geneid | 8726 |
---|---|
ensemblid | ENSG00000074266.23 |
hgncid | 3188 |
symbol | EED |
name | embryonic ectoderm development |
refseq_nuc | NM_003797.5 |
refseq_prot | NP_003788.2 |
ensembl_nuc | ENST00000263360.11 |
ensembl_prot | ENSP00000263360.6 |
mane_status | MANE Select |
chr | chr11 |
start | 86244753 |
end | 86278810 |
strand | + |
ver | v1.2 |
region | chr11:86244753-86278810 |
region5000 | chr11:86239753-86283810 |
regionname0 | EED_chr11_86244753_86278810 |
regionname5000 | EED_chr11_86239753_86283810 |
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 | 441 | 391 | 84 | 60 | 189 | 14 | 42 | 149 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
a0002 | 0/0 | 441 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
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 | 1/0 | 1326 | 274 | 72 | 41 | 126 | 8 | 26 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
c0002 | 0/1 | 1326 | 116 | 12 | 19 | 62 | 6 | 16 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
c0003 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
c0004 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 763 | 385 | 81 | 59 | 188 | 14 | 41 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
t0002 | 0/0 | 763 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
t0003 | 0/0 | 763 | 2 | 0 | 1 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
t0004 | 0/0 | 763 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
t0005 | 0/0 | 763 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
t0006 | 0/0 | 763 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
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 | 11 | 0 | 1 | 5 | 1 | 4 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0002 | 0/0 | 9 | 0 | 5 | 1 | 1 | 2 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0003 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0005 | 0/0 | 5 | 2 | 0 | 1 | 0 | 2 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0008 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0017 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0018 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0021 | 0/1 | 3 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0038 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0043 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
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 | 1/0 | 1326 | 274 | 72 | 41 | 126 | 8 | 26 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
a0001c0002 | 0/1 | 1326 | 116 | 12 | 19 | 62 | 6 | 16 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
a0001c0003 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
a0002c0004 | 0/0 | 1326 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2088 | 267 | 69 | 40 | 124 | 8 | 25 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
a0001c0001t0002 | 0/0 | 2088 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
a0001c0001t0003 | 0/0 | 2088 | 2 | 0 | 1 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
a0001c0001t0004 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
a0001c0001t0005 | 0/0 | 2088 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
a0001c0001t0006 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
a0001c0002t0001 | 0/1 | 2088 | 116 | 12 | 19 | 62 | 6 | 16 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
a0001c0003t0001 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
a0002c0004t0001 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | copy fasta | chr11 | 86239753 | 86283810 |
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 | 11 | 0 | 1 | 5 | 1 | 4 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0008 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0017 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0018 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0067 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0002 | 0/0 | 9 | 0 | 5 | 1 | 1 | 2 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0005 | 0/0 | 5 | 2 | 0 | 1 | 0 | 2 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0021 | 0/1 | 3 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0038 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0001c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
a0002c0004t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | FIN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | FIN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00423 | hp1 | a0001 | c0003 | t0001 | g0016 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0244 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0277 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0271 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0276 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0245 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0046 | EUR | IBS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0046 | EUR | IBS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0242 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0265 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | CDX | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0255 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0261 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0041 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0289 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0041 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0295 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0164 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0231 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0201 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0270 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0178 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0248 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0243 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0176 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0264 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0263 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0249 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0241 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0262 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0173 | SAS | STU | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | CHB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | LWK | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19054 | hp2 | a0002 | c0004 | t0001 | g0014 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19075 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | ASW | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ASW | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0266 | EUR | TSI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0269 | EUR | TSI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0170 | EUR | TSI | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | GIH | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | CLM | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | USA | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | USA | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0021 | REF | REF | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0067 | REF | REF | EED_chr11_86239753_86283810 | EED | chr11 | 86239753 | 86283810 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:86245285
|
A | G | 1 | a0002 | 1 | NA19054.hp2 | missense_variant | MODERATE | c.56A>G | p.Lys19Arg | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/12 | 533/2088 | 56/1326 | 19/441 | chr11 | 86245285 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:86257581
|
C | T | 1 | a0001c0002 | 116 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(113): Show |
synonymous_variant | LOW | c.619C>T | p.Leu207Leu | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/12 | 1096/2088 | 619/1326 | 207/441 | chr11 | 86257581 | ||
chr11:86277015
|
C | A | 1 | a0001c0003 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.1002C>A | p.Gly334Gly | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 10/12 | 1479/2088 | 1002/1326 | 334/441 | chr11 | 86277015 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:86244810
|
G | C | 1 | a0001c0001t0004 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-420G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/12 | 420 | chr11 | 86244810 | |||||
chr11:86244987
|
G | A | 1 | a0001c0001t0005 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-243G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/12 | 243 | chr11 | 86244987 | |||||
chr11:86245106
|
G | T | 1 | a0001c0001t0003 | 2 | HG01934.hp1 NA18957.hp1 |
5_prime_UTR_variant | MODIFIER | c.-124G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/12 | 124 | chr11 | 86245106 | |||||
chr11:86245204
|
A | C | 1 | a0001c0001t0006 | 1 | HG02083.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/12 | 26 | chr11 | 86245204 | |||||
chr11:86245208
|
A | T | 1 | a0001c0001t0002 | 2 | HG02886.hp1 HG03209.hp1 |
5_prime_UTR_variant | MODIFIER | c.-22A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/12 | 22 | chr11 | 86245208 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:86245361
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0296 | 5 | HG00408.hp1 HG00609.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+18C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86245361 | ||||||
chr11:86245434
|
