | a0001c0001t0008g0058 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.163+1544A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11455635 | ||||||
chr2:11455653
|
A | G | 2 | a0001c0001t0003g0176a0001c0001t0003g0194 | 2 | HG01175.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.163+1526T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11455653 | ||||||
chr2:11455654
|
T | C | 4 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0076others(1): Show | 4 | HG02145.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+1525A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11455654 | ||||||
chr2:11455660
|
T | C | 1 | a0001c0001t0006g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.163+1519A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11455660 | ||||||
chr2:11455841
|
C | G | 1 | a0001c0001t0002g0142 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.163+1338G>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11455841 | ||||||
chr2:11455936
|
G | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.163+1243C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11455936 | ||||||
chr2:11455946
|
G | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.163+1233C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11455946 | ||||||
chr2:11456012
|
G | C | 2 | a0001c0001t0003g0121a0001c0001t0003g0127 | 2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.163+1167C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11456012 | ||||||
chr2:11456085
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0197 | 3 | HG00099.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.163+1094G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11456085 | ||||||
chr2:11456149
|
T | C | 2 | a0001c0001t0007g0081a0001c0001t0007g0084 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.163+1030A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11456149 | ||||||
chr2:11456209
|
C | T | 1 | a0001c0001t0003g0088 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.163+970G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11456209 | ||||||
chr2:11456356
|
A | G | 3 | a0001c0001t0007g0052a0001c0001t0007g0081a0001c0001t0007g0084 | 4 | HG02615.hp2 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+823T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11456356 | ||||||
chr2:11456471
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.163+708T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11456471 | ||||||
chr2:11456600
|
T | A | 1 | a0001c0001t0003g0088 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.163+579A>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11456600 | ||||||
chr2:11456770
|
C | T | 1 | a0001c0001t0007g0052 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.163+409G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11456770 | ||||||
chr2:11456780
|
T | C | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.163+399A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11456780 | ||||||
chr2:11456946
|
C | G | 2 | a0001c0001t0003g0086a0001c0001t0003g0087 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.163+233G>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11456946 | ||||||
chr2:11457025
|
A | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.163+154T>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11457025 | ||||||
chr2:11457034
|
T | G | 2 | a0001c0001t0007g0081a0001c0001t0007g0084 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.163+145A>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11457034 | ||||||
chr2:11457053
|
A | T | 3 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0183 | 3 | HG02486.hp2 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.163+126T>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 2/6 | chr2 | 11457053 | ||||||
chr2:11457340
|
T | C | 1 | a0001c0001t0003g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.109-107A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11457340 | ||||||
chr2:11457389
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.109-156G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11457389 | ||||||
chr2:11457402
|
T | C | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.109-169A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11457402 | ||||||
chr2:11457687
|
G | A | 1 | a0001c0001t0007g0052 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.109-454C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11457687 | ||||||
chr2:11457782
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(204): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.109-549G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11457782 | ||||||
chr2:11458158
|
C | T | 21 | a0001c0001t0003g0008a0001c0001t0003g0034a0001c0001t0003g0090others(18): Show | 26 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.109-925G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11458158 | ||||||
chr2:11458239
|
A | T | 1 | a0001c0001t0001g0106 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.109-1006T>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11458239 | ||||||
chr2:11458244
|
C | G | 1 | a0001c0001t0003g0087 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.109-1011G>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11458244 | ||||||
chr2:11458415
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.109-1182A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11458415 | ||||||
chr2:11458429
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.109-1196A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11458429 | ||||||
chr2:11458503
|
A | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.109-1270T>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11458503 | ||||||
chr2:11458533
|
T | G | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.109-1300A>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11458533 | ||||||
chr2:11458611
|
T | C | 5 | a0001c0001t0002g0011a0001c0001t0002g0043a0001c0001t0002g0044others(2): Show | 10 | HG00609.hp2 NA18941.hp2 NA18944.hp2 others(7): Show |
intron_variant | MODIFIER | c.109-1378A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11458611 | ||||||
chr2:11458843
