geneid | 2146 |
---|---|
ensemblid | ENSG00000106462.12 |
hgncid | 3527 |
symbol | EZH2 |
name | enhancer of zeste 2 polycomb repressive complex 2 subunit |
refseq_nuc | NM_004456.5 |
refseq_prot | NP_004447.2 |
ensembl_nuc | ENST00000320356.7 |
ensembl_prot | ENSP00000320147.2 |
mane_status | MANE Select |
chr | chr7 |
start | 148807383 |
end | 148884291 |
strand | - |
ver | v1.2 |
region | chr7:148807383-148884291 |
region5000 | chr7:148802383-148889291 |
regionname0 | EZH2_chr7_148807383_148884291 |
regionname5000 | EZH2_chr7_148802383_148889291 |
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 | 751 | 345 | 92 | 65 | 146 | 12 | 28 | 120 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0002 | 0/0 | 751 | 34 | 0 | 5 | 26 | 2 | 1 | 14 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0003 | 0/0 | 751 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
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 | 2256 | 337 | 86 | 65 | 145 | 12 | 27 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
c0002 | 0/0 | 2256 | 33 | 0 | 4 | 26 | 2 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
c0003 | 0/0 | 2256 | 3 | 3 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
c0004 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
c0005 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
c0006 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
c0007 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
c0008 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
c0009 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
c0010 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
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 | 0/0 | 398 | 276 | 87 | 57 | 110 | 6 | 16 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
t0002 | 1/1 | 399 | 99 | 4 | 12 | 60 | 7 | 14 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
t0003 | 0/0 | 398 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
t0004 | 0/0 | 398 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
t0005 | 0/0 | 398 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
t0006 | 0/0 | 398 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
t0007 | 0/0 | 398 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
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 | 2 | 0 | 2 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0225 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
g0378 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
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 | 2256 | 337 | 86 | 65 | 145 | 12 | 27 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0003 | 0/0 | 2256 | 3 | 3 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0005 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0006 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0007 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0009 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0010 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0002c0002 | 0/0 | 2256 | 33 | 0 | 4 | 26 | 2 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0002c0004 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0003c0008 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2653 | 237 | 81 | 52 | 84 | 5 | 15 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0001t0002 | 1/1 | 2654 | 97 | 4 | 12 | 60 | 7 | 12 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0001t0004 | 0/0 | 2653 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0001t0005 | 0/0 | 2653 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0001t0006 | 0/0 | 2653 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0003t0001 | 0/0 | 2653 | 3 | 3 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0005t0001 | 0/0 | 2653 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0006t0002 | 0/0 | 2654 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0007t0001 | 0/0 | 2653 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0009t0001 | 0/0 | 2653 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0001c0010t0003 | 0/0 | 2653 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0002c0002t0001 | 0/0 | 2653 | 32 | 0 | 4 | 26 | 1 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0002c0002t0007 | 0/0 | 2653 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0002c0004t0001 | 0/0 | 2653 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
a0003c0008t0002 | 0/0 | 2654 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | copy fasta | chr7 | 148802383 | 148889291 |
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 | 2 | 0 | 2 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0225 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0005g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0001t0006g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0003t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0005t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0006t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0007t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0009t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0001c0010t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0002t0007g0378 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0002c0004t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
a0003c0008t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | GBR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0366 | EUR | GBR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0347 | EUR | FIN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | CHS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | CHS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | CHS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | CHS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | CHS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0333 | EAS | CHS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0345 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0344 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0328 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01257 | hp1 | a0002 | c0004 | t0001 | g0346 | AMR | CLM | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0365 | AMR | CLM | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0139 | AMR | CLM | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0342 | AMR | CLM | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | IBS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0282 | EUR | IBS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01516 | hp1 | a0002 | c0002 | t0007 | g0378 | EUR | IBS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0281 | EUR | IBS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0278 | EUR | IBS | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0369 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02055 | hp1 | a0001 | c0005 | t0001 | g0253 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0359 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0356 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0331 | EAS | KHV | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0326 | EAS | CDX | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CDX | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0355 | EAS | CDX | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0367 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0084 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02970 | hp1 | a0001 | c0007 | t0001 | g0376 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02976 | hp2 | a0001 | c0009 | t0001 | g0011 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0372 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0371 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0311 | AFR | ESN | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | GWD | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0377 | AFR | MSL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0288 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03710 | hp1 | a0001 | c0006 | t0002 | g0264 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0374 | SAS | PJL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0258 | SAS | BEB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0375 | SAS | BEB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0370 | SAS | BEB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03834 | hp2 | a0003 | c0008 | t0002 | g0200 | SAS | BEB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | BEB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0368 | SAS | BEB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | BEB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | CHB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0348 | EAS | CHB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0083 | AFR | YRI | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | YRI | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0358 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0350 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0349 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0362 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0360 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18977 | hp2 | a0001 | c0010 | t0003 | g0003 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0343 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0363 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0357 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0351 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0373 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ASW | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ASW | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0181 | EUR | TSI | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0275 | EUR | TSI | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0180 | EUR | TSI | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0215 | EUR | TSI | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0361 | AMR | CLM | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | USA | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | USA | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0341 | EAS | JPT | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | USA | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | USA | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0223 | REF | REF | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0225 | REF | REF | EZH2_chr7_148802383_148889291 | EZH2 | chr7 | 148802383 | 148889291 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:148816730
|
C | T | 1 | a0003 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.1459G>A | p.Ala487Thr | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 12/20 | 1594/2654 | 1459/2256 | 487/751 | chr7 | 148816730 | ||
chr7:148828812
|
C | G | 1 | a0002 | 34 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(31): Show |
missense_variant | MODERATE | c.553G>C | p.Asp185His | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/20 | 688/2654 | 553/2256 | 185/751 | chr7 | 148828812 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:148810334
|
A | G | 2 | a0001c0007a0001c0009 | 2 | HG02970.hp1 HG02976.hp2 |
splice_region_variant&synonymous_variant | LOW | c.2028T>C | p.Asn676Asn | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 17/20 | 2163/2654 | 2028/2256 | 676/751 | chr7 | 148810334 | ||
chr7:148815038
|
G | A | 1 | a0002c0004 | 1 | HG01257.hp1 | splice_region_variant&synonymous_variant | LOW | c.1548C>T | p.Asp516Asp | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 14/20 | 1683/2654 | 1548/2256 | 516/751 | chr7 | 148815038 | ||
chr7:148818100
|
A | G | 2 | a0001c0003a0001c0007 | 4 | HG02647.hp1 HG02970.hp1 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.1017T>C | p.Phe339Phe | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 10/20 | 1152/2654 | 1017/2256 | 339/751 | chr7 | 148818100 | ||
chr7:148819623
|
A | C | 1 | a0001c0006 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.972T>G | p.Pro324Pro | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 9/20 | 1107/2654 | 972/2256 | 324/751 | chr7 | 148819623 | ||
chr7:148826575
|
G | C | 1 | a0001c0010 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.786C>G | p.Pro262Pro | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/20 | 921/2654 | 786/2256 | 262/751 | chr7 | 148826575 | ||
chr7:148828807
|
A | G | 1 | a0001c0005 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.558T>C | p.Asp186Asp | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/20 | 693/2654 | 558/2256 | 186/751 | chr7 | 148828807 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:148807462
|
C | G | 1 | a0001c0001t0006 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*184G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 20/20 | 184 | chr7 | 148807462 | |||||
chr7:148807504
|
C | G | 1 | a0001c0001t0005 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*142G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 20/20 | 142 | chr7 | 148807504 | |||||
chr7:148807589
|
C | T | 1 | a0001c0001t0004 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*57G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 20/20 | 57 | chr7 | 148807589 | |||||
chr7:148807624
|
AG | A | 12 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(9): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*21delC | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 20/20 | 21 | chr7 | 148807624 | |||||
chr7:148884182
|
C | T | 1 | a0001c0010t0003 | 1 | NA18977.hp2 | 5_prime_UTR_variant | MODIFIER | c.-26G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/20 | 36884 | chr7 | 148884182 | |||||
chr7:148884276
|
G | A | 1 | a0002c0002t0007 | 1 | HG01516.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-120C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/20 | chr7 | 148884276 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:148807726
|
A | G | 4 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0003t0001g0083others(1): Show | 4 | HG02109.hp1 HG02647.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2196-20T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148807726 | ||||||
chr7:148807756
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2196-50C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148807756 | ||||||
chr7:148807762
|
A | AGACTT | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(255): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2196-61_2196-57dup others(5): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148807762 | ||||||
chr7:148807814
|
T | TA | 7 | a0001c0001t0001g0025a0001c0001t0002g0226a0001c0001t0002g0258others(4): Show | 7 | HG01175.hp2 HG02738.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.2196-109dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148807814 | ||||||
chr7:148807814
|
TA | T | 32 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(29): Show | 32 | HG00280.hp1 HG00423.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.2196-109delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148807814 | ||||||
chr7:148807814
|
TAA | T | 98 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032others(95): Show | 98 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.2196-110_2196-109d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148807814 | ||||||
chr7:148807814
|
TAAA | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(125): Show | 130 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.2196-111_2196-109d others(5): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148807814 | ||||||
chr7:148807814
|
TAAAAAAA | T | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2196-115_2196-109d others(9): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148807814 | ||||||
chr7:148807816
|
A | T | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2196-110T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148807816 | ||||||
chr7:148807836
|
A | C | 23 | a0001c0001t0001g0319a0002c0002t0001g0297a0002c0002t0001g0300others(20): Show | 23 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.2196-130T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148807836 | ||||||
chr7:148807894
|
G | C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2196-188C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148807894 | ||||||
chr7:148807950
|
T | C | 4 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0003t0001g0083others(1): Show | 4 | HG02109.hp1 HG02647.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2196-244A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148807950 | ||||||
chr7:148807951
|
G | T | 1 | a0001c0001t0002g0257 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2196-245C>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148807951 | ||||||
chr7:148808043
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2196-337G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808043 | ||||||
chr7:148808048
|
G | T | 1 | a0001c0001t0002g0293 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2196-342C>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808048 | ||||||
chr7:148808119
|
C | T | 1 | a0001c0001t0002g0198 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2196-413G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808119 | ||||||
chr7:148808154
|
G | A | 6 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG02717.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2196-448C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808154 | ||||||
chr7:148808161
|
G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(254): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.2196-455C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808161 | ||||||
chr7:148808163
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(254): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.2196-457T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808163 | ||||||
chr7:148808210
|
C | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(261): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.2196-504G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808210 | ||||||
chr7:148808267
|
A | T | 1 | a0001c0001t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2196-561T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808267 | ||||||
chr7:148808300
|
C | G | 1 | a0001c0001t0001g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2196-594G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808300 | ||||||
chr7:148808368
|
G | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(252): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.2196-662C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808368 | ||||||
chr7:148808390
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2195+681G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808390 | ||||||
chr7:148808406
|
T | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2195+665A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808406 | ||||||
chr7:148808652
|
C | T | 2 | a0001c0001t0002g0239a0001c0001t0002g0240 | 2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2195+419G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808652 | ||||||
chr7:148808696
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(242): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.2195+375A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808696 | ||||||
chr7:148808713
|
G | T | 1 | a0001c0001t0001g0066 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2195+358C>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808713 | ||||||
chr7:148808729
|
T | G | 1 | a0001c0001t0001g0113 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2195+342A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808729 | ||||||
chr7:148808737
|
T | C | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2195+334A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808737 | ||||||
chr7:148808768
|
G | A | 1 | a0002c0004t0001g0346 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2195+303C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808768 | ||||||
chr7:148808772
|
G | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(270): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.2195+299C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808772 | ||||||
chr7:148808893
|
A | G | 6 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG02717.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2195+178T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808893 | ||||||
chr7:148808919
|
A | G | 2 | a0001c0001t0001g0192a0001c0009t0001g0011 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2195+152T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808919 | ||||||
chr7:148808961
|
C | T | 2 | a0001c0003t0001g0083a0001c0003t0001g0084 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2195+110G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808961 | ||||||
chr7:148808972
|
A | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(261): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.2195+99T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 19/19 | chr7 | 148808972 | ||||||
chr7:148809271
|
T | G | 25 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(22): Show | 25 | HG00738.hp1 HG01123.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.2110+39A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 18/19 | chr7 | 148809271 | ||||||
chr7:148809304
|
A | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0114others(27): Show | 30 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(27): Show |
splice_region_variant&intron_variant | LOW | c.2110+6T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 18/19 | chr7 | 148809304 | ||||||
chr7:148809587
|
A | C | 1 | a0001c0009t0001g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2030-197T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 17/19 | chr7 | 148809587 | ||||||
chr7:148809617
|
C | G | 1 | a0001c0001t0001g0140 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2030-227G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 17/19 | chr7 | 148809617 | ||||||
chr7:148809658
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2030-268T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 17/19 | chr7 | 148809658 | ||||||
chr7:148809662
|
CA | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2030-273delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 17/19 | chr7 | 148809662 | ||||||
chr7:148809803
|
C | T | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2030-413G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 17/19 | chr7 | 148809803 | ||||||
chr7:148809854
|
A | G | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2030-464T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 17/19 | chr7 | 148809854 | ||||||
chr7:148810206
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2029+127G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 17/19 | chr7 | 148810206 | ||||||
chr7:148810229
|
T | C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2029+104A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 17/19 | chr7 | 148810229 | ||||||
chr7:148810266
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2029+67G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 17/19 | chr7 | 148810266 | ||||||
chr7:148810270
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2029+63G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 17/19 | chr7 | 148810270 | ||||||
chr7:148810442
|
C | A | 1 | a0001c0001t0001g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1948-28G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810442 | ||||||
chr7:148810442
|
C | CT | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0125others(3): Show | 8 | HG01106.hp2 HG01928.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1948-29dupA | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810442 | ||||||
chr7:148810568
|
G | A | 1 | a0001c0009t0001g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1948-154C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810568 | ||||||
chr7:148810725
|
T | A | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1948-311A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810725 | ||||||
chr7:148810756
|
C | T | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1948-342G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810756 | ||||||
chr7:148810764
|
C | T | 2 | a0001c0001t0002g0278a0001c0001t0002g0281 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1948-350G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810764 | ||||||
chr7:148810811
|
G | A | 28 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0299others(25): Show | 28 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1948-397C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810811 | ||||||
chr7:148810820
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1948-406G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810820 | ||||||
chr7:148810827
|
C | G | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1948-413G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810827 | ||||||
chr7:148810859
|
G | A | 1 | a0001c0001t0002g0232 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1948-445C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810859 | ||||||
chr7:148810896
|
C | CA | 94 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0025others(91): Show | 94 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1948-483dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810896 | ||||||
chr7:148810896
|
C | CAA | 17 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(14): Show | 17 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1948-484_1948-483d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810896 | ||||||
chr7:148810896
|
C | CAAAAAAA others(19): Show |
1 | a0001c0009t0001g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1948-508_1948-483d others(28): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810896 | ||||||
chr7:148810896
|
CA | C | 18 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0037others(15): Show | 18 | HG01978.hp2 HG02258.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1948-483delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810896 | ||||||
chr7:148810896
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0003t0001g0083a0001c0003t0001g0084 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1948-492_1948-483d others(12): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810896 | ||||||
chr7:148810922
|
A | AT | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0251 | 3 | HG02615.hp2 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1948-509dupA | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148810922 | ||||||
chr7:148811054
|
G | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1947+571C>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811054 | ||||||
chr7:148811076
|
G | C | 2 | a0001c0003t0001g0083a0001c0003t0001g0084 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1947+549C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811076 | ||||||
chr7:148811105
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1947+520T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811105 | ||||||
chr7:148811146
|
T | C | 1 | a0002c0004t0001g0346 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1947+479A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811146 | ||||||
chr7:148811174
|
C | T | 4 | a0001c0001t0001g0040a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG02055.hp2 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1947+451G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811174 | ||||||
chr7:148811190
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1947+435C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811190 | ||||||
chr7:148811215
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG02818.hp2 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1947+410G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811215 | ||||||
chr7:148811238
|
C | T | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1947+387G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811238 | ||||||