G | T | 2 | a0001c0001t0002g0294a0001c0001t0002g0295 | 2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.114+91G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86245434 | ||||||
chr11:86245436
|
G | T | 13 | a0001c0001t0001g0048a0001c0001t0001g0282a0001c0001t0001g0283others(10): Show | 14 | HG00323.hp1 HG00639.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.114+93G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86245436 | ||||||
chr11:86245448
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.114+105G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86245448 | ||||||
chr11:86245579
|
C | G | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | NA18948.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.114+236C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86245579 | ||||||
chr11:86246007
|
G | T | 1 | a0001c0001t0001g0279 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.114+664G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246007 | ||||||
chr11:86246243
|
T | TAACC | 2 | a0001c0001t0001g0022a0001c0001t0001g0050 | 3 | HG03195.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.114+902_114+905dup others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 86246243 | |||||
chr11:86246272
|
C | G | 43 | a0001c0002t0001g0002a0001c0002t0001g0020a0001c0002t0001g0021others(40): Show | 57 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.114+929C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246272 | ||||||
chr11:86246274
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0042others(53): Show | 72 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.114+931A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246274 | ||||||
chr11:86246416
|
A | G | 39 | a0001c0001t0001g0207a0001c0002t0001g0002a0001c0002t0001g0020others(36): Show | 53 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.114+1073A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246416 | ||||||
chr11:86246649
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0042others(53): Show | 72 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.114+1306A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246649 | ||||||
chr11:86246703
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(201): Show | 259 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.114+1360A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246703 | ||||||
chr11:86246725
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.114+1382C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246725 | ||||||
chr11:86246951
|
C | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 12 | HG00140.hp2 HG00280.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.114+1608C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246951 | ||||||
chr11:86246957
|
G | A | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.114+1614G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246957 | ||||||
chr11:86246988
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.114+1645A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86246988 | ||||||
chr11:86247107
|
A | C | 1 | a0001c0001t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.114+1764A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247107 | ||||||
chr11:86247121
|
A | G | 1 | a0001c0001t0001g0032 | 2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.114+1778A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247121 | ||||||
chr11:86247345
|
A | T | 119 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(116): Show | 152 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.114+2002A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247345 | ||||||
chr11:86247421
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.114+2078G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247421 | ||||||
chr11:86247428
|
A | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.114+2085A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247428 | ||||||
chr11:86247500
|
G | A | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.114+2157G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247500 | ||||||
chr11:86247605
|
G | C | 1 | a0001c0001t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.114+2262G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247605 | ||||||
chr11:86247718
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(103): Show | 131 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.114+2375T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86247718 | ||||||
chr11:86248001
|
A | G | 49 | a0001c0002t0001g0005a0001c0002t0001g0010a0001c0002t0001g0019others(46): Show | 62 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.115-2295A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248001 | ||||||
chr11:86248119
|
T | G | 3 | a0001c0002t0001g0246a0001c0002t0001g0247a0001c0002t0001g0248 | 3 | HG01106.hp1 HG01978.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.115-2177T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248119 | ||||||
chr11:86248200
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0050 | 3 | HG03195.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.115-2096A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248200 | ||||||
chr11:86248284
|
A | G | 15 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0109others(12): Show | 19 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.115-2012A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248284 | ||||||
chr11:86248309
|
G | A | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.115-1987G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248309 | ||||||
chr11:86248322
|
G | C | 119 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(116): Show | 152 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.115-1974G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248322 | ||||||
chr11:86248429
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(196): Show | 251 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.115-1867C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248429 | ||||||
chr11:86248628
|
G | C | 119 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(116): Show | 152 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.115-1668G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248628 | ||||||
chr11:86248741
|
G | GGGCGCA | 27 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.115-1553_115-1548d others(8): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 86248741 | |||||
chr11:86248766
|
C | A | 1 | a0001c0001t0001g0052 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.115-1530C>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248766 | ||||||
chr11:86248789
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0031others(76): Show | 98 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-1507T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86248789 | ||||||
chr11:86249162
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0042others(53): Show | 72 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.115-1134A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86249162 | ||||||
chr11:86249298
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.115-998A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86249298 | ||||||
chr11:86249347
|
A | C | 1 | a0001c0001t0001g0162 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.115-949A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86249347 | ||||||
chr11:86249381
|
G | GA | 102 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(99): Show | 127 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.115-898dupA | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 86249381 | |||||
chr11:86249381
|
G | GAA | 6 | a0001c0001t0001g0053a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 6 | HG01069.hp2 HG02572.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-899_115-898dup others(2): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr11 | 86249381 | |||||
chr11:86249615
|
G | T | 1 | a0001c0002t0001g0202 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.115-681G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86249615 | ||||||
chr11:86249680
|
CAAT | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0031others(76): Show | 98 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-615_115-613del others(3): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86249680 | ||||||
chr11:86249750
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.115-546G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86249750 | ||||||
chr11:86249847
|
C | A | 9 | a0001c0001t0001g0031a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 10 | HG02572.hp1 HG02809.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-449C>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86249847 | ||||||
chr11:86250124
|
C | T | 92 | a0001c0001t0001g0165a0001c0001t0001g0203a0001c0001t0001g0204others(89): Show | 119 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.115-172C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 1/11 | chr11 | 86250124 | ||||||
chr11:86250563
|
A | G | 4 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(1): Show | 4 | HG02976.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+115A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86250563 | ||||||
chr11:86250578
|
GT | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0031others(75): Show | 97 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.267+141delT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr11 | 86250578 | |||||