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.109-1610C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11458843 | ||||||
chr2:11458864
|
A | C | 163 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0016others(160): Show | 259 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.109-1631T>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11458864 | ||||||
chr2:11459140
|
C | T | 3 | a0001c0001t0003g0086a0001c0001t0003g0087a0001c0001t0003g0088 | 3 | HG02257.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.109-1907G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459140 | ||||||
chr2:11459150
|
C | T | 107 | a0001c0001t0001g0039a0001c0001t0001g0155a0001c0001t0002g0002others(104): Show | 179 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.109-1917G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459150 | ||||||
chr2:11459171
|
A | T | 1 | a0001c0001t0003g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.109-1938T>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459171 | ||||||
chr2:11459282
|
A | C | 1 | a0001c0001t0003g0194 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.109-2049T>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459282 | ||||||
chr2:11459370
|
T | C | 4 | a0001c0001t0003g0121a0001c0001t0003g0127a0001c0001t0006g0010others(1): Show | 7 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.109-2137A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459370 | ||||||
chr2:11459419
|
C | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.109-2186G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459419 | ||||||
chr2:11459606
|
G | A | 68 | a0001c0001t0001g0039a0001c0001t0001g0155a0001c0001t0002g0002others(65): Show | 129 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.109-2373C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459606 | ||||||
chr2:11459607
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.109-2374G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459607 | ||||||
chr2:11459662
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.109-2429A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459662 | ||||||
chr2:11459671
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.109-2438G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459671 | ||||||
chr2:11459679
|
C | G | 68 | a0001c0001t0001g0155a0001c0001t0002g0002a0001c0001t0002g0003others(65): Show | 128 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.109-2446G>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459679 | ||||||
chr2:11459818
|
G | T | 3 | a0001c0001t0003g0086a0001c0001t0003g0087a0001c0001t0003g0088 | 3 | HG02257.hp1 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.109-2585C>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459818 | ||||||
chr2:11459850
|
C | A | 1 | a0001c0001t0001g0097 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.109-2617G>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459850 | ||||||
chr2:11459866
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.109-2633C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459866 | ||||||
chr2:11459878
|
C | T | 4 | a0001c0001t0003g0121a0001c0001t0003g0127a0001c0001t0006g0010others(1): Show | 7 | HG01070.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.109-2645G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459878 | ||||||
chr2:11459883
|
CA | C | 75 | a0001c0001t0001g0155a0001c0001t0002g0002a0001c0001t0002g0003others(72): Show | 136 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.109-2651delT | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11459883 | ||||||
chr2:11460139
|
G | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.109-2906C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460139 | ||||||
chr2:11460314
|
C | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0016others(38): Show | 60 | HG00438.hp1 HG00609.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.109-3081G>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460314 | ||||||
chr2:11460317
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.109-3084T>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460317 | ||||||
chr2:11460325
|
AT | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(206): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.109-3093delA | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460325 | ||||||
chr2:11460350
|
A | G | 1 | a0001c0001t0008g0058 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.109-3117T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460350 | ||||||
chr2:11460436
|
T | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0187 | 5 | HG02451.hp1 HG02572.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-3203A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460436 | ||||||
chr2:11460479
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.109-3246A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460479 | ||||||
chr2:11460537
|
G | A | 3 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0183 | 3 | HG02486.hp2 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.109-3304C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460537 | ||||||
chr2:11460555
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.109-3322C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460555 | ||||||
chr2:11460673
|
A | G | 5 | a0001c0001t0001g0099a0001c0001t0001g0102a0001c0001t0001g0117others(2): Show | 5 | HG02074.hp1 NA18946.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.109-3440T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460673 | ||||||
chr2:11460674
|
T | C | 5 | a0001c0001t0002g0026a0001c0001t0002g0042a0001c0001t0002g0146others(2): Show | 8 | NA18948.hp1 NA18953.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.109-3441A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460674 | ||||||
chr2:11460812
|
T | C | 1 | a0001c0001t0003g0088 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.109-3579A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460812 | ||||||
chr2:11460883
|
G | C | 4 | a0001c0001t0003g0079a0001c0001t0007g0052a0001c0001t0007g0081others(1): Show | 5 | HG01884.hp2 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.109-3650C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460883 | ||||||