chr7:148811255
|
G | A | 28 | a0001c0001t0001g0046a0001c0001t0001g0143a0001c0001t0001g0144others(25): Show | 28 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.1947+370C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811255 | ||||||
chr7:148811389
|
A | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1947+236T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811389 | ||||||
chr7:148811402
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1947+223G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811402 | ||||||
chr7:148811403
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1947+222C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811403 | ||||||
chr7:148811441
|
G | A | 1 | a0001c0001t0002g0205 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1947+184C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811441 | ||||||
chr7:148811446
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1947+179G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811446 | ||||||
chr7:148811448
|
G | C | 1 | a0001c0001t0001g0080 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1947+177C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811448 | ||||||
chr7:148811513
|
T | G | 2 | a0001c0001t0002g0230a0001c0001t0002g0237 | 2 | NA18960.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1947+112A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 16/19 | chr7 | 148811513 | ||||||
chr7:148811741
|
A | G | 256 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(253): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1852-21T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148811741 | ||||||
chr7:148811873
|
G | A | 2 | a0001c0001t0002g0284a0001c0001t0002g0285 | 2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1852-153C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148811873 | ||||||
chr7:148811892
|
G | A | 1 | a0001c0010t0003g0003 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1852-172C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148811892 | ||||||
chr7:148812145
|
A | G | 5 | a0001c0001t0001g0192a0001c0003t0001g0083a0001c0003t0001g0084others(2): Show | 5 | HG02630.hp2 HG02647.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-425T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148812145 | ||||||
chr7:148812178
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0162 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1852-458G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148812178 | ||||||
chr7:148812198
|
G | A | 1 | a0002c0002t0001g0343 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1852-478C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148812198 | ||||||
chr7:148812364
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1852-644A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148812364 | ||||||
chr7:148812407
|
C | T | 5 | a0001c0001t0001g0088a0001c0001t0001g0104a0001c0001t0001g0124others(2): Show | 5 | HG00140.hp1 HG00639.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-687G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148812407 | ||||||
chr7:148812449
|
C | A | 1 | a0001c0001t0001g0289 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1852-729G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148812449 | ||||||
chr7:148812561
|
A | T | 1 | a0002c0002t0001g0297 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1852-841T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148812561 | ||||||
chr7:148812582
|
G | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0091 | 2 | HG01433.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1852-862C>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148812582 | ||||||
chr7:148812583
|
T | C | 2 | a0001c0001t0002g0263a0001c0001t0002g0265 | 2 | NA18943.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1852-863A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148812583 | ||||||
chr7:148812697
|
G | A | 1 | a0001c0001t0002g0223 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1852-977C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148812697 | ||||||
chr7:148812801
|
C | T | 13 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1852-1081G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148812801 | ||||||
chr7:148812821
|
T | C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1852-1101A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148812821 | ||||||
chr7:148813013
|
T | C | 2 | a0001c0001t0001g0147a0001c0001t0001g0155 | 2 | HG01943.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1851+946A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813013 | ||||||
chr7:148813052
|
T | TAC | 16 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0199others(13): Show | 16 | HG00621.hp1 HG00741.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1851+905_1851+906d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813052 | ||||||
chr7:148813052
|
T | TACACACA others(3): Show |
1 | a0001c0001t0001g0368 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1851+906_1851+907i others(12): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813052 | ||||||
chr7:148813052
|
TAC | T | 32 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(29): Show | 32 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1851+905_1851+906d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813052 | ||||||
chr7:148813053
|
A | ACACACAC others(1): Show |
7 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0093others(4): Show | 7 | HG02015.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1851+905_1851+906i others(10): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813053 | ||||||
chr7:148813055
|
A | ACACACG | 3 | a0001c0001t0001g0292a0002c0002t0001g0333a0002c0002t0001g0343 | 3 | HG00673.hp2 HG01891.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1851+903_1851+904i others(8): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813055 | ||||||
chr7:148813057
|
A | ACACG | 81 | a0001c0001t0001g0023a0001c0001t0001g0091a0001c0001t0001g0096others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1851+901_1851+902i others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813057 | ||||||
chr7:148813059
|
A | ACG | 13 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(10): Show | 13 | HG00408.hp2 HG01952.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1851+899_1851+900i others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813059 | ||||||
chr7:148813061
|
A | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(149): Show | 154 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.1851+898T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813061 | ||||||
chr7:148813063
|
A | G | 30 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(27): Show | 30 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1851+896T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813063 | ||||||
chr7:148813065
|
A | G | 2 | a0001c0001t0001g0374a0001c0001t0001g0375 | 2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1851+894T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813065 | ||||||
chr7:148813067
|
A | G | 1 | a0002c0002t0001g0348 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1851+892T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813067 | ||||||
chr7:148813080
|
C | A | 2 | a0001c0001t0001g0192a0001c0009t0001g0011 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1851+879G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813080 | ||||||
chr7:148813169
|
C | T | 2 | a0002c0002t0001g0333a0002c0002t0001g0343 | 2 | HG00673.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1851+790G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813169 | ||||||
chr7:148813207
|
G | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0095 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1851+752C>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813207 | ||||||
chr7:148813225
|
C | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1851+734G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813225 | ||||||
chr7:148813330
|
TA | T | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(259): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1851+628delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813330 | ||||||
chr7:148813609
|
T | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0130 | 2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1851+350A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813609 | ||||||
chr7:148813635
|
A | AACT | 14 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(11): Show | 14 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1851+321_1851+323d others(5): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813635 | ||||||
chr7:148813669
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1851+290A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813669 | ||||||
chr7:148813901
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1851+58T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 15/19 | chr7 | 148813901 | ||||||
chr7:148814171
|
C | T | 1 | a0001c0001t0002g0181 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1673-34G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 14/19 | chr7 | 148814171 | ||||||
chr7:148814416
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1673-279G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 14/19 | chr7 | 148814416 | ||||||
chr7:148814762
|
C | G | 1 | a0001c0001t0002g0194 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1672+152G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 14/19 | chr7 | 148814762 | ||||||
chr7:148814804
|
C | T | 1 | a0002c0002t0001g0326 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1672+110G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 14/19 | chr7 | 148814804 | ||||||
chr7:148815049
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0036 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1547-10C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 13/19 | chr7 | 148815049 | ||||||
chr7:148815077
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1547-38C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 13/19 | chr7 | 148815077 | ||||||
chr7:148815220
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1547-181G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 13/19 | chr7 | 148815220 | ||||||
chr7:148815348
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1546+158C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 13/19 | chr7 | 148815348 | ||||||
chr7:148815712
|
C | A | 1 | a0001c0001t0001g0255 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1506-166G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 12/19 | chr7 | 148815712 | ||||||
chr7:148815850
|
G | A | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1506-304C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 12/19 | chr7 | 148815850 | ||||||
chr7:148815901
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1506-355C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 12/19 | chr7 | 148815901 | ||||||
chr7:148815907
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1506-361G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 12/19 | chr7 | 148815907 | ||||||
chr7:148816033
|
G | C | 4 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0003t0001g0377others(1): Show | 4 | HG02647.hp1 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506-487C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 12/19 | chr7 | 148816033 | ||||||
chr7:148816137
|
G | C | 1 | a0001c0001t0001g0289 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1505+547C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 12/19 | chr7 | 148816137 | ||||||
chr7:148816178
|
T | C | 4 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0003t0001g0377others(1): Show | 4 | HG02647.hp1 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1505+506A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 12/19 | chr7 | 148816178 | ||||||
chr7:148816238
|
A | G | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1505+446T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 12/19 | chr7 | 148816238 | ||||||
chr7:148816369
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0054 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1505+315G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 12/19 | chr7 | 148816369 | ||||||
chr7:148816375
|
G | A | 93 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0091others(90): Show | 93 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1505+309C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 12/19 | chr7 | 148816375 | ||||||
chr7:148816415
|
C | G | 6 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(3): Show | 6 | HG01243.hp2 HG02809.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1505+269G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 12/19 | chr7 | 148816415 | ||||||
chr7:148816664
|
G | C | 4 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0003t0001g0377others(1): Show | 4 | HG02647.hp1 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1505+20C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 12/19 | chr7 | 148816664 | ||||||
chr7:148816894
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1411-116C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 11/19 | chr7 | 148816894 | ||||||
chr7:148817490
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1241-99T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 10/19 | chr7 | 148817490 | ||||||
chr7:148817526
|
G | A | 27 | a0001c0001t0001g0046a0001c0001t0001g0143a0001c0001t0001g0144others(24): Show | 27 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1241-135C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 10/19 | chr7 | 148817526 | ||||||
chr7:148817707
|
C | G | 4 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0003t0001g0377others(1): Show | 4 | HG02647.hp1 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+170G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 10/19 | chr7 | 148817707 | ||||||
chr7:148817829
|
C | T | 3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0003t0001g0377 | 3 | HG02647.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1240+48G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 10/19 | chr7 | 148817829 | ||||||
chr7:148817842
|
A | G | 4 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0003t0001g0377others(1): Show | 4 | HG02647.hp1 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240+35T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 10/19 | chr7 | 148817842 | ||||||
chr7:148818122
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02818.hp1 | splice_region_variant&intron_variant | LOW | c.1000-5C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 9/19 | chr7 | 148818122 | ||||||
chr7:148818164
|
T | C | 2 | a0001c0001t0001g0353a0001c0001t0001g0354 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1000-47A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 9/19 | chr7 | 148818164 | ||||||
chr7:148818195
|
A | T | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1000-78T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 9/19 | chr7 | 148818195 | ||||||
chr7:148818243
|
A | C | 1 | a0001c0001t0001g0049 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1000-126T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 9/19 | chr7 | 148818243 | ||||||
chr7:148818413
|
A | G | 1 | a0002c0002t0001g0329 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1000-296T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 9/19 | chr7 | 148818413 | ||||||
chr7:148818450
|
A | G | 1 | a0001c0001t0002g0283 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1000-333T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 9/19 | chr7 | 148818450 | ||||||
chr7:148818709
|
C | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0136 | 3 | HG02145.hp1 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1000-592G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 9/19 | chr7 | 148818709 | ||||||
chr7:148818760
|
T | C | 4 | a0001c0001t0002g0007a0001c0001t0002g0222a0001c0001t0002g0276others(1): Show | 4 | NA18962.hp1 NA18987.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000-643A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 9/19 | chr7 | 148818760 | ||||||
chr7:148819299
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.999+297G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 9/19 | chr7 | 148819299 | ||||||
chr7:148819920
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.908-233C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148819920 | ||||||
chr7:148819960
|
C | T | 7 | a0001c0001t0001g0307a0001c0001t0001g0314a0001c0001t0001g0318others(4): Show | 7 | NA18970.hp1 NA18973.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.908-273G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148819960 | ||||||
chr7:148820043
|
A | T | 1 | a0001c0003t0001g0083 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.908-356T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148820043 | ||||||
chr7:148820212
|
C | T | 68 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0299others(65): Show | 68 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.908-525G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148820212 | ||||||
chr7:148820364
|
T | G | 70 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.908-677A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148820364 | ||||||
chr7:148820525
|
C | G | 1 | a0001c0001t0001g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.908-838G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148820525 | ||||||
chr7:148820551
|
G | GA | 10 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(7): Show | 10 | HG01070.hp1 HG01070.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.908-865dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148820551 | ||||||
chr7:148820551
|
GA | G | 13 | a0001c0001t0001g0041a0001c0001t0001g0184a0001c0001t0001g0185others(10): Show | 13 | HG01978.hp1 HG02055.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.908-865delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148820551 | ||||||
chr7:148820605
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.908-918G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148820605 | ||||||
chr7:148820638
|
T | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.908-951A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148820638 | ||||||
chr7:148820954
|
T | TACCAGC | 9 | a0001c0001t0001g0057a0001c0001t0002g0208a0001c0001t0002g0262others(6): Show | 9 | HG00544.hp2 NA18943.hp1 NA18981.hp1 others(6): Show |
intron_variant | MODIFIER | c.908-1273_908-1268d others(8): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148820954 | ||||||
chr7:148820988
|
C | A | 3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0003t0001g0377 | 3 | HG02647.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.908-1301G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148820988 | ||||||
chr7:148821108
|
A | G | 1 | a0001c0001t0002g0010 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.908-1421T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148821108 | ||||||
chr7:148821116
|
T | C | 21 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0202others(18): Show | 21 | HG02040.hp1 HG02132.hp2 NA18949.hp1 others(18): Show |
intron_variant | MODIFIER | c.908-1429A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148821116 | ||||||
chr7:148821164
|
T | C | 3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0003t0001g0377 | 3 | HG02647.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.908-1477A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148821164 | ||||||
chr7:148821180
|
T | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0031 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.908-1493A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148821180 | ||||||
chr7:148821200
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0193 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.908-1513T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148821200 | ||||||
chr7:148821307
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026 | 3 | HG00738.hp1 HG01175.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.908-1620C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148821307 | ||||||
chr7:148821493
|
A | G | 1 | a0002c0002t0001g0331 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.908-1806T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148821493 | ||||||
chr7:148821581
|
T | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.908-1894A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148821581 | ||||||
chr7:148821854
|
A | C | 1 | a0001c0001t0001g0298 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.908-2167T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148821854 | ||||||
chr7:148821854
|
ATCTC | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.908-2171_908-2168d others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148821854 | ||||||
chr7:148821856
|
C | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02155.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.908-2169G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148821856 | ||||||
chr7:148821919
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(141): Show | 146 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.908-2232G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148821919 | ||||||
chr7:148822045
|
T | A | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.908-2358A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148822045 | ||||||
chr7:148822144
|
TAGAA | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026 | 3 | HG00738.hp1 HG01175.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.908-2461_908-2458d others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148822144 | ||||||
chr7:148822231
|
C | G | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.908-2544G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148822231 | ||||||
chr7:148822287
|
ATCACTTG others(3): Show |
A | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.908-2610_908-2601d others(12): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148822287 | ||||||
chr7:148822425
|
C | T | 3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0003t0001g0377 | 3 | HG02647.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.908-2738G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148822425 | ||||||
chr7:148822507
|
C | CA | 7 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0057others(4): Show | 7 | HG01106.hp1 HG02809.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.908-2821dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148822507 | ||||||
chr7:148822528
|
A | C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.908-2841T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148822528 | ||||||
chr7:148822540
|
G | C | 1 | a0001c0001t0001g0368 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.908-2853C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148822540 | ||||||
chr7:148822565
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.908-2878T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148822565 | ||||||
chr7:148822648
|
A | G | 2 | a0001c0003t0001g0083a0001c0003t0001g0084 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.908-2961T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148822648 | ||||||
chr7:148823289
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.907+3165A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148823289 | ||||||
chr7:148823472
|
C | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.907+2982G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148823472 | ||||||
chr7:148823633
|
T | C | 1 | a0001c0001t0001g0020 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.907+2821A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148823633 | ||||||
chr7:148823652
|
CT | C | 20 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0091others(17): Show | 20 | HG01081.hp1 HG01433.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.907+2801delA | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148823652 | ||||||
chr7:148823805
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0031 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.907+2649G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148823805 | ||||||
chr7:148823826
|
T | G | 79 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(76): Show | 79 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.907+2628A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148823826 | ||||||
chr7:148824005
|
C | T | 2 | a0001c0001t0001g0374a0001c0001t0001g0375 | 2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.907+2449G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148824005 | ||||||
chr7:148824161
|
A | AAAAATTA others(22): Show |
8 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(5): Show | 8 | HG00738.hp1 HG01175.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.907+2264_907+2292d others(31): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148824161 | ||||||
chr7:148824301
|
C | T | 1 | a0001c0001t0002g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.907+2153G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148824301 | ||||||
chr7:148824310
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.907+2144C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148824310 | ||||||
chr7:148824314
|
CA | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.907+2139delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148824314 | ||||||
chr7:148824324
|
A | C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.907+2130T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148824324 | ||||||
chr7:148824327
|
A | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0040a0001c0001t0001g0097others(7): Show | 10 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.907+2127T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148824327 | ||||||
chr7:148824342
|
C | A | 1 | a0001c0001t0002g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.907+2112G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148824342 | ||||||
chr7:148824392
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.907+2062C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148824392 | ||||||
chr7:148824583
|
A | C | 1 | a0001c0009t0001g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.907+1871T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148824583 | ||||||
chr7:148824733
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.907+1721C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148824733 | ||||||
chr7:148824741
|
C | T | 1 | a0001c0001t0001g0305 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.907+1713G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148824741 | ||||||
chr7:148825012
|
T | G | 1 | a0002c0002t0001g0329 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.907+1442A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825012 | ||||||
chr7:148825032
|
G | T | 1 | a0001c0001t0001g0025 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.907+1422C>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825032 | ||||||
chr7:148825158
|
T | C | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.907+1296A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825158 | ||||||
chr7:148825177
|
C | A | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(276): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.907+1277G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825177 | ||||||
chr7:148825225
|
T | G | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.907+1229A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825225 | ||||||
chr7:148825274
|
T | G | 3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0007t0001g0376 | 3 | HG02647.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.907+1180A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825274 | ||||||
chr7:148825469
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.907+985G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825469 | ||||||