chr11:86250604
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0031others(76): Show | 98 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.267+156G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86250604 | ||||||
chr11:86250702
|
T | G | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.267+254T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86250702 | ||||||
chr11:86250721
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.267+273A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86250721 | ||||||
chr11:86250728
|
G | T | 4 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(1): Show | 4 | HG02976.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+280G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86250728 | ||||||
chr11:86250831
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.267+383G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86250831 | ||||||
chr11:86250955
|
G | A | 5 | a0001c0001t0001g0033a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 6 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.267+507G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86250955 | ||||||
chr11:86251252
|
T | C | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+804T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86251252 | ||||||
chr11:86251311
|
G | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0042others(53): Show | 72 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.268-837G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86251311 | ||||||
chr11:86251339
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.268-809C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86251339 | ||||||
chr11:86251516
|
T | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(221): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.268-632T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86251516 | ||||||
chr11:86251905
|
G | A | 23 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(20): Show | 37 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.268-243G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86251905 | ||||||
chr11:86251959
|
C | T | 27 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.268-189C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86251959 | ||||||
chr11:86252105
|
G | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.268-43G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 2/11 | chr11 | 86252105 | ||||||
chr11:86252510
|
C | CA | 6 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 13 | HG00140.hp2 HG00280.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+270_360+271ins others(1): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252510 | ||||||
chr11:86252511
|
G | GC | 45 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0032others(42): Show | 53 | HG00408.hp2 HG01074.hp2 HG01496.hp1 others(50): Show |
intron_variant | MODIFIER | c.360+271_360+272ins others(1): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252511 | ||||||
chr11:86252511
|
G | GT | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(179): Show | 240 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.360+272dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86252511 | |||||
chr11:86252511
|
G | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(3): Show | 13 | HG00140.hp2 HG00280.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+271G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252511 | ||||||
chr11:86252512
|
T | TTC | 60 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(57): Show | 80 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.360+272_360+273ins others(2): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252512 | ||||||
chr11:86252513
|
C | T | 5 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0107others(2): Show | 5 | HG01070.hp1 HG01168.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+273C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252513 | ||||||
chr11:86252514
|
C | CT | 42 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0034others(39): Show | 49 | HG00408.hp2 HG01074.hp2 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.360+289dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86252514 | |||||
chr11:86252514
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0022others(57): Show | 80 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.360+274C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252514 | ||||||
chr11:86252515
|
T | C | 4 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0107others(1): Show | 4 | HG01070.hp1 HG01168.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+275T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252515 | ||||||
chr11:86252577
|
C | T | 93 | a0001c0001t0001g0165a0001c0001t0001g0203a0001c0001t0001g0204others(90): Show | 120 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.360+337C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252577 | ||||||
chr11:86252590
|
T | C | 93 | a0001c0001t0001g0165a0001c0001t0001g0203a0001c0001t0001g0204others(90): Show | 120 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.360+350T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252590 | ||||||
chr11:86252744
|
A | ATTGTTG | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.360+522_360+527dup others(6): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86252744 | |||||
chr11:86252899
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.360+659A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86252899 | ||||||
chr11:86253045
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.360+805G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253045 | ||||||
chr11:86253386
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.360+1146T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253386 | ||||||
chr11:86253470
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0119 | 2 | NA18991.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.360+1230A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253470 | ||||||
chr11:86253585
|
C | T | 137 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0032others(134): Show | 172 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.360+1345C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253585 | ||||||
chr11:86253643
|
T | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0033others(58): Show | 78 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.360+1403T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253643 | ||||||
chr11:86253687
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.360+1447T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253687 | ||||||
chr11:86253768
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0161 | 3 | NA18953.hp1 NA18974.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.361-1454C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253768 | ||||||
chr11:86253845
|
C | T | 92 | a0001c0001t0001g0165a0001c0001t0001g0203a0001c0001t0001g0204others(89): Show | 119 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.361-1377C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253845 | ||||||
chr11:86253864
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.361-1358G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253864 | ||||||
chr11:86253903
|
C | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0033others(58): Show | 78 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.361-1319C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253903 | ||||||
chr11:86253934
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0033others(58): Show | 78 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.361-1288G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253934 | ||||||
chr11:86253940
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.361-1282C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86253940 | ||||||
chr11:86254040
|
C | T | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.361-1182C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254040 | ||||||
chr11:86254048
|
C | CA | 25 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0056others(22): Show | 25 | HG00738.hp1 HG01099.hp1 HG01978.hp1 others(22): Show |
intron_variant | MODIFIER | c.361-1147dupA | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | |||||
chr11:86254048
|
C | CAA | 7 | a0001c0001t0001g0070a0001c0001t0001g0165a0001c0001t0001g0203others(4): Show | 8 | HG01168.hp2 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.361-1148_361-1147d others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | |||||
chr11:86254048
|
C | CAAA | 16 | a0001c0002t0001g0002a0001c0002t0001g0021a0001c0002t0001g0046others(13): Show | 27 | HG00280.hp1 HG00741.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.361-1149_361-1147d others(5): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | |||||
chr11:86254048
|
C | CAAAA | 18 | a0001c0002t0001g0020a0001c0002t0001g0198a0001c0002t0001g0199others(15): Show | 20 | HG00738.hp2 HG01123.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.361-1150_361-1147d others(6): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | |||||
chr11:86254048
|
C | CAAAAA | 31 | a0001c0002t0001g0005a0001c0002t0001g0010a0001c0002t0001g0019others(28): Show | 41 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.361-1151_361-1147d others(7): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | |||||
chr11:86254048