chr2:11460951
|
G | A | 3 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0183 | 3 | HG02486.hp2 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.109-3718C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460951 | ||||||
chr2:11460956
|
GGAGT | G | 21 | a0001c0001t0003g0008a0001c0001t0003g0034a0001c0001t0003g0090others(18): Show | 26 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.109-3727_109-3724d others(6): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11460956 | ||||||
chr2:11461047
|
G | C | 1 | a0001c0001t0003g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.109-3814C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11461047 | ||||||
chr2:11461078
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0130 | 4 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-3845C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11461078 | ||||||
chr2:11461113
|
C | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0098a0001c0001t0001g0130others(1): Show | 6 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-3880G>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11461113 | ||||||
chr2:11461162
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.109-3929G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11461162 | ||||||
chr2:11461351
|
A | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0016others(29): Show | 46 | HG00438.hp1 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.109-4118T>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11461351 | ||||||
chr2:11461382
|
A | G | 108 | a0001c0001t0001g0022a0001c0001t0001g0124a0001c0001t0001g0126others(105): Show | 179 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.109-4149T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11461382 | ||||||
chr2:11461438
|
A | G | 68 | a0001c0001t0001g0155a0001c0001t0002g0002a0001c0001t0002g0003others(65): Show | 128 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.109-4205T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11461438 | ||||||
chr2:11461702
|
T | G | 22 | a0001c0001t0003g0008a0001c0001t0003g0034a0001c0001t0003g0090others(19): Show | 27 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.108+4070A>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11461702 | ||||||
chr2:11461769
|
G | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.108+4003C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11461769 | ||||||
chr2:11461783
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.108+3989T>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11461783 | ||||||
chr2:11461917
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.108+3855G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11461917 | ||||||
chr2:11461922
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.108+3850T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11461922 | ||||||
chr2:11462162
|
G | A | 102 | a0001c0001t0001g0022a0001c0001t0001g0124a0001c0001t0001g0126others(99): Show | 172 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.108+3610C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462162 | ||||||
chr2:11462289
|
G | C | 1 | a0001c0001t0007g0052 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.108+3483C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462289 | ||||||
chr2:11462325
|
G | A | 1 | a0001c0001t0003g0181 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.108+3447C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462325 | ||||||
chr2:11462364
|
C | G | 1 | a0001c0001t0003g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.108+3408G>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462364 | ||||||
chr2:11462399
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.108+3373A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462399 | ||||||
chr2:11462407
|
T | C | 1 | a0001c0001t0002g0136 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.108+3365A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462407 | ||||||
chr2:11462496
|
G | T | 1 | a0001c0001t0003g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.108+3276C>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462496 | ||||||
chr2:11462531
|
G | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.108+3241C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462531 | ||||||
chr2:11462577
|
C | T | 1 | a0001c0001t0002g0149 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.108+3195G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462577 | ||||||
chr2:11462586
|
CTACTGGA others(4): Show |
C | 1 | a0001c0001t0002g0137 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.108+3175_108+3185d others(13): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462586 | ||||||
chr2:11462600
|
C | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.108+3172G>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462600 | ||||||
chr2:11462706
|
G | A | 21 | a0001c0001t0003g0008a0001c0001t0003g0034a0001c0001t0003g0090others(18): Show | 26 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.108+3066C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462706 | ||||||
chr2:11462761
|
G | A | 21 | a0001c0001t0003g0008a0001c0001t0003g0034a0001c0001t0003g0090others(18): Show | 26 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.108+3011C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462761 | ||||||
chr2:11462801
|
A | G | 1 | a0001c0001t0003g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.108+2971T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462801 | ||||||
chr2:11462916
|
G | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.108+2856C>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462916 | ||||||
chr2:11462928
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.108+2844C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462928 | ||||||
chr2:11462955
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0080a0001c0001t0001g0083others(2): Show | 8 | HG01261.hp2 HG02622.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.108+2817A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11462955 | ||||||