chr7:148825546
|
G | T | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.907+908C>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825546 | ||||||
chr7:148825589
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0098 | 2 | HG00621.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.907+865G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825589 | ||||||
chr7:148825669
|
T | A | 1 | a0002c0002t0001g0348 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.907+785A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825669 | ||||||
chr7:148825734
|
G | A | 6 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG02717.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.907+720C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825734 | ||||||
chr7:148825801
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.907+653T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825801 | ||||||
chr7:148825807
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.907+647A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825807 | ||||||
chr7:148825809
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.907+645G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825809 | ||||||
chr7:148825838
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.907+616A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825838 | ||||||
chr7:148825962
|
G | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.907+492C>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825962 | ||||||
chr7:148825972
|
C | T | 2 | a0001c0001t0001g0374a0001c0001t0001g0375 | 2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.907+482G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825972 | ||||||
chr7:148825997
|
T | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | NA18941.hp1 NA18953.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.907+457A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148825997 | ||||||
chr7:148826023
|
G | A | 1 | a0002c0002t0001g0348 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.907+431C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148826023 | ||||||
chr7:148826082
|
A | C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.907+372T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148826082 | ||||||
chr7:148826204
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0136 | 3 | HG02145.hp1 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.907+250C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148826204 | ||||||
chr7:148826327
|
A | G | 2 | a0001c0001t0001g0353a0001c0001t0001g0354 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.907+127T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148826327 | ||||||
chr7:148826370
|
A | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.907+84T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 8/19 | chr7 | 148826370 | ||||||
chr7:148826865
|
C | G | 1 | a0002c0002t0001g0348 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.729-233G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 7/19 | chr7 | 148826865 | ||||||
chr7:148827124
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.728+40G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 7/19 | chr7 | 148827124 | ||||||
chr7:148827145
|
C | G | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.728+19G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 7/19 | chr7 | 148827145 | ||||||
chr7:148827384
|
A | G | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-118T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148827384 | ||||||
chr7:148827543
|
T | G | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.626-277A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148827543 | ||||||
chr7:148827550
|
A | G | 1 | a0001c0001t0001g0144 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.626-284T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148827550 | ||||||
chr7:148827596
|
G | C | 1 | a0001c0001t0001g0325 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.626-330C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148827596 | ||||||
chr7:148827660
|
C | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(297): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.626-394G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148827660 | ||||||
chr7:148827862
|
A | C | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.626-596T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148827862 | ||||||
chr7:148827924
|
T | C | 5 | a0001c0001t0001g0339a0001c0001t0001g0352a0001c0001t0001g0353others(2): Show | 5 | HG01123.hp1 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.626-658A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148827924 | ||||||
chr7:148827933
|
C | T | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.626-667G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148827933 | ||||||
chr7:148827989
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.626-723C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148827989 | ||||||
chr7:148828024
|
A | G | 4 | a0002c0002t0001g0297a0002c0002t0001g0300a0002c0002t0001g0301others(1): Show | 4 | HG00408.hp2 HG00544.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.625+716T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148828024 | ||||||
chr7:148828057
|
G | A | 4 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0003t0001g0377others(1): Show | 4 | HG02647.hp1 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.625+683C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148828057 | ||||||
chr7:148828104
|
C | T | 1 | a0001c0001t0001g0340 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.625+636G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148828104 | ||||||
chr7:148828112
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02809.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.625+628G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148828112 | ||||||
chr7:148828139
|
A | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.625+601T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148828139 | ||||||
chr7:148828290
|
A | G | 1 | a0001c0001t0001g0061 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.625+450T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148828290 | ||||||
chr7:148828373
|
G | A | 2 | a0001c0003t0001g0083a0001c0003t0001g0084 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.625+367C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148828373 | ||||||
chr7:148828500
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.625+240C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148828500 | ||||||
chr7:148828509
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.625+231A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148828509 | ||||||
chr7:148828715
|
A | G | 1 | a0001c0001t0001g0364 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.625+25T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 6/19 | chr7 | 148828715 | ||||||
chr7:148828887
|
C | T | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02615.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.485-7G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 5/19 | chr7 | 148828887 | ||||||
chr7:148829000
|
T | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.485-120A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 5/19 | chr7 | 148829000 | ||||||
chr7:148829346
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.484+382G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 5/19 | chr7 | 148829346 | ||||||
chr7:148829352
|
T | G | 1 | a0001c0001t0001g0027 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.484+376A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 5/19 | chr7 | 148829352 | ||||||
chr7:148829381
|
T | C | 20 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(17): Show | 20 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.484+347A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 5/19 | chr7 | 148829381 | ||||||
chr7:148829632
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.484+96T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 5/19 | chr7 | 148829632 | ||||||
chr7:148829640
|
A | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.484+88T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 5/19 | chr7 | 148829640 | ||||||
chr7:148829685
|
A | G | 3 | a0001c0001t0002g0266a0001c0001t0002g0270a0001c0001t0002g0271 | 3 | NA18993.hp1 NA18999.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.484+43T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 5/19 | chr7 | 148829685 | ||||||
chr7:148829974
|
CAG | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0091a0001c0001t0001g0159others(3): Show | 6 | HG01433.hp1 HG01978.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-128_364-127del others(2): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148829974 | ||||||
chr7:148830030
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.364-182T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148830030 | ||||||
chr7:148830284
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.364-436A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148830284 | ||||||
chr7:148830305
|
A | G | 374 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(371): Show | 376 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.364-457T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148830305 | ||||||
chr7:148830384
|
G | A | 20 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(17): Show | 20 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.364-536C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148830384 | ||||||
chr7:148830442
|
C | T | 5 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(2): Show | 5 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-594G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148830442 | ||||||
chr7:148830528
|
T | A | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-680A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148830528 | ||||||
chr7:148830550
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.364-702T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148830550 | ||||||
chr7:148830587
|
T | G | 1 | a0001c0001t0001g0018 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.364-739A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148830587 | ||||||
chr7:148830750
|
A | G | 13 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(10): Show | 13 | HG01243.hp2 HG02280.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.364-902T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148830750 | ||||||
chr7:148830754
|
T | G | 79 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(76): Show | 79 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.364-906A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148830754 | ||||||
chr7:148830883
|
G | A | 6 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(3): Show | 6 | HG00639.hp2 HG00738.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1035C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148830883 | ||||||
chr7:148830936
|
GAA | G | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1090_364-1089d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148830936 | ||||||
chr7:148830966
|
A | G | 10 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(7): Show | 10 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-1118T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148830966 | ||||||
chr7:148831046
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.364-1198G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148831046 | ||||||
chr7:148831174
|
GGAC | G | 6 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(3): Show | 6 | HG01243.hp2 HG02809.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1329_364-1327d others(5): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148831174 | ||||||
chr7:148831273
|
T | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.363+1361A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148831273 | ||||||
chr7:148831286
|
T | A | 1 | a0001c0001t0002g0220 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.363+1348A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148831286 | ||||||
chr7:148831297
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.363+1337G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148831297 | ||||||
chr7:148831367
|
ATTTC | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.363+1263_363+1266d others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148831367 | ||||||
chr7:148831427
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.363+1207A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148831427 | ||||||
chr7:148831452
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+1182C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148831452 | ||||||
chr7:148831778
|
A | G | 73 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.363+856T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148831778 | ||||||
chr7:148831872
|
T | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+762A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148831872 | ||||||
chr7:148831897
|
C | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.363+737G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148831897 | ||||||
chr7:148832009
|
A | G | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.363+625T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148832009 | ||||||
chr7:148832066
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.363+568A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148832066 | ||||||
chr7:148832187
|
C | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.363+447G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148832187 | ||||||
chr7:148832224
|
T | C | 1 | a0001c0001t0002g0283 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.363+410A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148832224 | ||||||
chr7:148832513
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.363+121A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148832513 | ||||||
chr7:148832515
|
A | C | 1 | a0001c0001t0001g0369 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.363+119T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148832515 | ||||||
chr7:148832591
|
A | G | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.363+43T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 4/19 | chr7 | 148832591 | ||||||
chr7:148832830
|
C | T | 8 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(5): Show | 8 | HG00738.hp1 HG01175.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.247-80G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148832830 | ||||||
chr7:148833120
|
T | C | 15 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(12): Show | 15 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.247-370A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833120 | ||||||
chr7:148833131
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.247-381G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833131 | ||||||
chr7:148833173
|
C | G | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.247-423G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833173 | ||||||
chr7:148833181
|
G | A | 1 | a0002c0002t0001g0327 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.247-431C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833181 | ||||||
chr7:148833187
|
G | A | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.247-437C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833187 | ||||||
chr7:148833196
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.247-446G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833196 | ||||||
chr7:148833197
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.247-447C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833197 | ||||||
chr7:148833202
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(142): Show | 147 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.247-452A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833202 | ||||||
chr7:148833229
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.247-479G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833229 | ||||||
chr7:148833243
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.247-493C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833243 | ||||||
chr7:148833253
|
T | A | 53 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0044others(50): Show | 53 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.247-503A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833253 | ||||||
chr7:148833274
|
C | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG00741.hp2 HG01978.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-524G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833274 | ||||||
chr7:148833286
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.247-536C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833286 | ||||||
chr7:148833291
|
T | C | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-541A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833291 | ||||||
chr7:148833314
|
A | G | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-564T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833314 | ||||||
chr7:148833337
|
G | A | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.247-587C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833337 | ||||||
chr7:148833382
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.247-632C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833382 | ||||||
chr7:148833406
|
G | A | 34 | a0002c0002t0001g0297a0002c0002t0001g0300a0002c0002t0001g0301others(31): Show | 34 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.247-656C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833406 | ||||||
chr7:148833408
|
G | C | 1 | a0001c0001t0001g0114 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.247-658C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833408 | ||||||
chr7:148833412
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0125others(5): Show | 10 | HG01106.hp1 HG01106.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.247-662C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833412 | ||||||
chr7:148833456
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0001g0088a0001c0001t0001g0104a0001c0001t0001g0124others(2): Show | 5 | HG00140.hp1 HG00639.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-716_247-707del others(10): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833456 | ||||||
chr7:148833461
|
AAAAAAAA others(3): Show |
A | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 240 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.247-721_247-712del others(10): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833461 | ||||||
chr7:148833466
|
A | T | 23 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(20): Show | 23 | HG02055.hp1 HG02145.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.247-716T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833466 | ||||||
chr7:148833626
|
T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.247-876A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833626 | ||||||
chr7:148833701
|
C | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-951G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833701 | ||||||
chr7:148833834
|
G | A | 2 | a0001c0003t0001g0083a0001c0003t0001g0084 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.247-1084C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833834 | ||||||
chr7:148833848
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0158 | 3 | HG01081.hp2 HG01109.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.247-1098G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833848 | ||||||
chr7:148833922
|
T | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.247-1172A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833922 | ||||||
chr7:148833979
|
T | C | 2 | a0001c0003t0001g0083a0001c0003t0001g0084 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.247-1229A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148833979 | ||||||
chr7:148834042
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.247-1292A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834042 | ||||||
chr7:148834054
|
T | C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.247-1304A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834054 | ||||||
chr7:148834065
|
T | G | 1 | a0001c0001t0001g0320 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.247-1315A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834065 | ||||||
chr7:148834147
|
A | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG02818.hp2 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.247-1397T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834147 | ||||||
chr7:148834160
|
T | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-1410A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834160 | ||||||
chr7:148834337
|
T | TTATA | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-1591_247-1588d others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834337 | ||||||
chr7:148834337
|
T | TTATATA | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(1): Show | 4 | HG02257.hp2 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-1593_247-1588d others(8): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834337 | ||||||
chr7:148834337
|
T | TTATATAT others(1): Show |
3 | a0001c0001t0001g0016a0001c0003t0001g0083a0001c0003t0001g0084 | 3 | HG02647.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.247-1595_247-1588d others(10): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834337 | ||||||
chr7:148834337
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.247-1599_247-1588d others(14): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834337 | ||||||
chr7:148834337
|
T | TTATATAT others(7): Show |
1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.247-1601_247-1588d others(16): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834337 | ||||||
chr7:148834350
|
TATAC | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0099a0001c0001t0005g0139 | 3 | HG01123.hp2 HG01261.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.247-1604_247-1601d others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834350 | ||||||
chr7:148834350
|
TATACACA others(1): Show |
T | 3 | a0001c0001t0001g0039a0001c0001t0001g0190a0001c0001t0001g0193 | 3 | HG01884.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.247-1608_247-1601d others(10): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834350 | ||||||
chr7:148834350
|
TATACACA others(3): Show |
T | 1 | a0001c0001t0001g0113 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.247-1610_247-1601d others(12): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834350 | ||||||
chr7:148834352
|
T | C | 1 | a0001c0001t0002g0189 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.247-1602A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834352 | ||||||
chr7:148834352
|
T | TAC | 6 | a0001c0001t0002g0177a0001c0001t0002g0178a0001c0001t0002g0194others(3): Show | 6 | HG01099.hp2 HG01361.hp2 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.247-1604_247-1603d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834352 | ||||||
chr7:148834352
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0192 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.247-1603_247-1602i others(18): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834352 | ||||||
chr7:148834352
|
T | TATATATA others(9): Show |
1 | a0001c0009t0001g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.247-1603_247-1602i others(18): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834352 | ||||||
chr7:148834352
|
TAC | T | 42 | a0001c0001t0001g0126a0001c0001t0001g0150a0001c0001t0001g0155others(39): Show | 42 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.247-1604_247-1603d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834352 | ||||||
chr7:148834352
|
TACAC | T | 76 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0024others(73): Show | 76 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.247-1606_247-1603d others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834352 | ||||||
chr7:148834352
|
TACACAC | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(42): Show | 47 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.247-1608_247-1603d others(8): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834352 | ||||||
chr7:148834352
|
TACACACA others(1): Show |
T | 77 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(74): Show | 77 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.247-1610_247-1603d others(10): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834352 | ||||||
chr7:148834352
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0319 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.247-1612_247-1603d others(12): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834352 | ||||||
chr7:148834354
|
C | T | 48 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(45): Show | 48 | HG00280.hp2 HG00544.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.247-1604G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834354 | ||||||
chr7:148834356
|
C | T | 65 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(62): Show | 65 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.247-1606G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834356 | ||||||
chr7:148834358
|
C | T | 128 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(125): Show | 128 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.247-1608G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834358 | ||||||
chr7:148834360
|
C | CATATATA others(19): Show |
1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.247-1611_247-1610i others(28): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834360 | ||||||
chr7:148834360
|
C | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(77): Show | 82 | HG00140.hp1 HG00639.hp1 HG01070.hp2 others(79): Show |
intron_variant | MODIFIER | c.247-1610G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834360 | ||||||
chr7:148834362
|
C | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(7): Show | 10 | HG01433.hp2 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.247-1612G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834362 | ||||||
chr7:148834364
|
C | T | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG00423.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-1614G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834364 | ||||||
chr7:148834366
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG00423.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-1616G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834366 | ||||||
chr7:148834368
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-1618G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834368 | ||||||
chr7:148834378
|
CACACAT | C | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-1634_247-1629d others(8): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834378 | ||||||
chr7:148834382
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.247-1632G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834382 | ||||||
chr7:148834395
|
T | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.247-1645A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834395 | ||||||
chr7:148834413
|
T | G | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.247-1663A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834413 | ||||||
chr7:148834559
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.247-1809G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834559 | ||||||
chr7:148834590
|
G | A | 1 | a0002c0002t0001g0301 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.247-1840C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834590 | ||||||
chr7:148834671
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.247-1921A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834671 | ||||||
chr7:148834787