|
C | CAAAAAA | 19 | a0001c0002t0001g0038a0001c0002t0001g0039a0001c0002t0001g0040others(16): Show | 22 | HG01106.hp1 HG01978.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.361-1152_361-1147d others(8): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | |||||
chr11:86254048
|
CA | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0031others(60): Show | 79 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.361-1147delA | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | |||||
chr11:86254048
|
CAAA | C | 21 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(18): Show | 27 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.361-1149_361-1147d others(5): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | |||||
chr11:86254048
|
CAAAAAAA others(9): Show |
C | 18 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 25 | HG00741.hp1 HG01192.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.361-1162_361-1147d others(18): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254048 | |||||
chr11:86254063
|
A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.361-1159A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254063 | ||||||
chr11:86254069
|
A | G | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.361-1153A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254069 | ||||||
chr11:86254105
|
G | A | 1 | a0001c0002t0001g0180 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.361-1117G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254105 | ||||||
chr11:86254237
|
T | C | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.361-985T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254237 | ||||||
chr11:86254323
|
G | GT | 33 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0052others(30): Show | 35 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.361-884dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | 86254323 | |||||
chr11:86254372
|
G | A | 1 | a0001c0002t0001g0266 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.361-850G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254372 | ||||||
chr11:86254385
|
A | G | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.361-837A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254385 | ||||||
chr11:86254403
|
T | G | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.361-819T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254403 | ||||||
chr11:86254541
|
G | C | 3 | a0001c0001t0001g0033a0001c0001t0001g0138a0001c0001t0001g0139 | 4 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-681G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254541 | ||||||
chr11:86254566
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.361-656G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254566 | ||||||
chr11:86254622
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.361-600T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254622 | ||||||
chr11:86254672
|
G | C | 1 | a0001c0002t0001g0267 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.361-550G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254672 | ||||||
chr11:86254708
|
C | T | 2 | a0001c0002t0001g0178a0001c0002t0001g0196 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.361-514C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254708 | ||||||
chr11:86254715
|
C | T | 1 | a0001c0001t0002g0294 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.361-507C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254715 | ||||||
chr11:86254764
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0089 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.361-458G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254764 | ||||||
chr11:86254766
|
GC | G | 18 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 25 | HG00741.hp1 HG01192.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.361-455delC | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254766 | ||||||
chr11:86254780
|
G | A | 1 | a0001c0002t0001g0181 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.361-442G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254780 | ||||||
chr11:86254867
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(197): Show | 252 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.361-355T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254867 | ||||||
chr11:86254882
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.361-340A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254882 | ||||||
chr11:86254896
|
C | T | 88 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0010others(85): Show | 115 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.361-326C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254896 | ||||||
chr11:86254911
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.361-311G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86254911 | ||||||
chr11:86255009
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.361-213G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86255009 | ||||||
chr11:86255135
|
G | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(196): Show | 251 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.361-87G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 3/11 | chr11 | 86255135 | ||||||
chr11:86255500
|
A | C | 92 | a0001c0001t0001g0165a0001c0001t0001g0203a0001c0001t0001g0204others(89): Show | 119 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.426+213A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255500 | ||||||
chr11:86255517
|
G | A | 1 | a0001c0002t0001g0196 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.426+230G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255517 | ||||||
chr11:86255518
|
A | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0033others(58): Show | 78 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.426+231A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255518 | ||||||
chr11:86255533
|
G | A | 92 | a0001c0001t0001g0165a0001c0001t0001g0203a0001c0001t0001g0204others(89): Show | 119 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.426+246G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255533 | ||||||
chr11:86255544
|
T | C | 88 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0010others(85): Show | 115 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.426+257T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255544 | ||||||
chr11:86255623
|
C | G | 92 | a0001c0001t0001g0165a0001c0001t0001g0203a0001c0001t0001g0204others(89): Show | 119 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.426+336C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255623 | ||||||
chr11:86255705
|
C | T | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.426+418C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255705 | ||||||
chr11:86255747
|
T | C | 1 | a0001c0002t0001g0200 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.426+460T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255747 | ||||||
chr11:86255873
|
G | T | 1 | a0001c0002t0001g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.427-514G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255873 | ||||||
chr11:86255908
|
C | G | 1 | a0001c0002t0001g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.427-479C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255908 | ||||||
chr11:86255918
|
T | TA | 3 | a0001c0002t0001g0253a0001c0002t0001g0254a0001c0002t0001g0268 | 3 | NA18952.hp1 NA18972.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.427-465dupA | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr11 | 86255918 | |||||
chr11:86255933
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.427-454T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86255933 | ||||||
chr11:86256022
|
A | G | 90 | a0001c0001t0001g0165a0001c0002t0001g0002a0001c0002t0001g0005others(87): Show | 117 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.427-365A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86256022 | ||||||
chr11:86256256
|
A | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0042others(53): Show | 72 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.427-131A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 4/11 | chr11 | 86256256 | ||||||
chr11:86256545
|
T | G | 1 | a0001c0002t0001g0169 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.552+33T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256545 | ||||||
chr11:86256604
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.552+92T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256604 | ||||||
chr11:86256610
|
A | C | 1 | a0001c0001t0001g0293 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.552+98A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256610 | ||||||
chr11:86256628
|
A | G | 4 | a0001c0001t0001g0085a0001c0002t0001g0261a0001c0002t0001g0266others(1): Show | 4 | HG01258.hp1 HG02273.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.552+116A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256628 | ||||||
chr11:86256667
|
G | A | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0010others(86): Show | 116 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.552+155G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256667 | ||||||
chr11:86256719
|
A | C | 1 | a0001c0001t0001g0293 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.552+207A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256719 | ||||||
chr11:86256900
|