chr2:11463009
|
T | C | 1 | a0001c0001t0003g0088 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.108+2763A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463009 | ||||||
chr2:11463024
|
G | C | 1 | a0001c0001t0009g0054 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.108+2748C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463024 | ||||||
chr2:11463055
|
T | G | 1 | a0001c0001t0002g0190 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.108+2717A>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463055 | ||||||
chr2:11463213
|
A | G | 1 | a0001c0001t0004g0198 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.108+2559T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463213 | ||||||
chr2:11463333
|
G | A | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.108+2439C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463333 | ||||||
chr2:11463354
|
A | G | 3 | a0001c0001t0002g0148a0001c0001t0002g0160a0001c0001t0002g0202 | 3 | HG02040.hp1 HG03688.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.108+2418T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463354 | ||||||
chr2:11463361
|
A | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0100 | 4 | NA18940.hp2 NA18974.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+2411T>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463361 | ||||||
chr2:11463559
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.108+2213C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463559 | ||||||
chr2:11463689
|
C | T | 3 | a0001c0001t0003g0090a0001c0001t0003g0091a0001c0001t0003g0092 | 3 | HG02145.hp1 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.108+2083G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463689 | ||||||
chr2:11463849
|
T | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0131 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.108+1923A>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463849 | ||||||
chr2:11463945
|
C | T | 132 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0016others(129): Show | 211 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.108+1827G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463945 | ||||||
chr2:11463948
|
C | CG | 13 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0029others(10): Show | 23 | HG00099.hp1 HG00544.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.108+1823dupC | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463948 | ||||||
chr2:11463948
|
C | CGGGG | 16 | a0001c0001t0001g0032a0001c0001t0001g0065a0001c0001t0001g0083others(13): Show | 34 | HG00738.hp1 HG01081.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.108+1820_108+1823d others(6): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463948 | ||||||
chr2:11463948
|
C | CGGGGG | 43 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0047others(40): Show | 80 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.108+1819_108+1823d others(7): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463948 | ||||||
chr2:11463948
|
C | CGGGGGG | 24 | a0001c0001t0001g0009a0001c0001t0001g0089a0001c0001t0001g0184others(21): Show | 38 | HG00735.hp2 HG01192.hp2 HG01261.hp2 others(35): Show |
intron_variant | MODIFIER | c.108+1818_108+1823d others(8): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463948 | ||||||
chr2:11463948
|
C | CGGGGGGG others(3): Show |
8 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0064others(5): Show | 10 | HG01346.hp1 HG01361.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+1814_108+1823d others(12): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463948 | ||||||
chr2:11463948
|
C | CGGGGGGG others(4): Show |
4 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0075others(1): Show | 4 | HG01069.hp2 HG01099.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+1823_108+1824i others(13): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463948 | ||||||
chr2:11463948
|
C | CGGGGGGG others(5): Show |
1 | a0001c0001t0001g0066 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.108+1823_108+1824i others(14): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463948 | ||||||
chr2:11463948
|
C | CGGGGGGG others(6): Show |
1 | a0001c0001t0003g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.108+1823_108+1824i others(15): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463948 | ||||||
chr2:11463948
|
C | CGGGGGGG others(8): Show |
1 | a0001c0001t0001g0074 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.108+1823_108+1824i others(17): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11463948 | ||||||
chr2:11464034
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.108+1738G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464034 | ||||||
chr2:11464052
|
T | C | 2 | a0001c0001t0002g0169a0001c0001t0002g0174 | 2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.108+1720A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464052 | ||||||
chr2:11464132
|
G | A | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.108+1640C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464132 | ||||||
chr2:11464249
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.108+1523C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464249 | ||||||
chr2:11464277
|
G | A | 28 | a0001c0001t0003g0008a0001c0001t0003g0034a0001c0001t0003g0086others(25): Show | 36 | HG00639.hp1 HG01070.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.108+1495C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464277 | ||||||
chr2:11464334
|
GA | G | 5 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0194others(2): Show | 5 | HG00639.hp1 HG01175.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.108+1437delT | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464334 | ||||||
chr2:11464467
|
A | C | 14 | a0001c0001t0003g0008a0001c0001t0003g0090a0001c0001t0003g0091others(11): Show | 18 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.108+1305T>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464467 | ||||||
chr2:11464510
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.108+1262A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464510 | ||||||
chr2:11464517
|