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.247-2037G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834787 | ||||||
chr7:148834896
|
A | G | 5 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0222others(2): Show | 5 | NA18959.hp1 NA18962.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-2146T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148834896 | ||||||
chr7:148835217
|
C | T | 2 | a0001c0001t0001g0353a0001c0001t0001g0354 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.247-2467G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148835217 | ||||||
chr7:148835267
|
C | T | 1 | a0002c0002t0001g0301 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.247-2517G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148835267 | ||||||
chr7:148835303
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.247-2553C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148835303 | ||||||
chr7:148835308
|
A | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0135 | 3 | HG02965.hp2 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.247-2558T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148835308 | ||||||
chr7:148835416
|
C | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0031 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.247-2666G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148835416 | ||||||
chr7:148835423
|
C | CA | 16 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0048others(13): Show | 16 | HG00609.hp1 HG01106.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.247-2674dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148835423 | ||||||
chr7:148835591
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026 | 3 | HG00738.hp1 HG01175.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.247-2841G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148835591 | ||||||
chr7:148835618
|
C | G | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(1): Show | 4 | HG02615.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-2868G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148835618 | ||||||
chr7:148835863
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0031 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.247-3113T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148835863 | ||||||
chr7:148836292
|
C | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(276): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.247-3542G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148836292 | ||||||
chr7:148836409
|
C | T | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(1): Show | 4 | HG02615.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-3659G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148836409 | ||||||
chr7:148837117
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.247-4367G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148837117 | ||||||
chr7:148837359
|
G | C | 1 | a0001c0001t0001g0002 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.247-4609C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148837359 | ||||||
chr7:148837425
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-4675C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148837425 | ||||||
chr7:148837464
|
G | A | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.247-4714C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148837464 | ||||||
chr7:148837492
|
C | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-4742G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148837492 | ||||||
chr7:148837587
|
A | T | 2 | a0001c0003t0001g0083a0001c0003t0001g0084 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.247-4837T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148837587 | ||||||
chr7:148837698
|
C | T | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.247-4948G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148837698 | ||||||
chr7:148837731
|
G | A | 1 | a0002c0002t0001g0328 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.247-4981C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148837731 | ||||||
chr7:148837874
|
G | A | 1 | a0002c0002t0001g0300 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.247-5124C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148837874 | ||||||
chr7:148838063
|
C | CT | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(240): Show | 245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.247-5314dupA | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148838063 | ||||||
chr7:148838063
|
C | CTT | 16 | a0001c0001t0001g0004a0001c0001t0001g0029a0001c0001t0001g0033others(13): Show | 16 | HG00140.hp2 HG00741.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.247-5315_247-5314d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148838063 | ||||||
chr7:148838284
|
G | A | 1 | a0001c0001t0002g0221 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.247-5534C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148838284 | ||||||
chr7:148838316
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0099 | 2 | HG01123.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.247-5566C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148838316 | ||||||
chr7:148838375
|
T | A | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108 | 3 | HG02055.hp2 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.247-5625A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148838375 | ||||||
chr7:148838439
|
G | A | 3 | a0001c0001t0001g0317a0001c0001t0001g0335a0001c0001t0001g0336 | 3 | HG00735.hp1 HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.247-5689C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148838439 | ||||||
chr7:148838479
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG02257.hp1 HG02886.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-5729T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148838479 | ||||||
chr7:148838494
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.247-5744C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148838494 | ||||||
chr7:148838647
|
G | A | 3 | a0001c0001t0001g0316a0001c0001t0001g0334a0001c0001t0006g0311 | 3 | HG02615.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.247-5897C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148838647 | ||||||
chr7:148838678
|
G | A | 1 | a0002c0002t0001g0347 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.247-5928C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148838678 | ||||||
chr7:148838778
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0002g0182 | 2 | HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.247-6028G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148838778 | ||||||
chr7:148838987
|
G | C | 1 | a0001c0001t0001g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.247-6237C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148838987 | ||||||
chr7:148839053
|
T | TAAGG | 37 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0028others(34): Show | 38 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.247-6307_247-6304d others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(1): Show |
100 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0020others(97): Show | 101 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.247-6311_247-6304d others(10): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(5): Show |
86 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0038others(83): Show | 86 | HG00280.hp1 HG00597.hp2 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.247-6315_247-6304d others(14): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(9): Show |
68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0025others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.247-6319_247-6304d others(18): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(13): Show |
18 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0074others(15): Show | 18 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.247-6323_247-6304d others(22): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(17): Show |
11 | a0001c0001t0001g0067a0001c0001t0001g0082a0001c0001t0001g0094others(8): Show | 11 | HG00544.hp2 HG01123.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.247-6327_247-6304d others(26): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(21): Show |
1 | a0001c0001t0001g0054 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.247-6331_247-6304d others(30): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(25): Show |
1 | a0001c0001t0001g0099 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.247-6335_247-6304d others(34): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(29): Show |
1 | a0001c0001t0002g0233 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.247-6339_247-6304d others(38): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(140): Show |
1 | a0002c0002t0001g0357 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.247-6304_247-6303i others(149): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(7): Show |
2 | a0001c0003t0001g0083a0001c0003t0001g0084 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.247-6304_247-6303i others(16): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(39): Show |
1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.247-6304_247-6303i others(48): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(43): Show |
1 | a0001c0001t0001g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.247-6304_247-6303i others(52): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(47): Show |
1 | a0001c0001t0001g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.247-6304_247-6303i others(56): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(55): Show |
1 | a0001c0001t0001g0014 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.247-6304_247-6303i others(64): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(59): Show |
3 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016 | 3 | HG03225.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.247-6304_247-6303i others(68): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
T | TAAGGAAG others(8): Show |
1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.247-6304_247-6303i others(17): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
TAAGGAAG others(5): Show |
T | 2 | a0001c0001t0001g0018a0001c0009t0001g0011 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.247-6315_247-6304d others(14): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839053
|
TAAGGAAG others(13): Show |
T | 8 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0088others(5): Show | 8 | HG00140.hp1 HG00639.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.247-6323_247-6304d others(22): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839053 | ||||||
chr7:148839061
|
G | GAAGGAGA others(15): Show |
1 | a0001c0001t0001g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.247-6312_247-6311i others(24): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839061 | ||||||
chr7:148839076
|
G | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.247-6326C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839076 | ||||||
chr7:148839088
|
G | A | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.247-6338C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839088 | ||||||
chr7:148839088
|
G | GGAAA | 5 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(2): Show | 5 | HG02615.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-6339_247-6338i others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839088 | ||||||
chr7:148839088
|
G | GGAAGGAA others(5): Show |
1 | a0001c0001t0001g0249 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.247-6339_247-6338i others(14): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839088 | ||||||
chr7:148839092
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.247-6342C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839092 | ||||||
chr7:148839106
|
A | AAGGAAGG others(4): Show |
1 | a0002c0002t0001g0331 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.247-6357_247-6356i others(13): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839106 | ||||||
chr7:148839107
|
A | AGGAAGGA others(3): Show |
2 | a0001c0001t0001g0126a0002c0002t0001g0297 | 2 | HG01106.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.247-6358_247-6357i others(12): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839107 | ||||||
chr7:148839107
|
A | AGGAAGGA others(9): Show |
1 | a0001c0001t0001g0183 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.247-6358_247-6357i others(18): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839107 | ||||||
chr7:148839114
|
T | C | 2 | a0001c0001t0001g0183a0001c0003t0001g0377 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.247-6364A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839114 | ||||||
chr7:148839152
|
C | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.247-6402G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839152 | ||||||
chr7:148839527
|
T | TG | 24 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0016others(21): Show | 24 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.247-6778dupC | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839527 | ||||||
chr7:148839527
|
TG | T | 65 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(62): Show | 65 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.247-6778delC | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839527 | ||||||
chr7:148839558
|
A | C | 1 | a0002c0002t0001g0341 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.247-6808T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839558 | ||||||
chr7:148839941
|
C | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+6529G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839941 | ||||||
chr7:148839943
|
A | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+6527T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839943 | ||||||
chr7:148839994
|
G | A | 27 | a0001c0001t0001g0046a0001c0001t0001g0143a0001c0001t0001g0144others(24): Show | 27 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.246+6476C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148839994 | ||||||
chr7:148840026
|
TG | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.246+6443delC | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148840026 | ||||||
chr7:148840338
|
A | T | 5 | a0001c0001t0001g0088a0001c0001t0001g0104a0001c0001t0001g0124others(2): Show | 5 | HG00140.hp1 HG00639.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+6132T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148840338 | ||||||
chr7:148840376
|
A | G | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.246+6094T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148840376 | ||||||
chr7:148840404
|
T | TA | 11 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(8): Show | 11 | HG01243.hp2 HG02280.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.246+6065dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148840404 | ||||||
chr7:148840455
|
A | G | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.246+6015T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148840455 | ||||||
chr7:148840887
|
T | C | 1 | a0001c0001t0001g0354 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.246+5583A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148840887 | ||||||
chr7:148840919
|
T | C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.246+5551A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148840919 | ||||||
chr7:148841125
|
A | G | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.246+5345T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148841125 | ||||||
chr7:148841155
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.246+5315T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148841155 | ||||||
chr7:148841181
|
CT | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.246+5288delA | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148841181 | ||||||
chr7:148841530
|
T | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(278): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.246+4940A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148841530 | ||||||
chr7:148841606
|
T | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+4864A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148841606 | ||||||
chr7:148841898
|
A | C | 10 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0057others(7): Show | 10 | NA18954.hp2 NA18965.hp1 NA18970.hp2 others(7): Show |
intron_variant | MODIFIER | c.246+4572T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148841898 | ||||||
chr7:148842117
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(4): Show | 7 | HG00738.hp1 HG01175.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+4353G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148842117 | ||||||
chr7:148842121
|
C | G | 1 | a0001c0001t0001g0144 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.246+4349G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148842121 | ||||||
chr7:148842141
|
G | A | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.246+4329C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148842141 | ||||||
chr7:148842231
|
T | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(278): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.246+4239A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148842231 | ||||||
chr7:148842252
|
T | C | 1 | a0001c0001t0001g0122 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.246+4218A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148842252 | ||||||
chr7:148842385
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.246+4085G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148842385 | ||||||
chr7:148842419
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0031 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.246+4051T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148842419 | ||||||
chr7:148842739
|
C | CAA | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+3729_246+3730d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148842739 | ||||||
chr7:148842882
|
A | G | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.246+3588T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148842882 | ||||||
chr7:148842935
|
C | T | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.246+3535G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148842935 | ||||||
chr7:148842936
|
G | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.246+3534C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148842936 | ||||||
chr7:148842956
|
C | T | 30 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0299others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.246+3514G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148842956 | ||||||
chr7:148843006
|
G | A | 1 | a0001c0009t0001g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.246+3464C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843006 | ||||||
chr7:148843037
|
A | T | 1 | a0001c0001t0001g0120 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.246+3433T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843037 | ||||||
chr7:148843064
|
C | T | 1 | a0001c0001t0001g0370 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.246+3406G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843064 | ||||||
chr7:148843123
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.246+3347C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843123 | ||||||
chr7:148843208
|
C | CA | 28 | a0001c0001t0001g0017a0001c0001t0001g0068a0001c0001t0001g0069others(25): Show | 28 | HG00735.hp2 HG01109.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.246+3261dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843208 | ||||||
chr7:148843208
|
CA | C | 14 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(11): Show | 14 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.246+3261delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843208 | ||||||
chr7:148843438
|
G | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(262): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.246+3032C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843438 | ||||||
chr7:148843583
|
G | GT | 42 | a0001c0001t0002g0007a0001c0001t0002g0009a0001c0001t0002g0010others(39): Show | 42 | HG00423.hp2 HG01081.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.246+2886dupA | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843583 | ||||||
chr7:148843583
|
G | GTT | 22 | a0001c0001t0002g0006a0001c0001t0002g0195a0001c0001t0002g0196others(19): Show | 22 | HG00544.hp2 HG00741.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.246+2885_246+2886d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843583 | ||||||
chr7:148843583
|
GTT | G | 16 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0085others(13): Show | 16 | HG00140.hp1 HG01168.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.246+2885_246+2886d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843583 | ||||||
chr7:148843583
|
GTTT | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(111): Show | 115 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.246+2884_246+2886d others(5): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843583 | ||||||
chr7:148843583
|
GTTTT | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(131): Show | 135 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.246+2883_246+2886d others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843583 | ||||||
chr7:148843583
|
GTTTTT | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG01243.hp2 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.246+2882_246+2886d others(7): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843583 | ||||||
chr7:148843589
|
T | G | 3 | a0001c0001t0002g0199a0001c0001t0002g0221a0001c0001t0002g0224 | 3 | HG00609.hp1 HG00621.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.246+2881A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843589 | ||||||
chr7:148843595
|
T | G | 1 | a0001c0001t0002g0223 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.246+2875A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843595 | ||||||
chr7:148843598
|
T | G | 1 | a0001c0009t0001g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.246+2872A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843598 | ||||||
chr7:148843602
|
T | G | 2 | a0001c0001t0001g0104a0001c0009t0001g0011 | 2 | HG01175.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.246+2868A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843602 | ||||||
chr7:148843618
|
C | T | 1 | a0001c0001t0002g0181 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.246+2852G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843618 | ||||||
chr7:148843619
|
A | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.246+2851T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843619 | ||||||
chr7:148843621
|
C | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.246+2849G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843621 | ||||||
chr7:148843634
|
C | T | 1 | a0001c0001t0002g0006 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.246+2836G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843634 | ||||||
chr7:148843689
|
A | G | 10 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.246+2781T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843689 | ||||||
chr7:148843726
|
G | C | 1 | a0001c0001t0002g0280 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.246+2744C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843726 | ||||||
chr7:148843744
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0124a0001c0001t0001g0130 | 3 | HG00140.hp1 HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.246+2726G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843744 | ||||||
chr7:148843838
|
G | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG02970.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.246+2632C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843838 | ||||||
chr7:148843859
|
T | C | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.246+2611A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843859 | ||||||
chr7:148843880
|
C | T | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.246+2590G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843880 | ||||||
chr7:148843949
|
TG | T | 7 | a0001c0001t0001g0296a0001c0001t0001g0299a0001c0001t0001g0302others(4): Show | 7 | HG00408.hp1 HG00642.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.246+2520delC | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148843949 | ||||||
chr7:148844071
|
TA | T | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.246+2398delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148844071 | ||||||
chr7:148844073
|
C | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0076a0001c0001t0001g0246 | 3 | HG00597.hp2 NA18966.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.246+2397G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148844073 | ||||||
chr7:148844417
|
G | A | 6 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG02717.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.246+2053C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148844417 | ||||||
chr7:148844569
|
C | T | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.246+1901G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148844569 | ||||||
chr7:148844592
|
A | G | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1878T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148844592 | ||||||
chr7:148844609
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.246+1861C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148844609 | ||||||
chr7:148844644
|
G | C | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.246+1826C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148844644 | ||||||
chr7:148844687
|
A | G | 13 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(10): Show | 13 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.246+1783T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148844687 | ||||||
chr7:148844693
|
G | A | 1 | a0001c0009t0001g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.246+1777C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148844693 | ||||||
chr7:148844802
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.246+1668G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148844802 | ||||||
chr7:148844842
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.246+1628C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148844842 | ||||||
chr7:148844894
|
C | T | 86 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0091others(83): Show | 86 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.246+1576G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148844894 | ||||||
chr7:148845034
|
G | C | 5 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(2): Show | 5 | HG00639.hp2 HG00738.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1436C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148845034 | ||||||
chr7:148845140
|
A | T | 1 | a0002c0002t0001g0348 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.246+1330T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148845140 | ||||||
chr7:148845218
|
T | C | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.246+1252A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148845218 | ||||||
chr7:148845406
|
A | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0091a0001c0001t0001g0172others(2): Show | 5 | HG01433.hp1 HG01978.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1064T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148845406 | ||||||
chr7:148845588
|
C | G | 1 | a0002c0002t0007g0378 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.246+882G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148845588 | ||||||
chr7:148845730
|
C | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(277): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.246+740G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148845730 | ||||||
chr7:148845748
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.246+722C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148845748 | ||||||