G | A | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.552+388G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256900 | ||||||
chr11:86256910
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.552+398A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256910 | ||||||
chr11:86256995
|
C | T | 92 | a0001c0001t0001g0165a0001c0001t0001g0203a0001c0001t0001g0204others(89): Show | 119 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.552+483C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86256995 | ||||||
chr11:86257003
|
C | T | 1 | a0001c0001t0001g0029 | 2 | NA18612.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.552+491C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86257003 | ||||||
chr11:86257031
|
G | A | 1 | a0001c0002t0001g0269 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.553-484G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86257031 | ||||||
chr11:86257063
|
A | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(295): Show | 391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.553-452A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86257063 | ||||||
chr11:86257122
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.553-393G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86257122 | ||||||
chr11:86257185
|
T | TTG | 12 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0028others(9): Show | 16 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(13): Show |
intron_variant | MODIFIER | c.553-298_553-297dup others(2): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257185 | |||||
chr11:86257185
|
T | TTGTG | 3 | a0001c0001t0001g0130a0001c0001t0001g0205a0001c0001t0002g0294 | 3 | HG01891.hp2 HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.553-300_553-297dup others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257185 | |||||
chr11:86257185
|
T | TTGTGTGT others(1): Show |
14 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0122others(11): Show | 16 | HG01074.hp2 HG01884.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.553-304_553-297dup others(8): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257185 | |||||
chr11:86257185
|
T | TTGTGTGT others(3): Show |
3 | a0001c0001t0001g0049a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG02273.hp2 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.553-306_553-297dup others(10): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257185 | |||||
chr11:86257185
|
TTG | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0033others(125): Show | 172 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.553-298_553-297del others(2): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257185 | |||||
chr11:86257185
|
TTGTG | T | 14 | a0001c0001t0001g0165a0001c0001t0001g0203a0001c0001t0001g0204others(11): Show | 14 | HG01192.hp2 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.553-300_553-297del others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257185 | |||||
chr11:86257185
|
TTGTGTGT others(1): Show |
T | 26 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 32 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(29): Show |
intron_variant | MODIFIER | c.553-304_553-297del others(8): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257185 | |||||
chr11:86257323
|
C | T | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.553-192C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86257323 | ||||||
chr11:86257340
|
CT | C | 47 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0032others(44): Show | 55 | HG00408.hp2 HG00558.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.553-157delT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr11 | 86257340 | |||||
chr11:86257358
|
T | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.553-157T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86257358 | ||||||
chr11:86257439
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.553-76C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 5/11 | chr11 | 86257439 | ||||||
chr11:86257697
|
A | G | 1 | a0001c0002t0001g0182 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.634+101A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86257697 | ||||||
chr11:86257706
|
A | C | 1 | a0001c0001t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.634+110A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86257706 | ||||||
chr11:86257710
|
G | C | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+114G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86257710 | ||||||
chr11:86257794
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.634+198C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86257794 | ||||||
chr11:86257821
|
G | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.634+225G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86257821 | ||||||
chr11:86258075
|
T | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0071others(14): Show | 22 | HG01099.hp1 HG01255.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.634+479T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258075 | ||||||
chr11:86258163
|
TA | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0042others(53): Show | 72 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.634+575delA | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86258163 | |||||
chr11:86258505
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.634+909C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258505 | ||||||
chr11:86258536
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.634+940C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258536 | ||||||
chr11:86258543
|
C | T | 89 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0010others(86): Show | 116 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.634+947C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258543 | ||||||
chr11:86258554
|
G | GTTTT | 13 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0141others(10): Show | 15 | HG00438.hp2 HG02056.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.634+958_634+959ins others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258554 | ||||||
chr11:86258554
|
G | GTTTTT | 10 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0143others(7): Show | 13 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.634+958_634+959ins others(5): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258554 | ||||||
chr11:86258554
|
G | T | 3 | a0001c0002t0001g0246a0001c0002t0001g0247a0001c0002t0001g0248 | 3 | HG01106.hp1 HG01978.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.634+958G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258554 | ||||||
chr11:86258555
|
G | GT | 41 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(38): Show | 45 | HG01074.hp2 HG01884.hp2 HG02056.hp1 others(42): Show |
intron_variant | MODIFIER | c.634+976dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86258555 | |||||
chr11:86258555
|
G | T | 26 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(23): Show | 32 | HG00408.hp2 HG00438.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.634+959G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258555 | ||||||
chr11:86258762
|
G | T | 25 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(22): Show | 31 | HG00408.hp2 HG00438.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.634+1166G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258762 | ||||||
chr11:86258786
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.634+1190C>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258786 | ||||||
chr11:86258847
|
C | T | 4 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(1): Show | 4 | HG02976.hp2 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+1251C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258847 | ||||||
chr11:86258858
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0158 | 2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.634+1262T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86258858 | ||||||
chr11:86259129
|
A | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0089 | 2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.634+1533A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259129 | ||||||
chr11:86259223
|
T | TAAAAATC others(312): Show |
40 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0042others(37): Show | 55 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.634+1643_634+1644i others(321): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86259223 | |||||
chr11:86259223
|
T | TAAAAATC others(313): Show |
13 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0209others(10): Show | 14 | HG01069.hp2 HG01123.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.634+1643_634+1644i others(322): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86259223 | |||||
chr11:86259223
|
T | TAAAAATC others(314): Show |
1 | a0001c0001t0003g0220 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.634+1643_634+1644i others(323): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86259223 | |||||
chr11:86259223
|
T | TAAAAATC others(312): Show |
1 | a0001c0001t0001g0232 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.634+1643_634+1644i others(321): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86259223 | |||||
chr11:86259228
|
A | G | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+1632A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259228 | ||||||
chr11:86259251