C | CA | 45 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0048others(42): Show | 64 | HG00438.hp2 HG00639.hp1 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.108+1254dupT | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464517 | ||||||
chr2:11464517
|
C | CAA | 6 | a0001c0001t0001g0119a0001c0001t0002g0175a0001c0001t0002g0193others(3): Show | 6 | HG02486.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.108+1253_108+1254d others(4): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464517 | ||||||
chr2:11464517
|
CA | C | 12 | a0001c0001t0001g0060a0001c0001t0001g0064a0001c0001t0001g0065others(9): Show | 15 | HG01069.hp2 HG01070.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.108+1254delT | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464517 | ||||||
chr2:11464517
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0063 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.108+1244_108+1254d others(13): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464517 | ||||||
chr2:11464553
|
A | G | 3 | a0001c0001t0001g0077a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | HG01496.hp1 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.108+1219T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464553 | ||||||
chr2:11464610
|
G | T | 1 | a0001c0001t0002g0135 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.108+1162C>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464610 | ||||||
chr2:11464671
|
T | C | 21 | a0001c0001t0003g0008a0001c0001t0003g0034a0001c0001t0003g0090others(18): Show | 26 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.108+1101A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464671 | ||||||
chr2:11464796
|
A | T | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.108+976T>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464796 | ||||||
chr2:11464854
|
A | G | 139 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0016others(136): Show | 226 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.108+918T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464854 | ||||||
chr2:11464910
|
C | T | 1 | a0001c0001t0002g0134 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.108+862G>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464910 | ||||||
chr2:11464983
|
A | G | 1 | a0001c0001t0002g0133 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.108+789T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464983 | ||||||
chr2:11464997
|
G | A | 1 | a0001c0001t0007g0052 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.108+775C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11464997 | ||||||
chr2:11465111
|
G | T | 1 | a0001c0001t0001g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.108+661C>A | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465111 | ||||||
chr2:11465170
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.108+602G>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465170 | ||||||
chr2:11465178
|
C | CA | 19 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0124others(16): Show | 25 | HG00609.hp2 HG00639.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.108+593dupT | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465178 | ||||||
chr2:11465178
|
C | CAA | 76 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(73): Show | 141 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.108+592_108+593dup others(2): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465178 | ||||||
chr2:11465178
|
C | CAAA | 8 | a0001c0001t0001g0192a0001c0001t0002g0014a0001c0001t0002g0189others(5): Show | 11 | HG01123.hp1 HG01175.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.108+591_108+593dup others(3): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465178 | ||||||
chr2:11465178
|
CA | C | 26 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0030others(23): Show | 37 | HG00438.hp1 HG00735.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.108+593delT | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465178 | ||||||
chr2:11465178
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0002g0061 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.108+581_108+593del others(13): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465178 | ||||||
chr2:11465179
|
A | AAAACTCA others(5): Show |
1 | a0001c0001t0001g0078 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.108+592_108+593ins others(12): Show |
E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465179 | ||||||
chr2:11465191
|
A | G | 1 | a0001c0001t0007g0052 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.108+581T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465191 | ||||||
chr2:11465198
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.108+574T>C | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465198 | ||||||
chr2:11465227
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.108+545C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465227 | ||||||
chr2:11465247
|
T | C | 1 | a0001c0001t0001g0049 | 2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.108+525A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465247 | ||||||
chr2:11465255
|
G | A | 17 | a0001c0001t0001g0015a0001c0001t0001g0029a0001c0001t0001g0051others(14): Show | 31 | HG00099.hp1 HG00544.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.108+517C>T | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465255 | ||||||
chr2:11465475
|
T | C | 1 | a0001c0001t0007g0052 | 2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.108+297A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465475 | ||||||
chr2:11465562
|
T | C | 1 | a0001c0001t0002g0208 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.108+210A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465562 | ||||||
chr2:11465572
|
T | C | 2 | a0001c0001t0010g0055a0001c0001t0010g0056 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.108+200A>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465572 | ||||||
chr2:11465694
|
G | C | 1 | a0001c0001t0017g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.108+78C>G | E2F6 | ENSG00000169016.17 | transcript | ENST00000381525.8 | protein_coding | 1/6 | chr2 | 11465694 |