chr7:148845807
|
A | T | 1 | a0002c0002t0001g0348 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.246+663T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148845807 | ||||||
chr7:148846041
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01074.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.246+429C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148846041 | ||||||
chr7:148846110
|
C | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0091others(4): Show | 7 | HG01433.hp1 HG01952.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.246+360G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148846110 | ||||||
chr7:148846219
|
T | A | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.246+251A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148846219 | ||||||
chr7:148846219
|
T | TA | 3 | a0001c0001t0001g0316a0001c0001t0001g0334a0001c0001t0006g0311 | 3 | HG02615.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.246+250dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148846219 | ||||||
chr7:148846241
|
C | T | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.246+229G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148846241 | ||||||
chr7:148846291
|
A | C | 1 | a0003c0008t0002g0200 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.246+179T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148846291 | ||||||
chr7:148846433
|
A | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(277): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.246+37T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 3/19 | chr7 | 148846433 | ||||||
chr7:148846601
|
TA | T | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(278): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
splice_region_variant&intron_variant | LOW | c.118-4delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846601 | ||||||
chr7:148846661
|
C | T | 79 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(76): Show | 79 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.118-63G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846661 | ||||||
chr7:148846776
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.118-178T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846776 | ||||||
chr7:148846838
|
C | CTG | 9 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(6): Show | 9 | HG01167.hp1 HG01257.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.118-242_118-241dup others(2): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846838 | ||||||
chr7:148846838
|
CTG | C | 33 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0059others(30): Show | 33 | HG00423.hp2 HG00544.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.118-242_118-241del others(2): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846838 | ||||||
chr7:148846838
|
CTGTG | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(66): Show | 71 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.118-244_118-241del others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846838 | ||||||
chr7:148846838
|
CTGTGTG | C | 70 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0041others(67): Show | 70 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.118-246_118-241del others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846838 | ||||||
chr7:148846838
|
CTGTGTGT others(1): Show |
C | 83 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0030others(80): Show | 83 | HG00597.hp2 HG00642.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.118-248_118-241del others(8): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846838 | ||||||
chr7:148846838
|
CTGTGTGT others(3): Show |
C | 65 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0024others(62): Show | 65 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.118-250_118-241del others(10): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846838 | ||||||
chr7:148846838
|
CTGTGTGT others(5): Show |
C | 12 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(9): Show | 12 | HG00735.hp2 HG00738.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.118-252_118-241del others(12): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846838 | ||||||
chr7:148846838
|
CTGTGTGT others(7): Show |
C | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014 | 3 | HG02257.hp2 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.118-254_118-241del others(14): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846838 | ||||||
chr7:148846838
|
CTGTGTGT others(9): Show |
C | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-256_118-241del others(16): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846838 | ||||||
chr7:148846838
|
CTGTGTGT others(11): Show |
C | 3 | a0001c0001t0001g0316a0001c0001t0001g0334a0001c0001t0006g0311 | 3 | HG02615.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.118-258_118-241del others(18): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846838 | ||||||
chr7:148846844
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.118-246C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846844 | ||||||
chr7:148846848
|
G | C | 6 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG02717.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-250C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846848 | ||||||
chr7:148846865
|
TGTGTGTG others(12): Show |
T | 2 | a0001c0003t0001g0083a0001c0003t0001g0084 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.118-286_118-268del others(19): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846865 | ||||||
chr7:148846869
|
TGTGTGTG others(8): Show |
T | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.118-286_118-272del others(15): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846869 | ||||||
chr7:148846871
|
TGTGTGTG others(6): Show |
T | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.118-286_118-274del others(13): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846871 | ||||||
chr7:148846874
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.118-276C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846874 | ||||||
chr7:148846880
|
G | A | 1 | a0001c0001t0002g0280 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.118-282C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846880 | ||||||
chr7:148846885
|
T | A | 5 | a0001c0001t0001g0020a0001c0003t0001g0083a0001c0003t0001g0084others(2): Show | 5 | HG02647.hp1 HG02970.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-287A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846885 | ||||||
chr7:148846886
|
T | A | 1 | a0001c0001t0001g0063 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.118-288A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148846886 | ||||||
chr7:148847109
|
A | G | 1 | a0002c0002t0001g0348 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.117+73T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 2/19 | chr7 | 148847109 | ||||||
chr7:148847470
|
A | G | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-7-165T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148847470 | ||||||
chr7:148847523
|
A | C | 13 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(10): Show | 13 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7-218T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148847523 | ||||||
chr7:148847541
|
G | A | 1 | a0001c0001t0002g0215 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-7-236C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148847541 | ||||||
chr7:148847585
|
C | G | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-7-280G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148847585 | ||||||
chr7:148847589
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-7-284T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148847589 | ||||||
chr7:148847672
|
C | CATTAA | 4 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0003t0001g0377others(1): Show | 4 | HG02647.hp1 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-368_-7-367insTT others(3): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148847672 | ||||||
chr7:148847685
|
AG | A | 85 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0159others(82): Show | 85 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.-7-381delC | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148847685 | ||||||
chr7:148847827
|
T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-7-522A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148847827 | ||||||
chr7:148847921
|
A | G | 1 | a0002c0002t0001g0333 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-7-616T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148847921 | ||||||
chr7:148847989
|
T | G | 1 | a0001c0001t0001g0149 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-7-684A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148847989 | ||||||
chr7:148848171
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0080 | 2 | NA19001.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-7-866G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148848171 | ||||||
chr7:148848245
|
G | A | 1 | a0001c0001t0002g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-7-940C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148848245 | ||||||
chr7:148848433
|
T | A | 1 | a0001c0001t0001g0098 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-7-1128A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148848433 | ||||||
chr7:148848778
|
T | C | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7-1473A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148848778 | ||||||
chr7:148848790
|
G | C | 1 | a0001c0001t0001g0025 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-7-1485C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148848790 | ||||||
chr7:148848833
|
C | T | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7-1528G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148848833 | ||||||
chr7:148848845
|
C | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0091a0001c0001t0001g0159others(3): Show | 6 | HG01433.hp1 HG01978.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-1540G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148848845 | ||||||
chr7:148848904
|
C | G | 34 | a0002c0002t0001g0297a0002c0002t0001g0300a0002c0002t0001g0301others(31): Show | 34 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.-7-1599G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148848904 | ||||||
chr7:148848936
|
T | A | 1 | a0001c0001t0001g0148 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-7-1631A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148848936 | ||||||
chr7:148849149
|
T | C | 2 | a0001c0003t0001g0377a0001c0007t0001g0376 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-7-1844A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148849149 | ||||||
chr7:148849238
|
G | C | 1 | a0001c0001t0001g0109 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-7-1933C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148849238 | ||||||
chr7:148849254
|
G | A | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7-1949C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148849254 | ||||||
chr7:148849985
|
T | C | 1 | a0001c0001t0002g0273 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-7-2680A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148849985 | ||||||
chr7:148850064
|
G | A | 1 | a0001c0001t0002g0227 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-7-2759C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148850064 | ||||||
chr7:148850611
|
T | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-3306A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148850611 | ||||||
chr7:148850659
|
C | T | 1 | a0001c0001t0002g0215 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-7-3354G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148850659 | ||||||
chr7:148850776
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-7-3471C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148850776 | ||||||
chr7:148850834
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0289 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-7-3529C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148850834 | ||||||
chr7:148850969
|
A | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0166 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-7-3664T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148850969 | ||||||
chr7:148851252
|
C | A | 5 | a0001c0001t0002g0266a0001c0001t0002g0270a0001c0001t0002g0271others(2): Show | 5 | NA18951.hp1 NA18993.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-3947G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148851252 | ||||||
chr7:148851274
|
T | C | 3 | a0001c0001t0001g0304a0001c0001t0001g0324a0001c0001t0001g0325 | 3 | HG00609.hp2 NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-7-3969A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148851274 | ||||||
chr7:148851301
|
C | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(277): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.-7-3996G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148851301 | ||||||
chr7:148851344
|
C | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0031 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-7-4039G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148851344 | ||||||
chr7:148851356
|
T | G | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-7-4051A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148851356 | ||||||
chr7:148851495
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-7-4190C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148851495 | ||||||
chr7:148851700
|
A | G | 1 | a0001c0001t0002g0188 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-7-4395T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148851700 | ||||||
chr7:148852054
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0190a0001c0001t0001g0193others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-4749G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148852054 | ||||||
chr7:148852077
|
T | C | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7-4772A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148852077 | ||||||
chr7:148852308
|
C | T | 10 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(7): Show | 10 | HG02055.hp1 HG02572.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-7-5003G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148852308 | ||||||
chr7:148852310
|
T | C | 3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0007t0001g0376 | 3 | HG02647.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-7-5005A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148852310 | ||||||
chr7:148852562
|
TGCAATGC others(8): Show |
T | 3 | a0001c0001t0001g0141a0001c0001t0001g0190a0001c0001t0001g0193 | 3 | HG01884.hp2 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-7-5272_-7-5258del others(15): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148852562 | ||||||
chr7:148852633
|
CT | C | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-5329delA | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148852633 | ||||||
chr7:148852679
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(4): Show | 7 | HG00738.hp1 HG01175.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-5374G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148852679 | ||||||
chr7:148852921
|
C | G | 3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0007t0001g0376 | 3 | HG02647.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-7-5616G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148852921 | ||||||
chr7:148852927
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-7-5622C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148852927 | ||||||
chr7:148853138
|
G | C | 4 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0003t0001g0377others(1): Show | 4 | HG02647.hp1 HG02970.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-5833C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148853138 | ||||||
chr7:148853328
|
C | T | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7-6023G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148853328 | ||||||
chr7:148853479
|
T | C | 3 | a0001c0001t0001g0252a0001c0001t0001g0254a0001c0005t0001g0253 | 3 | HG02055.hp1 HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-7-6174A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148853479 | ||||||
chr7:148853482
|
G | A | 1 | a0003c0008t0002g0200 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-7-6177C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148853482 | ||||||
chr7:148853653
|
A | T | 1 | a0002c0002t0001g0344 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-7-6348T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148853653 | ||||||
chr7:148853715
|
A | AGTATGTA others(16): Show |
1 | a0001c0001t0002g0280 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-7-6433_-7-6411dup others(23): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148853715 | ||||||
chr7:148854033
|
T | G | 1 | a0001c0001t0002g0258 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-7-6728A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148854033 | ||||||
chr7:148854143
|
T | C | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055 | 3 | HG02818.hp2 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-7-6838A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148854143 | ||||||
chr7:148854241
|
CG | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-7-6937delC | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148854241 | ||||||
chr7:148854329
|
G | A | 3 | a0001c0001t0001g0190a0001c0001t0001g0193a0001c0001t0001g0289 | 3 | HG01884.hp2 HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-7-7024C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148854329 | ||||||
chr7:148854349
|
T | TG | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-7045dupC | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148854349 | ||||||
chr7:148854385
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-7-7080C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148854385 | ||||||
chr7:148854414
|
C | T | 2 | a0001c0001t0001g0353a0001c0001t0001g0354 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-7-7109G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148854414 | ||||||
chr7:148854435
|
C | CA | 38 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(35): Show | 40 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.-7-7131dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148854435 | ||||||
chr7:148854558
|
T | A | 1 | a0001c0001t0001g0255 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-7-7253A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148854558 | ||||||
chr7:148854983
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-7-7678T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148854983 | ||||||
chr7:148855084
|
G | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-7-7779C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855084 | ||||||
chr7:148855111
|
C | T | 75 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-7-7806G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855111 | ||||||
chr7:148855275
|
A | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-7970T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855275 | ||||||
chr7:148855364
|
C | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(276): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-7-8059G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855364 | ||||||
chr7:148855385
|
T | G | 1 | a0001c0001t0001g0255 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-7-8080A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855385 | ||||||
chr7:148855531
|
T | C | 15 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(12): Show | 15 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7-8226A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855531 | ||||||
chr7:148855539
|
A | C | 5 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-8234T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855539 | ||||||
chr7:148855665
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG00741.hp2 HG01978.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-7-8360G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855665 | ||||||
chr7:148855681
|
T | C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-7-8376A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855681 | ||||||
chr7:148855727
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-7-8422C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855727 | ||||||
chr7:148855804
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7-8499T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855804 | ||||||
chr7:148855812
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0078 | 2 | NA18955.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-7-8507G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855812 | ||||||
chr7:148855854
|
C | T | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7-8549G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855854 | ||||||
chr7:148855897
|
C | CA | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0020others(86): Show | 91 | HG00140.hp1 HG00597.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.-7-8593dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855897 | ||||||
chr7:148855897
|
C | CAA | 15 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(12): Show | 15 | HG00642.hp1 HG01074.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7-8594_-7-8593dup others(2): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855897 | ||||||
chr7:148855897
|
CA | C | 14 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0001g0095others(11): Show | 14 | HG00423.hp2 HG01070.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7-8593delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855897 | ||||||
chr7:148855928
|
A | G | 1 | a0001c0009t0001g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-7-8623T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148855928 | ||||||
chr7:148856090
|
A | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026 | 3 | HG00738.hp1 HG01175.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-7-8785T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148856090 | ||||||
chr7:148856096
|
T | C | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7-8791A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148856096 | ||||||
chr7:148856128
|
C | T | 16 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0085others(13): Show | 16 | HG01433.hp1 HG01891.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.-7-8823G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148856128 | ||||||
chr7:148856135
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-7-8830C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148856135 | ||||||
chr7:148856286
|
T | C | 1 | a0003c0008t0002g0200 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-7-8981A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148856286 | ||||||
chr7:148856404
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0036 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-7-9099G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148856404 | ||||||
chr7:148856508
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02809.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-7-9203C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148856508 | ||||||
chr7:148856573
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-7-9268A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148856573 | ||||||
chr7:148856718
|
A | G | 27 | a0001c0001t0001g0046a0001c0001t0001g0143a0001c0001t0001g0144others(24): Show | 27 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-7-9413T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148856718 | ||||||
chr7:148856738
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-7-9433A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148856738 | ||||||
chr7:148856945
|
G | C | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7-9640C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148856945 | ||||||
chr7:148857002
|
A | C | 5 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-9697T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148857002 | ||||||
chr7:148857018
|
T | C | 1 | a0001c0001t0001g0361 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-7-9713A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148857018 | ||||||
chr7:148857032
|
T | C | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7-9727A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148857032 | ||||||
chr7:148857153
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-7-9848C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148857153 | ||||||
chr7:148857243
|
A | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(164): Show | 169 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(166): Show |
intron_variant | MODIFIER | c.-7-9938T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148857243 | ||||||
chr7:148857317
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-7-10012T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148857317 | ||||||
chr7:148857343
|
A | G | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-7-10038T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148857343 | ||||||
chr7:148857681
|
G | A | 1 | a0001c0001t0002g0269 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-7-10376C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148857681 | ||||||
chr7:148857692
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(118): Show | 123 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.-7-10387T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148857692 | ||||||
chr7:148857702
|
G | A | 70 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(67): Show | 70 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.-7-10397C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148857702 | ||||||
chr7:148857730
|
G | A | 7 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0093others(4): Show | 7 | HG02630.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-10425C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148857730 | ||||||
chr7:148857750
|
CAAATAAA others(1): Show |
C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-7-10453_-7-10446d others(10): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148857750 | ||||||
chr7:148857991
|
T | TA | 25 | a0001c0001t0001g0102a0001c0001t0001g0116a0001c0001t0001g0117others(22): Show | 25 | HG00741.hp1 HG01081.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.-7-10687dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148857991 | ||||||
chr7:148857991
|
TA | T | 8 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 8 | HG02109.hp1 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-10687delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148857991 | ||||||
chr7:148858030
|
C | T | 3 | a0002c0002t0001g0342a0002c0002t0001g0347a0002c0004t0001g0346 | 3 | HG00280.hp1 HG01257.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-7-10725G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858030 | ||||||
chr7:148858208
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-7-10903G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858208 | ||||||
chr7:148858209
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-10904C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858209 | ||||||
chr7:148858216
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-10911G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858216 | ||||||
chr7:148858291
|
C | CA | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(142): Show | 147 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.-7-10987dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858291 | ||||||
chr7:148858341
|
T | A | 1 | a0001c0001t0002g0198 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-7-11036A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858341 | ||||||
chr7:148858398
|
C | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0020others(83): Show | 88 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.-7-11093G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858398 | ||||||
chr7:148858510
|
A | G | 1 | a0001c0001t0002g0280 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-7-11205T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858510 | ||||||
chr7:148858517
|
A | T | 1 | a0001c0001t0002g0280 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-7-11212T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858517 | ||||||
chr7:148858531
|
A | G | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-11226T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858531 | ||||||
chr7:148858535
|
T | A | 1 | a0001c0001t0002g0280 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-7-11230A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858535 | ||||||
chr7:148858564
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG02132.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-7-11259C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858564 | ||||||
chr7:148858571
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7-11266G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858571 | ||||||
chr7:148858679
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG00741.hp2 HG01978.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-7-11374G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858679 | ||||||
chr7:148858700
|
T | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(144): Show | 149 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.-7-11395A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148858700 | ||||||
chr7:148859245
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-7-11940G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148859245 | ||||||
chr7:148859279
|
G | C | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7-11974C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148859279 | ||||||
chr7:148859409
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-7-12104C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148859409 | ||||||
chr7:148859505
|
A | AAAC | 89 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0028others(86): Show | 89 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.-7-12203_-7-12201d others(5): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148859505 | ||||||
chr7:148859505
|
A | AAACAAC | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(124): Show | 129 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.-7-12206_-7-12201d others(8): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148859505 | ||||||
chr7:148859505
|
A | AAACAACA others(2): Show |
21 | a0001c0001t0001g0022a0001c0001t0001g0048a0001c0001t0001g0049others(18): Show | 21 | HG00280.hp1 HG00639.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7-12209_-7-12201d others(11): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148859505 | ||||||
chr7:148859505
|
A | AAACAACA others(5): Show |
2 | a0001c0001t0001g0047a0001c0001t0001g0055 | 2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-7-12212_-7-12201d others(14): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148859505 | ||||||
chr7:148859505
|
AAAC | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0085others(2): Show | 5 | HG00738.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-12203_-7-12201d others(5): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148859505 | ||||||
chr7:148859505
|
AAACAAC | A | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7-12206_-7-12201d others(8): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148859505 | ||||||
chr7:148859505
|
AAACAACA others(2): Show |
A | 7 | a0001c0001t0002g0010a0001c0001t0002g0198a0001c0001t0002g0206others(4): Show | 7 | HG02056.hp1 NA18953.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7-12209_-7-12201d others(11): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148859505 | ||||||
chr7:148859539
|
G | A | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7-12234C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148859539 | ||||||
chr7:148859597
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02155.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-7-12292T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148859597 | ||||||
chr7:148859651
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-7-12346C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148859651 | ||||||
chr7:148859877
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-7-12572T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148859877 | ||||||
chr7:148860009
|
T | TA | 3 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0125 | 3 | HG01106.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-7-12705_-7-12704i others(3): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148860009 | ||||||
chr7:148860010
|
T | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(272): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-7-12705A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148860010 | ||||||
chr7:148860109
|
C | T | 377 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(374): Show | 379 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.-7-12804G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148860109 | ||||||
chr7:148860327
|
T | C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-7-13022A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148860327 | ||||||
chr7:148860332
|
GA | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(270): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.-7-13028delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148860332 | ||||||
chr7:148860364
|
T | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0078 | 2 | NA18955.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.-7-13059A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148860364 | ||||||
chr7:148860450
|
C | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(5): Show | 8 | HG00738.hp1 HG01175.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-13145G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148860450 | ||||||
chr7:148860538
|
AAAGT | A | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-13237_-7-13234d others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148860538 | ||||||
chr7:148860668
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-7-13363T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148860668 | ||||||
chr7:148860720
|
G | A | 2 | a0001c0001t0002g0210a0001c0001t0002g0211 | 2 | HG00423.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-7-13415C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148860720 | ||||||
chr7:148860764
|
T | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-13459A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148860764 | ||||||
chr7:148860808
|
A | C | 2 | a0001c0001t0002g0263a0001c0001t0002g0265 | 2 | NA18943.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-7-13503T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148860808 | ||||||
chr7:148860905
|
TCAAA | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-13604_-7-13601d others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148860905 | ||||||
chr7:148861032
|
G | T | 1 | a0001c0001t0001g0319 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-7-13727C>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861032 | ||||||
chr7:148861035
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0190a0001c0001t0001g0193others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-13730C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861035 | ||||||
chr7:148861091
|
T | A | 1 | a0001c0001t0001g0145 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-7-13786A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861091 | ||||||
chr7:148861198
|
T | G | 1 | a0001c0001t0001g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-13893A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861198 | ||||||
chr7:148861228
|
CT | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(184): Show | 189 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(186): Show |
intron_variant | MODIFIER | c.-7-13924delA | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861228 | ||||||
chr7:148861288
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-7-13983C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861288 | ||||||
chr7:148861325
|
C | G | 1 | a0001c0001t0002g0201 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-7-14020G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861325 | ||||||
chr7:148861381
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-7-14076G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861381 | ||||||
chr7:148861458
|
C | T | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-7-14153G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861458 | ||||||
chr7:148861556
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-7-14251G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861556 | ||||||
chr7:148861754
|
T | G | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7-14449A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861754 | ||||||
chr7:148861802
|
T | TA | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-14498_-7-14497i others(3): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861802 | ||||||
chr7:148861803
|
T | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(5): Show | 8 | HG00738.hp1 HG01175.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-14498A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861803 | ||||||
chr7:148861803
|
T | TA | 43 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(40): Show | 43 | HG00673.hp1 HG01099.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.-7-14499dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861803 | ||||||
chr7:148861803
|
T | TAA | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(194): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-7-14500_-7-14499d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861803 | ||||||
chr7:148861803
|
T | TAAA | 16 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(13): Show | 16 | HG01081.hp2 HG01109.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.-7-14501_-7-14499d others(5): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861803 | ||||||
chr7:148861803
|
TA | T | 9 | a0001c0001t0002g0007a0001c0001t0002g0210a0001c0001t0002g0212others(6): Show | 9 | HG01192.hp1 HG03704.hp2 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-14499delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861803 | ||||||
chr7:148861818
|
A | T | 1 | a0001c0001t0002g0279 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-7-14513T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861818 | ||||||
chr7:148861819
|
A | T | 1 | a0001c0001t0002g0279 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-7-14514T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861819 | ||||||
chr7:148861896
|
C | A | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7-14591G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861896 | ||||||
chr7:148861929
|
T | A | 1 | a0001c0001t0002g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-7-14624A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861929 | ||||||
chr7:148861979
|
G | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(165): Show | 170 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(167): Show |
intron_variant | MODIFIER | c.-7-14674C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148861979 | ||||||
chr7:148862210
|
CACATTA | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026 | 3 | HG00738.hp1 HG01175.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-7-14911_-7-14906d others(8): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148862210 | ||||||
chr7:148862298
|
C | G | 1 | a0001c0001t0001g0289 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-7-14993G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148862298 | ||||||
chr7:148862315
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0030 | 2 | HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-7-15010C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148862315 | ||||||
chr7:148862690
|
A | T | 1 | a0001c0001t0002g0202 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-7-15385T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148862690 | ||||||
chr7:148862805
|
A | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-15500T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148862805 | ||||||
chr7:148862894
|
G | T | 1 | a0001c0010t0003g0003 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-7-15589C>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148862894 | ||||||
chr7:148862923
|
G | GTTTTGT | 80 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-7-15619_-7-15618i others(8): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148862923 | ||||||
chr7:148862931
|
A | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0184a0001c0001t0001g0185others(10): Show | 13 | HG02055.hp1 HG02155.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-15626T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148862931 | ||||||
chr7:148862976
|
T | C | 80 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-7-15671A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148862976 | ||||||
chr7:148863083
|
CA | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 284 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(281): Show |
intron_variant | MODIFIER | c.-7-15779delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148863083 | ||||||
chr7:148863096
|
A | AAAGAAAG | 80 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-7-15792_-7-15791i others(9): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148863096 | ||||||
chr7:148863096
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-7-15791T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148863096 | ||||||
chr7:148863189
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-15884C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148863189 | ||||||
chr7:148863195
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-7-15890C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148863195 | ||||||
chr7:148863212
|
C | T | 6 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0093others(3): Show | 6 | HG02717.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-15907G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148863212 | ||||||
chr7:148863298
|
C | A | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7-15993G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148863298 | ||||||
chr7:148863532
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0002g0182 | 2 | HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-7-16227A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148863532 | ||||||
chr7:148863534
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-7-16229G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148863534 | ||||||
chr7:148863587
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026 | 3 | HG00738.hp1 HG01175.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-7-16282G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148863587 | ||||||
chr7:148863937
|
G | C | 84 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-7-16632C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148863937 | ||||||
chr7:148863966
|
T | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026 | 3 | HG00738.hp1 HG01175.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-7-16661A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148863966 | ||||||
chr7:148864010
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-7-16705T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148864010 | ||||||
chr7:148864232
|
T | C | 79 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(76): Show | 79 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.-7-16927A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148864232 | ||||||
chr7:148864232
|
T | G | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-7-16927A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148864232 | ||||||
chr7:148864324
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0166 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-7-17019C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148864324 | ||||||
chr7:148864342
|
T | C | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG00741.hp2 HG01978.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-7-17037A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148864342 | ||||||
chr7:148864494
|
A | G | 84 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-7-17189T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148864494 | ||||||
chr7:148864500
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-17195A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148864500 | ||||||
chr7:148864542
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0054 | 2 | HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-7-17237C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148864542 | ||||||
chr7:148864683
|
C | CA | 85 | a0001c0001t0001g0037a0001c0001t0001g0058a0001c0001t0001g0099others(82): Show | 85 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.-7-17379dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148864683 | ||||||
chr7:148864683
|
C | CAA | 23 | a0001c0001t0001g0169a0001c0001t0001g0184a0001c0001t0001g0185others(20): Show | 23 | HG02055.hp1 HG02056.hp2 HG02135.hp1 others(20): Show |
intron_variant | MODIFIER | c.-7-17380_-7-17379d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148864683 | ||||||
chr7:148864725
|
G | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0055 | 2 | HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-7-17420C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148864725 | ||||||
chr7:148864913
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-7-17608C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148864913 | ||||||
chr7:148864945
|
G | A | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-7-17640C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148864945 | ||||||
chr7:148865067
|
C | T | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7-17762G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865067 | ||||||
chr7:148865069
|
T | G | 84 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-7-17764A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865069 | ||||||
chr7:148865125
|
C | CA | 15 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0001g0041others(12): Show | 15 | HG01106.hp2 HG01978.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7-17821dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865125 | ||||||
chr7:148865125
|
CA | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0018others(5): Show | 8 | HG01074.hp1 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-17821delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865125 | ||||||
chr7:148865125
|
CAAA | C | 80 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-7-17823_-7-17821d others(5): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865125 | ||||||
chr7:148865152
|
A | T | 1 | a0001c0001t0001g0125 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-7-17847T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865152 | ||||||
chr7:148865250
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-7-17945C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865250 | ||||||
chr7:148865451
|
A | C | 84 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-7-18146T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865451 | ||||||
chr7:148865557
|
T | G | 5 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-18252A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865557 | ||||||
chr7:148865564
|
C | A | 1 | a0001c0001t0001g0332 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-7-18259G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865564 | ||||||
chr7:148865676
|
C | A | 1 | a0001c0001t0002g0188 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-7-18371G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865676 | ||||||
chr7:148865843
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(144): Show | 149 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.-8+18321A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865843 | ||||||
chr7:148865883
|
A | C | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+18281T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865883 | ||||||
chr7:148865898
|
G | A | 1 | a0001c0009t0001g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-8+18266C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865898 | ||||||
chr7:148865947
|
A | C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8+18217T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148865947 | ||||||
chr7:148866031
|
C | G | 1 | a0001c0003t0001g0083 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-8+18133G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866031 | ||||||
chr7:148866061
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-8+18103A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866061 | ||||||
chr7:148866124
|
T | C | 1 | a0001c0001t0001g0370 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-8+18040A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866124 | ||||||
chr7:148866209
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8+17955G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866209 | ||||||
chr7:148866222
|
G | A | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8+17942C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866222 | ||||||
chr7:148866291
|
G | A | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+17873C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866291 | ||||||
chr7:148866301
|
A | G | 84 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+17863T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866301 | ||||||
chr7:148866475
|
C | G | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8+17689G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866475 | ||||||
chr7:148866491
|
A | AATATATA others(29): Show |
20 | a0001c0001t0001g0085a0001c0001t0001g0092a0001c0001t0001g0093others(17): Show | 20 | HG02055.hp1 HG02109.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8+17637_-8+17672d others(38): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866491 | ||||||
chr7:148866501
|
C | T | 1 | a0001c0001t0001g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-8+17663G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866501 | ||||||
chr7:148866501
|
CGTATATA others(11): Show |
C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8+17645_-8+17662d others(20): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866501 | ||||||
chr7:148866502
|
GTATATAC others(47): Show |
G | 80 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-8+17608_-8+17661d others(56): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866502 | ||||||
chr7:148866518
|
G | A | 7 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0183others(4): Show | 7 | HG02647.hp1 HG02970.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+17646C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866518 | ||||||
chr7:148866519
|
T | C | 6 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0183others(3): Show | 6 | HG02647.hp1 HG02970.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+17645A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866519 | ||||||
chr7:148866519
|
T | TGTATATA others(11): Show |
35 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(32): Show | 37 | HG00140.hp1 HG00639.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.-8+17627_-8+17644d others(20): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866519 | ||||||
chr7:148866520
|
G | A | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17644C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866520 | ||||||
chr7:148866527
|
C | CAT | 3 | a0001c0001t0001g0149a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG01070.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-8+17635_-8+17636d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866527 | ||||||
chr7:148866527
|
C | T | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17637G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866527 | ||||||
chr7:148866528
|
A | ATATATAT others(11): Show |
5 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(2): Show | 5 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+17635_-8+17636i others(20): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866528 | ||||||
chr7:148866532
|
A | G | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17632T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866532 | ||||||
chr7:148866533
|
T | C | 2 | a0001c0006t0002g0264a0001c0007t0001g0376 | 2 | HG02970.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-8+17631A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866533 | ||||||
chr7:148866538
|
GTATATAC others(11): Show |
G | 8 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(5): Show | 8 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+17608_-8+17625d others(20): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866538 | ||||||
chr7:148866542
|
A | G | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17622T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866542 | ||||||
chr7:148866545
|
C | T | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17619G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866545 | ||||||
chr7:148866545
|
CATATATA others(13): Show |
C | 3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0007t0001g0376 | 3 | HG02647.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+17599_-8+17618d others(22): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866545 | ||||||
chr7:148866554
|
A | G | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17610T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866554 | ||||||
chr7:148866556
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(193): Show | 198 | HG00140.hp1 HG00597.hp2 HG00621.hp2 others(195): Show |
intron_variant | MODIFIER | c.-8+17608T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866556 | ||||||
chr7:148866572
|
A | G | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17592T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866572 | ||||||
chr7:148866573
|
C | T | 1 | a0001c0001t0002g0188 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-8+17591G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866573 | ||||||
chr7:148866574
|
G | A | 4 | a0001c0001t0001g0316a0001c0001t0001g0334a0001c0001t0006g0311others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+17590C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866574 | ||||||
chr7:148866579
|
T | C | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17585A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866579 | ||||||
chr7:148866580
|
A | G | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17584T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866580 | ||||||
chr7:148866581
|
C | T | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17583G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866581 | ||||||
chr7:148866600
|
A | G | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17564T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866600 | ||||||
chr7:148866612
|
A | G | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17552T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866612 | ||||||
chr7:148866619
|
T | C | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17545A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866619 | ||||||
chr7:148866621
|
C | T | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17543G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866621 | ||||||
chr7:148866627
|
T | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0147a0001c0001t0001g0148others(4): Show | 7 | HG01928.hp2 HG01934.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+17537A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866627 | ||||||