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.634+1655G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259251 | ||||||
chr11:86259392
|
T | TG | 142 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0031others(139): Show | 178 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.634+1797dupG | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86259392 | |||||
chr11:86259409
|
T | G | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+1813T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259409 | ||||||
chr11:86259492
|
G | T | 1 | a0001c0002t0001g0193 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.634+1896G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259492 | ||||||
chr11:86259514
|
C | T | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+1918C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259514 | ||||||
chr11:86259515
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.634+1919C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259515 | ||||||
chr11:86259606
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0016others(199): Show | 255 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.634+2010T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259606 | ||||||
chr11:86259834
|
A | C | 1 | a0001c0001t0001g0156 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.634+2238A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259834 | ||||||
chr11:86259998
|
C | A | 1 | a0001c0002t0001g0263 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.634+2402C>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86259998 | ||||||
chr11:86260097
|
A | G | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+2501A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260097 | ||||||
chr11:86260176
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.634+2580A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260176 | ||||||
chr11:86260280
|
T | G | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+2684T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260280 | ||||||
chr11:86260380
|
C | G | 1 | a0001c0002t0001g0254 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.634+2784C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260380 | ||||||
chr11:86260403
|
A | AT | 203 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0016others(200): Show | 256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.634+2813dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86260403 | |||||
chr11:86260421
|
G | A | 1 | a0001c0002t0001g0263 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.634+2825G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260421 | ||||||
chr11:86260516
|
A | ACTGCACC others(4): Show |
203 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0016others(200): Show | 256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.634+2924_634+2925i others(13): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86260516 | |||||
chr11:86260695
|
A | C | 1 | a0001c0001t0001g0239 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.634+3099A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260695 | ||||||
chr11:86260823
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.634+3227T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260823 | ||||||
chr11:86260824
|
A | T | 1 | a0001c0001t0001g0116 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.634+3228A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260824 | ||||||
chr11:86260825
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.634+3229T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260825 | ||||||
chr11:86260844
|
A | T | 1 | a0001c0002t0001g0164 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.634+3248A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260844 | ||||||
chr11:86260900
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.635-3272G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260900 | ||||||
chr11:86260917
|
CT | C | 12 | a0001c0001t0001g0023a0001c0001t0001g0031a0001c0001t0001g0116others(9): Show | 14 | HG02572.hp1 HG02809.hp2 HG02896.hp2 others(11): Show |
intron_variant | MODIFIER | c.635-3243delT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86260917 | |||||
chr11:86260992
|
T | A | 9 | a0001c0001t0001g0031a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 10 | HG02572.hp1 HG02809.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.635-3180T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86260992 | ||||||
chr11:86261048
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.635-3124C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261048 | ||||||
chr11:86261090
|
A | G | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.635-3082A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261090 | ||||||
chr11:86261120
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0140a0001c0001t0001g0296 | 6 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.635-3052G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261120 | ||||||
chr11:86261152
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.635-3020C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261152 | ||||||
chr11:86261200
|
A | G | 7 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0062others(4): Show | 9 | NA18959.hp2 NA18967.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.635-2972A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261200 | ||||||
chr11:86261254
|
C | T | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.635-2918C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261254 | ||||||
chr11:86261274
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.635-2898C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261274 | ||||||
chr11:86261404
|
GC | G | 27 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.635-2764delC | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86261404 | |||||
chr11:86261436
|
C | T | 94 | a0001c0001t0001g0016a0001c0001t0001g0118a0001c0001t0001g0141others(91): Show | 122 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.635-2736C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261436 | ||||||
chr11:86261733
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.635-2439G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261733 | ||||||
chr11:86261752
|
C | T | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.635-2420C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261752 | ||||||
chr11:86261897
|
T | C | 142 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0031others(139): Show | 178 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.635-2275T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261897 | ||||||
chr11:86261963
|
A | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0129 | 2 | HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.635-2209A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86261963 | ||||||
chr11:86262176
|
C | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.635-1996C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86262176 | ||||||
chr11:86262547
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.635-1625C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86262547 | ||||||
chr11:86262578
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0206 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.635-1594A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86262578 | ||||||
chr11:86262599
|
C | T | 2 | a0001c0001t0001g0165a0001c0002t0001g0201 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.635-1573C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86262599 | ||||||
chr11:86262673
|
G | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.635-1499G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86262673 | ||||||
chr11:86262813
|
C | CT | 46 | a0001c0001t0001g0033a0001c0001t0001g0054a0001c0001t0001g0137others(43): Show | 60 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.635-1346dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86262813 | |||||
chr11:86262813
|
C | CTT | 55 | a0001c0001t0001g0016a0001c0001t0001g0118a0001c0001t0001g0141others(52): Show | 70 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.635-1347_635-1346d others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr11 | 86262813 | |||||
chr11:86262827
|
C | T | 142 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0031others(139): Show | 178 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.635-1345C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86262827 | ||||||
chr11:86262960
|
C | T | 5 | a0001c0002t0001g0177a0001c0002t0001g0181a0001c0002t0001g0191others(2): Show | 5 | HG00544.hp2 NA18941.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-1212C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86262960 | ||||||
chr11:86263033
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0100 | 2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.635-1139C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86263033 | ||||||
chr11:86263046
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.635-1126G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86263046 | ||||||
chr11:86263150
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.635-1022T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86263150 | ||||||
chr11:86263354
|
G | C | 1 | a0001c0002t0001g0243 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.635-818G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86263354 | ||||||
chr11:86263547