chr7:148866628
|
G | A | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17536C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866628 | ||||||
chr7:148866630
|
A | G | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17534T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866630 | ||||||
chr7:148866631
|
T | TATATAC | 10 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+17527_-8+17532d others(8): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866631 | ||||||
chr7:148866639
|
T | C | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17525A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866639 | ||||||
chr7:148866649
|
C | T | 2 | a0001c0006t0002g0264a0001c0007t0001g0376 | 2 | HG02970.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-8+17515G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866649 | ||||||
chr7:148866654
|
ATACGTAT others(13): Show |
A | 1 | a0001c0001t0002g0209 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-8+17490_-8+17509d others(22): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866654 | ||||||
chr7:148866670
|
A | T | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17494T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866670 | ||||||
chr7:148866672
|
A | T | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17492T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866672 | ||||||
chr7:148866673
|
TGTACGTA others(190): Show |
T | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17294_-8+17490d others(2): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866673 | ||||||
chr7:148866678
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-8+17486C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866678 | ||||||
chr7:148866678
|
GTATATGC others(13): Show |
G | 3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0007t0001g0376 | 3 | HG02647.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+17466_-8+17485d others(22): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866678 | ||||||
chr7:148866698
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0091 | 2 | HG01433.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-8+17466T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866698 | ||||||
chr7:148866705
|
C | CAT | 11 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(8): Show | 11 | HG02145.hp1 HG02280.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+17457_-8+17458d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866705 | ||||||
chr7:148866705
|
CAT | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG02257.hp1 HG02886.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+17457_-8+17458d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866705 | ||||||
chr7:148866869
|
C | T | 7 | a0001c0001t0002g0262a0001c0001t0002g0263a0001c0001t0002g0265others(4): Show | 7 | HG00544.hp2 NA18943.hp1 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+17295G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866869 | ||||||
chr7:148866871
|
C | T | 11 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0057others(8): Show | 11 | HG02976.hp2 NA18954.hp2 NA18965.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+17293G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866871 | ||||||
chr7:148866876
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-8+17288C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866876 | ||||||
chr7:148866881
|
A | G | 1 | a0001c0006t0002g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-8+17283T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866881 | ||||||
chr7:148866960
|
C | T | 2 | a0001c0001t0002g0210a0001c0001t0002g0211 | 2 | HG00423.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-8+17204G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866960 | ||||||
chr7:148866966
|
A | G | 84 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+17198T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866966 | ||||||
chr7:148866994
|
G | A | 4 | a0001c0001t0001g0096a0001c0003t0001g0083a0001c0003t0001g0084others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+17170C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148866994 | ||||||
chr7:148867019
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-8+17145G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148867019 | ||||||
chr7:148867046
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-8+17118C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148867046 | ||||||
chr7:148867275
|
G | A | 34 | a0002c0002t0001g0297a0002c0002t0001g0300a0002c0002t0001g0301others(31): Show | 34 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.-8+16889C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148867275 | ||||||
chr7:148867292
|
G | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(10): Show | 13 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8+16872C>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148867292 | ||||||
chr7:148867442
|
T | C | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+16722A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148867442 | ||||||
chr7:148867557
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-8+16607C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148867557 | ||||||
chr7:148867660
|
G | C | 1 | a0001c0001t0001g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-8+16504C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148867660 | ||||||
chr7:148867815
|
G | C | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-8+16349C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148867815 | ||||||
chr7:148867857
|
G | A | 3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0007t0001g0376 | 3 | HG02647.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+16307C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148867857 | ||||||
chr7:148867998
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-8+16166G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148867998 | ||||||
chr7:148868057
|
A | C | 1 | a0001c0001t0002g0288 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-8+16107T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868057 | ||||||
chr7:148868126
|
C | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0190a0001c0001t0001g0193others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+16038G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868126 | ||||||
chr7:148868202
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-8+15962C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868202 | ||||||
chr7:148868252
|
G | A | 2 | a0002c0002t0001g0342a0002c0002t0001g0347 | 2 | HG00280.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-8+15912C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868252 | ||||||
chr7:148868449
|
CTCACGAG others(9): Show |
C | 1 | a0001c0001t0001g0105 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-8+15699_-8+15714d others(18): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868449 | ||||||
chr7:148868469
|
C | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+15695G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868469 | ||||||
chr7:148868470
|
G | A | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8+15694C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868470 | ||||||
chr7:148868540
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(139): Show | 144 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8+15624G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868540 | ||||||
chr7:148868557
|
G | A | 80 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-8+15607C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868557 | ||||||
chr7:148868571
|
G | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-8+15593C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868571 | ||||||
chr7:148868676
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-8+15488G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868676 | ||||||
chr7:148868792
|
T | C | 1 | a0001c0001t0002g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-8+15372A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868792 | ||||||
chr7:148868854
|
T | A | 2 | a0001c0003t0001g0083a0001c0003t0001g0084 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+15310A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868854 | ||||||
chr7:148868882
|
C | T | 3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0007t0001g0376 | 3 | HG02647.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+15282G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868882 | ||||||
chr7:148868898
|
T | A | 3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0007t0001g0376 | 3 | HG02647.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+15266A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868898 | ||||||
chr7:148868932
|
T | TA | 84 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+15231dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148868932 | ||||||
chr7:148869134
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-8+15030C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869134 | ||||||
chr7:148869198
|
A | AATGCCAG others(583): Show |
5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+14965_-8+14966i others(592): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869198 | ||||||
chr7:148869244
|
A | G | 2 | a0002c0002t0001g0333a0002c0002t0001g0343 | 2 | HG00673.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-8+14920T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869244 | ||||||
chr7:148869302
|
A | G | 1 | a0002c0002t0001g0301 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-8+14862T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869302 | ||||||
chr7:148869322
|
T | C | 1 | a0002c0002t0001g0315 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-8+14842A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869322 | ||||||
chr7:148869338
|
C | CT | 18 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0091others(15): Show | 18 | HG00621.hp1 HG01358.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.-8+14825dupA | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869338 | ||||||
chr7:148869338
|
C | CTT | 9 | a0001c0001t0001g0026a0001c0001t0002g0195a0001c0001t0002g0198others(6): Show | 9 | HG00738.hp1 HG01981.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+14824_-8+14825d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869338 | ||||||
chr7:148869338
|
C | CTTTTTTT others(585): Show |
2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-8+14825_-8+14826i others(594): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869338 | ||||||
chr7:148869338
|
C | CTTTTTTT others(586): Show |
1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8+14825_-8+14826i others(595): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869338 | ||||||
chr7:148869338
|
CT | C | 74 | a0001c0001t0001g0016a0001c0001t0001g0048a0001c0001t0001g0054others(71): Show | 74 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.-8+14825delA | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869338 | ||||||
chr7:148869338
|
CTT | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0024others(42): Show | 45 | HG00597.hp2 HG00642.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.-8+14824_-8+14825d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869338 | ||||||
chr7:148869338
|
CTTT | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0020others(124): Show | 129 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(126): Show |
intron_variant | MODIFIER | c.-8+14823_-8+14825d others(5): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869338 | ||||||
chr7:148869448
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-8+14716G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869448 | ||||||
chr7:148869503
|
A | G | 2 | a0001c0001t0002g0278a0001c0001t0002g0281 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-8+14661T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869503 | ||||||
chr7:148869573
|
A | AGCAATCC others(586): Show |
1 | a0001c0001t0001g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-8+14590_-8+14591i others(595): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869573 | ||||||
chr7:148869573
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8+14591T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869573 | ||||||
chr7:148869593
|
C | CGCTCAAA others(582): Show |
2 | a0001c0001t0001g0254a0001c0005t0001g0253 | 2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-8+14570_-8+14571i others(591): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869593 | ||||||
chr7:148869593
|
C | CGCTCAAA others(583): Show |
1 | a0001c0001t0001g0252 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-8+14570_-8+14571i others(592): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869593 | ||||||
chr7:148869593
|
C | CGCTCAAA others(587): Show |
1 | a0001c0001t0001g0255 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-8+14570_-8+14571i others(596): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869593 | ||||||
chr7:148869593
|
C | CGCTCAAA others(588): Show |
2 | a0001c0001t0001g0249a0001c0001t0001g0251 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-8+14570_-8+14571i others(597): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869593 | ||||||
chr7:148869593
|
C | CGCTCAAA others(1182): Show |
1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-8+14570_-8+14571i others(1191): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869593 | ||||||
chr7:148869593
|
C | CGCTCAAA others(1183): Show |
1 | a0001c0001t0001g0185 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-8+14570_-8+14571i others(1192): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869593 | ||||||
chr7:148869593
|
C | CGCTCAAA others(589): Show |
2 | a0001c0001t0001g0248a0001c0001t0001g0250 | 2 | HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-8+14570_-8+14571i others(598): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869593 | ||||||
chr7:148869593
|
C | CGCTCAAA others(1184): Show |
1 | a0001c0001t0001g0184 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-8+14570_-8+14571i others(1193): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869593 | ||||||
chr7:148869687
|
T | C | 3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0007t0001g0376 | 3 | HG02647.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+14477A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869687 | ||||||
chr7:148869751
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-8+14413A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869751 | ||||||
chr7:148869917
|
T | C | 1 | a0001c0001t0001g0332 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-8+14247A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869917 | ||||||
chr7:148869960
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0190a0001c0001t0001g0193others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+14204G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869960 | ||||||
chr7:148869980
|
G | A | 2 | a0002c0002t0001g0333a0002c0002t0001g0343 | 2 | HG00673.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-8+14184C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148869980 | ||||||
chr7:148870012
|
C | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | HG02970.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-8+14152G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148870012 | ||||||
chr7:148870024
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0190a0001c0001t0001g0193others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+14140G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148870024 | ||||||
chr7:148870171
|
C | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(276): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-8+13993G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148870171 | ||||||
chr7:148870349
|
C | G | 2 | a0001c0003t0001g0083a0001c0003t0001g0084 | 2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+13815G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148870349 | ||||||
chr7:148870405
|
A | G | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8+13759T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148870405 | ||||||
chr7:148870452
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+13712G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148870452 | ||||||
chr7:148870511
|
G | A | 5 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0164others(2): Show | 5 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+13653C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148870511 | ||||||
chr7:148870522
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(4): Show | 7 | HG00738.hp1 HG01175.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+13642G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148870522 | ||||||
chr7:148870672
|
G | A | 5 | a0001c0001t0002g0266a0001c0001t0002g0270a0001c0001t0002g0271others(2): Show | 5 | NA18951.hp1 NA18993.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+13492C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148870672 | ||||||
chr7:148870695
|
C | CA | 8 | a0001c0001t0001g0020a0001c0001t0001g0069a0001c0001t0001g0096others(5): Show | 8 | HG01891.hp2 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8+13468dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148870695 | ||||||
chr7:148870755
|
C | A | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8+13409G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148870755 | ||||||
chr7:148870764
|
T | C | 1 | a0001c0001t0001g0361 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-8+13400A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148870764 | ||||||
chr7:148870846
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-8+13318A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148870846 | ||||||
chr7:148870865
|
G | A | 81 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-8+13299C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148870865 | ||||||
chr7:148871142
|
T | C | 3 | a0001c0001t0001g0317a0001c0001t0001g0335a0001c0001t0001g0336 | 3 | HG00735.hp1 HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-8+13022A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871142 | ||||||
chr7:148871368
|
A | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-8+12796T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871368 | ||||||
chr7:148871403
|
T | TA | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(136): Show | 140 | HG00140.hp1 HG00621.hp2 HG00642.hp1 others(137): Show |
intron_variant | MODIFIER | c.-8+12760dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871403 | ||||||
chr7:148871403
|
T | TAA | 24 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0096others(21): Show | 25 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8+12759_-8+12760d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871403 | ||||||
chr7:148871403
|
TA | T | 82 | a0001c0001t0001g0047a0001c0001t0001g0294a0001c0001t0001g0296others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.-8+12760delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871403 | ||||||
chr7:148871403
|
TAA | T | 10 | a0001c0001t0001g0295a0001c0001t0001g0316a0001c0001t0001g0317others(7): Show | 10 | HG01257.hp2 HG01516.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+12759_-8+12760d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871403 | ||||||
chr7:148871403
|
TAAAAAAA others(1): Show |
T | 7 | a0001c0001t0001g0040a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02055.hp2 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+12753_-8+12760d others(10): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871403 | ||||||
chr7:148871423
|
A | G | 1 | a0001c0001t0001g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-8+12741T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871423 | ||||||
chr7:148871490
|
C | T | 1 | a0001c0001t0001g0314 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-8+12674G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871490 | ||||||
chr7:148871577
|
C | CT | 89 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(86): Show | 89 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.-8+12586dupA | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871577 | ||||||
chr7:148871577
|
C | CTTTTTTT others(9): Show |
3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0007t0001g0376 | 3 | HG02647.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+12586_-8+12587i others(18): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871577 | ||||||
chr7:148871589
|
T | C | 1 | a0001c0001t0002g0189 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-8+12575A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871589 | ||||||
chr7:148871720
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(4): Show | 7 | HG00738.hp1 HG01175.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+12444C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871720 | ||||||
chr7:148871723
|
T | C | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8+12441A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871723 | ||||||
chr7:148871795
|
G | A | 1 | a0001c0001t0001g0364 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-8+12369C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871795 | ||||||
chr7:148871873
|
C | A | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8+12291G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148871873 | ||||||
chr7:148872155
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(4): Show | 7 | HG00738.hp1 HG01175.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+12009C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148872155 | ||||||
chr7:148872352
|
A | C | 1 | a0001c0001t0002g0286 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-8+11812T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148872352 | ||||||
chr7:148872459
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-8+11705T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148872459 | ||||||
chr7:148872463
|
TA | T | 11 | a0001c0001t0002g0204a0001c0001t0002g0229a0001c0001t0002g0230others(8): Show | 11 | HG02040.hp1 NA18960.hp2 NA18961.hp1 others(8): Show |
intron_variant | MODIFIER | c.-8+11700delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148872463 | ||||||
chr7:148872525
|
A | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+11639T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148872525 | ||||||
chr7:148872570
|
G | C | 10 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(7): Show | 10 | HG01243.hp2 HG02809.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+11594C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148872570 | ||||||
chr7:148872596
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-8+11568A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148872596 | ||||||
chr7:148872598
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0190a0001c0001t0001g0193others(1): Show | 4 | HG01884.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+11566A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148872598 | ||||||
chr7:148872662
|
A | G | 1 | a0002c0002t0007g0378 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-8+11502T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148872662 | ||||||
chr7:148872765
|
G | A | 1 | a0002c0002t0001g0362 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-8+11399C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148872765 | ||||||
chr7:148872801
|
A | C | 7 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0091others(4): Show | 7 | HG01433.hp1 HG01952.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+11363T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148872801 | ||||||
chr7:148872867
|
T | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0020others(26): Show | 31 | HG00140.hp1 HG00639.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.-8+11297A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148872867 | ||||||
chr7:148872975
|
A | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+11189T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148872975 | ||||||
chr7:148872995
|
T | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0046others(27): Show | 30 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.-8+11169A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148872995 | ||||||
chr7:148873188
|
G | A | 84 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+10976C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873188 | ||||||
chr7:148873216
|
G | C | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-8+10948C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873216 | ||||||
chr7:148873252
|
A | G | 84 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+10912T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873252 | ||||||
chr7:148873290
|
A | G | 84 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+10874T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873290 | ||||||
chr7:148873352
|
C | T | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+10812G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873352 | ||||||
chr7:148873355
|
A | G | 81 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-8+10809T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873355 | ||||||
chr7:148873447
|
C | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.-8+10717G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873447 | ||||||
chr7:148873459
|
G | T | 84 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+10705C>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873459 | ||||||
chr7:148873483
|
C | T | 13 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(10): Show | 13 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8+10681G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873483 | ||||||
chr7:148873491
|
C | CA | 60 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(57): Show | 60 | HG00544.hp2 HG01081.hp2 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.-8+10672dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873491 | ||||||
chr7:148873491
|
C | CAAAAAA | 59 | a0001c0001t0001g0294a0001c0001t0001g0298a0001c0001t0001g0299others(56): Show | 59 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.-8+10667_-8+10672d others(8): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873491 | ||||||
chr7:148873491
|
C | CAAAAAAA | 19 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0306others(16): Show | 19 | HG00140.hp2 HG00597.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8+10666_-8+10672d others(9): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873491 | ||||||
chr7:148873491
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0158 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-8+10663_-8+10672d others(12): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873491 | ||||||
chr7:148873507
|
A | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(6): Show | 9 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+10657T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873507 | ||||||
chr7:148873554
|
T | A | 7 | a0001c0001t0002g0009a0001c0001t0002g0256a0001c0001t0002g0257others(4): Show | 7 | HG00741.hp1 HG01081.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+10610A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873554 | ||||||
chr7:148873555
|
TC | T | 3 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0258 | 3 | HG00741.hp1 HG01192.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-8+10608delG | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873555 | ||||||
chr7:148873555
|
TCA | T | 4 | a0001c0001t0002g0009a0001c0001t0002g0259a0001c0001t0002g0260others(1): Show | 4 | HG01081.hp1 HG02280.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+10607_-8+10608d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873555 | ||||||
chr7:148873557
|
A | AT | 79 | a0001c0001t0001g0020a0001c0001t0001g0040a0001c0001t0001g0044others(76): Show | 79 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-8+10606dupA | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873557 | ||||||