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.635-625A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86263547 | ||||||
chr11:86263932
|
T | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.635-240T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86263932 | ||||||
chr11:86264118
|
G | A | 1 | a0001c0002t0001g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.635-54G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 6/11 | chr11 | 86264118 | ||||||
chr11:86264295
|
A | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0120others(1): Show | 8 | HG00140.hp2 HG00280.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.726+32A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86264295 | ||||||
chr11:86264334
|
C | T | 1 | a0001c0002t0001g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.726+71C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86264334 | ||||||
chr11:86264439
|
A | ATATT | 116 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(113): Show | 146 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.726+190_726+193dup others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr11 | 86264439 | |||||
chr11:86264633
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.726+370G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86264633 | ||||||
chr11:86264730
|
A | G | 18 | a0001c0001t0001g0016a0001c0001t0001g0118a0001c0001t0001g0141others(15): Show | 23 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.726+467A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86264730 | ||||||
chr11:86264851
|
C | G | 6 | a0001c0001t0001g0027a0001c0001t0001g0069a0001c0001t0001g0079others(3): Show | 7 | HG00323.hp2 HG00738.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.726+588C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86264851 | ||||||
chr11:86265169
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.726+906A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86265169 | ||||||
chr11:86265320
|
C | G | 1 | a0001c0001t0001g0045 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.727-763C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86265320 | ||||||
chr11:86265439
|
G | A | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.727-644G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86265439 | ||||||
chr11:86265495
|
C | T | 27 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.727-588C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86265495 | ||||||
chr11:86265990
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.727-93A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86265990 | ||||||
chr11:86266075
|
G | A | 227 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
splice_region_variant&intron_variant | LOW | c.727-8G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 7/11 | chr11 | 86266075 | ||||||
chr11:86266497
|
T | C | 2 | a0001c0001t0002g0294a0001c0001t0002g0295 | 2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.860+281T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86266497 | ||||||
chr11:86266849
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0149 | 3 | HG01496.hp1 HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.860+633C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86266849 | ||||||
chr11:86266873
|
T | G | 1 | a0001c0001t0001g0102 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.860+657T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86266873 | ||||||
chr11:86266958
|
C | T | 142 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0031others(139): Show | 178 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.860+742C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86266958 | ||||||
chr11:86267144
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.860+928A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267144 | ||||||
chr11:86267156
|
G | A | 1 | a0001c0002t0001g0183 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.860+940G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267156 | ||||||
chr11:86267218
|
A | G | 1 | a0001c0002t0001g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.860+1002A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267218 | ||||||
chr11:86267394
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.861-1062A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267394 | ||||||
chr11:86267622
|
C | T | 142 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0031others(139): Show | 178 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.861-834C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267622 | ||||||
chr11:86267689
|
C | G | 1 | a0001c0002t0001g0190 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.861-767C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267689 | ||||||
chr11:86267692
|
G | C | 142 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0031others(139): Show | 178 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.861-764G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267692 | ||||||
chr11:86267766
|
A | AT | 11 | a0001c0001t0001g0027a0001c0001t0001g0056a0001c0001t0001g0068others(8): Show | 12 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.861-670dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 86267766 | |||||
chr11:86267766
|
A | ATT | 8 | a0001c0001t0001g0033a0001c0001t0001g0137a0001c0001t0001g0138others(5): Show | 9 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.861-671_861-670dup others(2): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 86267766 | |||||
chr11:86267766
|
A | ATTT | 55 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0042others(52): Show | 72 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.861-672_861-670dup others(3): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 86267766 | |||||
chr11:86267766
|
A | ATTTT | 126 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0031others(123): Show | 161 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.861-673_861-670dup others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 86267766 | |||||
chr11:86267766
|
A | ATTTTT | 13 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0151others(10): Show | 13 | HG02145.hp1 HG02970.hp1 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.861-674_861-670dup others(5): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr11 | 86267766 | |||||
chr11:86267821
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.861-635G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267821 | ||||||
chr11:86267932
|
G | T | 1 | a0001c0001t0001g0165 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.861-524G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267932 | ||||||
chr11:86267968
|
G | C | 115 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(112): Show | 145 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.861-488G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86267968 | ||||||
chr11:86268007
|
TG | T | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.861-448delG | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86268007 | ||||||
chr11:86268153
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0232a0001c0001t0004g0231 | 4 | HG02615.hp2 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-303C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86268153 | ||||||
chr11:86268194
|
C | T | 1 | a0001c0001t0001g0027 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.861-262C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86268194 | ||||||
chr11:86268228
|
T | G | 97 | a0001c0001t0001g0016a0001c0001t0001g0118a0001c0001t0001g0141others(94): Show | 125 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.861-228T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 8/11 | chr11 | 86268228 | ||||||
chr11:86268591
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.966+30C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86268591 | ||||||
chr11:86268594
|
C | CGT | 32 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0032others(29): Show | 40 | HG00558.hp1 HG01074.hp2 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.966+64_966+65dupGT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | |||||
chr11:86268594
|
C | CGTGT | 68 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(65): Show | 86 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.966+62_966+65dupGT others(2): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | |||||
chr11:86268594
|
C | CGTGTGT | 12 | a0001c0001t0001g0013a0001c0001t0001g0053a0001c0001t0001g0066others(9): Show | 17 | HG02027.hp2 HG02080.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.966+60_966+65dupGT others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | |||||
chr11:86268594
|
C | CGTGTGTG others(1): Show |
49 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0043others(46): Show | 62 | HG00140.hp1 HG00323.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.966+58_966+65dupGT others(6): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | |||||
chr11:86268594
|
C | CGTGTGTG others(3): Show |
6 | a0001c0001t0001g0158a0001c0001t0001g0209a0001c0001t0001g0215others(3): Show | 6 | HG00639.hp1 HG01175.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+56_966+65dupGT others(8): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | |||||
chr11:86268594
|
C | CGTGTGTG others(5): Show |
2 | a0001c0001t0001g0204a0001c0001t0001g0232 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.966+54_966+65dupGT others(10): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | |||||