chr7:148873557
|
A | ATT | 15 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0001g0091others(12): Show | 15 | HG00544.hp2 HG01433.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-8+10605_-8+10606d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873557 | ||||||
chr7:148873557
|
A | T | 3 | a0001c0001t0002g0256a0001c0001t0002g0257a0001c0001t0002g0258 | 3 | HG00741.hp1 HG01192.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-8+10607T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873557 | ||||||
chr7:148873557
|
AT | A | 23 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(20): Show | 23 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.-8+10606delA | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873557 | ||||||
chr7:148873557
|
ATTTT | A | 9 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(6): Show | 9 | HG00639.hp2 HG00738.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+10603_-8+10606d others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873557 | ||||||
chr7:148873557
|
ATTTTT | A | 8 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+10602_-8+10606d others(7): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873557 | ||||||
chr7:148873557
|
ATTTTTTT | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0352others(13): Show | 16 | HG01074.hp2 HG01123.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8+10600_-8+10606d others(9): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873557 | ||||||
chr7:148873557
|
ATTTTTTT others(3): Show |
A | 1 | a0002c0002t0001g0300 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-8+10597_-8+10606d others(12): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873557 | ||||||
chr7:148873586
|
CAG | C | 13 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026others(10): Show | 13 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8+10576_-8+10577d others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873586 | ||||||
chr7:148873649
|
C | T | 95 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(92): Show | 95 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-8+10515G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873649 | ||||||
chr7:148873748
|
TC | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG02647.hp2 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+10415delG | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873748 | ||||||
chr7:148873790
|
T | C | 1 | a0001c0001t0002g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-8+10374A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873790 | ||||||
chr7:148873866
|
A | AG | 314 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(311): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.-8+10297_-8+10298i others(3): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873866 | ||||||
chr7:148873868
|
A | C | 314 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(311): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.-8+10296T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873868 | ||||||
chr7:148873885
|
T | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(142): Show | 147 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.-8+10279A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873885 | ||||||
chr7:148873989
|
A | C | 11 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+10175T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873989 | ||||||
chr7:148873996
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-8+10168A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148873996 | ||||||
chr7:148874030
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0193 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-8+10134C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148874030 | ||||||
chr7:148874104
|
G | A | 84 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(81): Show | 84 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-8+10060C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148874104 | ||||||
chr7:148874130
|
A | AT | 81 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-8+10033_-8+10034i others(3): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148874130 | ||||||
chr7:148874148
|
G | C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8+10016C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148874148 | ||||||
chr7:148874165
|
C | T | 3 | a0001c0003t0001g0083a0001c0003t0001g0084a0001c0007t0001g0376 | 3 | HG02647.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-8+9999G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148874165 | ||||||
chr7:148874205
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-8+9959T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148874205 | ||||||
chr7:148874280
|
C | G | 1 | a0001c0001t0001g0367 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-8+9884G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148874280 | ||||||
chr7:148874301
|
T | C | 80 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-8+9863A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148874301 | ||||||
chr7:148874382
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-8+9782G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148874382 | ||||||
chr7:148874416
|
C | A | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8+9748G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148874416 | ||||||
chr7:148874860
|
G | A | 5 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 5 | HG02083.hp1 NA18965.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+9304C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148874860 | ||||||
chr7:148874896
|
C | CA | 22 | a0001c0001t0001g0082a0001c0001t0001g0140a0001c0001t0001g0141others(19): Show | 22 | HG02040.hp1 HG02080.hp2 HG02647.hp1 others(19): Show |
intron_variant | MODIFIER | c.-8+9267dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148874896 | ||||||
chr7:148874896
|
CA | C | 18 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0047others(15): Show | 18 | HG01168.hp2 HG01169.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8+9267delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148874896 | ||||||
chr7:148874971
|
C | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0025a0001c0001t0001g0026 | 3 | HG00738.hp1 HG01175.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-8+9193G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148874971 | ||||||
chr7:148875135
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-8+9029T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148875135 | ||||||
chr7:148875412
|
G | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(273): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-8+8752C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148875412 | ||||||
chr7:148875421
|
CCAGA | C | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(1): Show | 4 | HG02615.hp2 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+8739_-8+8742del others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148875421 | ||||||
chr7:148875438
|
T | C | 1 | a0001c0001t0002g0238 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-8+8726A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148875438 | ||||||
chr7:148875594
|
A | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+8570T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148875594 | ||||||
chr7:148875598
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-8+8566C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148875598 | ||||||
chr7:148875864
|
A | T | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8+8300T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148875864 | ||||||
chr7:148875935
|
C | A | 80 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(77): Show | 80 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-8+8229G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148875935 | ||||||
chr7:148875969
|
G | A | 81 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-8+8195C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148875969 | ||||||
chr7:148876023
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-8+8141C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148876023 | ||||||
chr7:148876182
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-8+7982C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148876182 | ||||||
chr7:148876183
|
A | G | 1 | a0001c0001t0001g0022 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-8+7981T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148876183 | ||||||
chr7:148876219
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(162): Show | 167 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(164): Show |
intron_variant | MODIFIER | c.-8+7945C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148876219 | ||||||
chr7:148876228
|
A | G | 20 | a0001c0001t0001g0022a0001c0001t0001g0065a0001c0001t0001g0066others(17): Show | 20 | HG00597.hp2 HG02071.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.-8+7936T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148876228 | ||||||
chr7:148876232
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-8+7932T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148876232 | ||||||
chr7:148876256
|
C | T | 4 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(1): Show | 4 | HG00639.hp2 HG00738.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+7908G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148876256 | ||||||
chr7:148876292
|
G | GA | 81 | a0001c0001t0001g0158a0001c0001t0001g0294a0001c0001t0001g0295others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.-8+7871dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148876292 | ||||||
chr7:148876535
|
T | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-8+7629A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148876535 | ||||||
chr7:148876600
|
CTTCTT | C | 78 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(75): Show | 78 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-8+7559_-8+7563del others(5): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148876600 | ||||||
chr7:148876650
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-8+7514G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148876650 | ||||||
chr7:148876684
|
C | T | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8+7480G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148876684 | ||||||
chr7:148876806
|
G | A | 81 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-8+7358C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148876806 | ||||||
chr7:148876860
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8+7304C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148876860 | ||||||
chr7:148877189
|
T | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8+6975A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148877189 | ||||||
chr7:148877272
|
A | C | 1 | a0001c0009t0001g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-8+6892T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148877272 | ||||||
chr7:148877376
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-8+6788G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148877376 | ||||||
chr7:148877855
|
A | G | 1 | a0002c0002t0001g0297 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-8+6309T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148877855 | ||||||
chr7:148878095
|
T | G | 1 | a0001c0001t0001g0255 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-8+6069A>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148878095 | ||||||
chr7:148878243
|
CTCTGTAT others(8): Show |
C | 1 | a0001c0001t0002g0010 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-8+5906_-8+5920del others(15): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148878243 | ||||||
chr7:148878291
|
T | C | 2 | a0001c0001t0002g0239a0001c0001t0002g0240 | 2 | NA19003.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-8+5873A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148878291 | ||||||
chr7:148878322
|
G | A | 26 | a0001c0001t0001g0046a0001c0001t0001g0143a0001c0001t0001g0144others(23): Show | 26 | HG00280.hp2 HG01070.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8+5842C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148878322 | ||||||
chr7:148878353
|
G | C | 1 | a0001c0001t0001g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+5811C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148878353 | ||||||
chr7:148878424
|
C | G | 2 | a0001c0003t0001g0377a0001c0007t0001g0376 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-8+5740G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148878424 | ||||||
chr7:148878716
|
T | C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8+5448A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148878716 | ||||||
chr7:148878728
|
G | A | 7 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(4): Show | 7 | HG00280.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+5436C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148878728 | ||||||
chr7:148878855
|
C | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(276): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-8+5309G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148878855 | ||||||
chr7:148878890
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-8+5274G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148878890 | ||||||
chr7:148878945
|
G | A | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8+5219C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148878945 | ||||||
chr7:148878950
|
C | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.-8+5214G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148878950 | ||||||
chr7:148879017
|
C | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(283): Show | 288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.-8+5147G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879017 | ||||||
chr7:148879041
|
G | A | 1 | a0001c0001t0001g0364 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-8+5123C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879041 | ||||||
chr7:148879101
|
C | T | 88 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(85): Show | 88 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-8+5063G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879101 | ||||||
chr7:148879174
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-8+4990C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879174 | ||||||
chr7:148879200
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-8+4964C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879200 | ||||||
chr7:148879224
|
TCAAAAAA others(12): Show |
T | 10 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(7): Show | 10 | HG01243.hp2 HG02809.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+4921_-8+4939del others(19): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879224 | ||||||
chr7:148879226
|
A | AAAAAAC | 5 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+4932_-8+4937dup others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879226 | ||||||
chr7:148879274
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-8+4890C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879274 | ||||||
chr7:148879405
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-8+4759G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879405 | ||||||
chr7:148879406
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-8+4758C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879406 | ||||||
chr7:148879534
|
T | C | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | NA18953.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.-8+4630A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879534 | ||||||
chr7:148879578
|
C | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0365 | 2 | HG01257.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-8+4586G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879578 | ||||||
chr7:148879805
|
C | CA | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(4): Show | 7 | HG02257.hp2 HG02451.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+4358dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879805 | ||||||
chr7:148879812
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02155.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-8+4352T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879812 | ||||||
chr7:148879859
|
C | A | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8+4305G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879859 | ||||||
chr7:148879928
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-8+4236C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879928 | ||||||
chr7:148879941
|
CA | C | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8+4222delT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148879941 | ||||||
chr7:148880518
|
C | G | 81 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.-8+3646G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148880518 | ||||||
chr7:148880596
|
T | A | 1 | a0001c0001t0001g0170 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-8+3568A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148880596 | ||||||
chr7:148880872
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-8+3292A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148880872 | ||||||
chr7:148880874
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-8+3290T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148880874 | ||||||
chr7:148881046
|
G | C | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174 | 3 | HG01978.hp2 HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-8+3118C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881046 | ||||||
chr7:148881119
|
T | C | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8+3045A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881119 | ||||||
chr7:148881206
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-8+2958A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881206 | ||||||
chr7:148881220
|
T | A | 1 | a0001c0001t0001g0022 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-8+2944A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881220 | ||||||
chr7:148881236
|
T | A | 1 | a0001c0001t0001g0022 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-8+2928A>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881236 | ||||||
chr7:148881387
|
T | C | 5 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(2): Show | 5 | HG02280.hp2 HG02647.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+2777A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881387 | ||||||
chr7:148881451
|
C | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-8+2713G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881451 | ||||||
chr7:148881661
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(162): Show | 167 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(164): Show |
intron_variant | MODIFIER | c.-8+2503C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881661 | ||||||
chr7:148881731
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG00741.hp2 HG01978.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-8+2433G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881731 | ||||||
chr7:148881797
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-8+2367G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881797 | ||||||
chr7:148881933
|
C | CA | 86 | a0001c0001t0001g0039a0001c0001t0001g0175a0001c0001t0001g0294others(83): Show | 86 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.-8+2230dupT | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881933 | ||||||
chr7:148881940
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-8+2224T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881940 | ||||||
chr7:148881951
|
T | C | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8+2213A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881951 | ||||||
chr7:148881964
|
A | G | 8 | a0001c0001t0001g0025a0001c0001t0002g0009a0001c0001t0002g0256others(5): Show | 8 | HG00741.hp1 HG01081.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+2200T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881964 | ||||||
chr7:148881964
|
ACG | A | 8 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+2198_-8+2199del others(2): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881964 | ||||||
chr7:148881968
|
GCGCGCAC others(3): Show |
G | 5 | a0001c0001t0001g0366a0001c0001t0001g0367a0001c0001t0001g0368others(2): Show | 5 | HG00140.hp2 HG02015.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+2186_-8+2195del others(10): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881968 | ||||||
chr7:148881968
|
GCGCGCAC others(5): Show |
G | 75 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(72): Show | 75 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8+2184_-8+2195del others(12): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881968 | ||||||
chr7:148881972
|
G | A | 7 | a0001c0001t0002g0009a0001c0001t0002g0256a0001c0001t0002g0257others(4): Show | 7 | HG00741.hp1 HG01081.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+2192C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881972 | ||||||
chr7:148881972
|
G | GCA | 26 | a0001c0001t0002g0010a0001c0001t0002g0262a0001c0001t0002g0263others(23): Show | 26 | HG01243.hp1 HG01515.hp2 HG01516.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8+2190_-8+2191dup others(2): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881972 | ||||||
chr7:148881972
|
G | GCACA | 5 | a0001c0001t0001g0289a0001c0001t0002g0286a0001c0001t0002g0287others(2): Show | 5 | HG00544.hp2 HG02451.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+2188_-8+2191dup others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881972 | ||||||
chr7:148881972
|
GCA | G | 23 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(20): Show | 23 | HG01167.hp1 HG01884.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.-8+2190_-8+2191del others(2): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881972 | ||||||
chr7:148881972
|
GCACA | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(147): Show | 152 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(149): Show |
intron_variant | MODIFIER | c.-8+2188_-8+2191del others(4): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881972 | ||||||
chr7:148881972
|
GCACACA | G | 13 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(10): Show | 13 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8+2186_-8+2191del others(6): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881972 | ||||||
chr7:148881974
|
A | G | 7 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0002g0178others(4): Show | 7 | HG00639.hp2 HG00738.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+2190T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881974 | ||||||
chr7:148881976
|
A | G | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+2188T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881976 | ||||||
chr7:148881978
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0027 | 3 | HG00738.hp1 HG04184.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-8+2186T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881978 | ||||||
chr7:148881980
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0024 | 2 | HG01952.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-8+2184T>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881980 | ||||||
chr7:148881981
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-8+2183G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881981 | ||||||
chr7:148881997
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-8+2167G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148881997 | ||||||
chr7:148882001
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-8+2163A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148882001 | ||||||
chr7:148882002
|
A | T | 1 | a0001c0001t0001g0022 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-8+2162T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148882002 | ||||||
chr7:148882020
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02257.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-8+2144C>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148882020 | ||||||
chr7:148882021
|
A | C | 3 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0003t0001g0377 | 3 | HG02109.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-8+2143T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148882021 | ||||||
chr7:148882356
|
A | T | 1 | a0001c0001t0001g0021 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-8+1808T>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148882356 | ||||||
chr7:148882407
|
A | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+1757T>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148882407 | ||||||
chr7:148882436
|
GAAC | G | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+1725_-8+1727del others(3): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148882436 | ||||||
chr7:148883094
|
G | C | 1 | a0001c0003t0001g0377 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8+1070C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883094 | ||||||
chr7:148883189
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-8+975G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883189 | ||||||
chr7:148883193
|
T | C | 1 | a0001c0001t0001g0375 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-8+971A>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883193 | ||||||
chr7:148883205
|
C | G | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+959G>C | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883205 | ||||||
chr7:148883334
|
C | T | 1 | a0001c0007t0001g0376 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8+830G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883334 | ||||||
chr7:148883356
|
C | CAGAGCAG others(4): Show |
1 | a0001c0001t0002g0010 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-8+797_-8+807dupCG others(9): Show |
EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883356 | ||||||
chr7:148883397
|
G | C | 1 | a0001c0001t0001g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8+767C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883397 | ||||||
chr7:148883555
|
G | C | 1 | a0001c0001t0002g0293 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-8+609C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883555 | ||||||
chr7:148883705
|
G | T | 1 | a0001c0001t0002g0009 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-8+459C>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883705 | ||||||
chr7:148883717
|
G | C | 82 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0294others(79): Show | 82 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.-8+447C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883717 | ||||||
chr7:148883756
|
C | A | 1 | a0001c0001t0002g0373 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-8+408G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883756 | ||||||
chr7:148883812
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-8+352G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883812 | ||||||
chr7:148883814
|
C | A | 2 | a0001c0001t0001g0374a0001c0001t0001g0375 | 2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-8+350G>T | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883814 | ||||||
chr7:148883891
|
C | T | 2 | a0001c0001t0002g0006a0001c0001t0002g0007 | 2 | NA18959.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-8+273G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883891 | ||||||
chr7:148883922
|
G | C | 2 | a0001c0003t0001g0377a0001c0007t0001g0376 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-8+242C>G | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883922 | ||||||
chr7:148883978
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01074.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-8+186G>A | EZH2 | ENSG00000106462.12 | transcript | ENST00000320356.7 | protein_coding | 1/19 | chr7 | 148883978 |