chr11:86268594
|
C | CGTGTGTG others(15): Show |
1 | a0001c0002t0001g0170 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.966+44_966+65dupGT others(20): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | |||||
chr11:86268594
|
CGT | C | 41 | a0001c0001t0001g0028a0001c0001t0001g0060a0001c0001t0001g0091others(38): Show | 56 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.966+64_966+65delGT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268594 | |||||
chr11:86268601
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0048 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.966+49_966+50insAT others(8): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268601 | |||||
chr11:86268623
|
GTGTA | G | 3 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0135 | 3 | HG03471.hp1 HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.966+66_966+69delAT others(2): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268623 | |||||
chr11:86268624
|
TGTATGTG others(5): Show |
T | 1 | a0001c0001t0001g0049 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.966+65_966+76delTA others(10): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86268624 | |||||
chr11:86268627
|
A | G | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(15): Show | 21 | HG01074.hp2 HG01884.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.966+66A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86268627 | ||||||
chr11:86268636
|
C | T | 17 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0122others(14): Show | 19 | HG01074.hp2 HG01884.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.966+75C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86268636 | ||||||
chr11:86268910
|
T | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0018others(2): Show | 12 | HG00140.hp2 HG00280.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.966+349T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86268910 | ||||||
chr11:86269031
|
C | T | 142 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0031others(139): Show | 178 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.966+470C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269031 | ||||||
chr11:86269115
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.966+554G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269115 | ||||||
chr11:86269193
|
A | T | 18 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(15): Show | 25 | HG00741.hp1 HG01192.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.966+632A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269193 | ||||||
chr11:86269311
|
C | G | 1 | a0001c0001t0001g0137 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.966+750C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269311 | ||||||
chr11:86269432
|
A | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0099 | 2 | HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.966+871A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269432 | ||||||
chr11:86269773
|
A | C | 5 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0081others(2): Show | 6 | HG02258.hp1 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+1212A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269773 | ||||||
chr11:86269786
|
C | A | 52 | a0001c0001t0001g0016a0001c0001t0001g0118a0001c0002t0001g0005others(49): Show | 66 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.966+1225C>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269786 | ||||||
chr11:86269895
|
C | G | 1 | a0001c0002t0001g0192 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.966+1334C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269895 | ||||||
chr11:86269915
|
C | T | 5 | a0001c0001t0001g0033a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 6 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+1354C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269915 | ||||||
chr11:86269916
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0016others(200): Show | 256 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.966+1355A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269916 | ||||||
chr11:86269919
|
T | G | 1 | a0001c0002t0001g0241 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.966+1358T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86269919 | ||||||
chr11:86270126
|
A | G | 1 | a0001c0002t0001g0187 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.966+1565A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86270126 | ||||||
chr11:86270213
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.966+1652T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86270213 | ||||||
chr11:86270272
|
C | CTTAT | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.966+1715_966+1718d others(6): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86270272 | |||||
chr11:86270293
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.966+1732C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86270293 | ||||||
chr11:86270355
|
GT | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(271): Show | 364 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(361): Show |
intron_variant | MODIFIER | c.966+1810delT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86270355 | |||||
chr11:86270355
|
GTT | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0062others(6): Show | 12 | HG01496.hp2 HG01515.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.966+1809_966+1810d others(4): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86270355 | |||||
chr11:86270545
|
A | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0229 | 2 | HG01070.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.966+1984A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86270545 | ||||||
chr11:86270835
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.966+2274G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86270835 | ||||||
chr11:86271149
|
C | T | 27 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.966+2588C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86271149 | ||||||
chr11:86271269
|
A | C | 1 | a0001c0001t0001g0209 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.966+2708A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86271269 | ||||||
chr11:86271271
|
G | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.966+2710G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86271271 | ||||||
chr11:86271628
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.966+3067G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86271628 | ||||||
chr11:86271665
|
T | C | 33 | a0001c0001t0001g0001a0001c0001t0001g0042a0001c0001t0001g0043others(30): Show | 46 | HG00140.hp1 HG01069.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.966+3104T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86271665 | ||||||
chr11:86271941
|
C | CT | 39 | a0001c0001t0001g0207a0001c0002t0001g0002a0001c0002t0001g0020others(36): Show | 53 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.966+3390dupT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86271941 | |||||
chr11:86272056
|
A | ATTTTGTT others(896): Show |
13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(10): Show | 15 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(12): Show |
intron_variant | MODIFIER | c.966+3499_966+3500i others(905): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272056 | |||||
chr11:86272056
|
A | ATTTTGTT others(897): Show |
1 | a0001c0001t0001g0134 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.966+3499_966+3500i others(906): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272056 | |||||
chr11:86272056
|
A | ATTTTGTT others(897): Show |
3 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG02976.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.966+3499_966+3500i others(906): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272056 | |||||
chr11:86272056
|
A | ATTTTGTT others(898): Show |
1 | a0001c0001t0001g0123 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.966+3499_966+3500i others(907): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272056 | |||||
chr11:86272056
|
A | ATTTTTTT others(894): Show |
1 | a0001c0001t0001g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272056 | |||||
chr11:86272056
|
A | ATTTTTTT others(895): Show |
1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(904): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272056 | |||||
chr11:86272057
|
T | TTTTTTTT others(892): Show |
11 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0082others(8): Show | 16 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.966+3519_966+3520i others(901): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | |||||
chr11:86272057
|
T | TTTTTTTT others(893): Show |
1 | a0001c0001t0001g0096 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | |||||
chr11:86272057
|
T | TTTTTTTT others(893): Show |
38 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(35): Show | 51 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | |||||
chr11:86272057
|
T | TTTTTTTT others(894): Show |
1 | a0001c0002t0001g0275 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | |||||
chr11:86272057
|
T | TTTTTTTT others(894): Show |
1 | a0001c0001t0001g0092 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | |||||
chr11:86272057
|
T | TTTTTTTT others(894): Show |
38 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0013others(35): Show | 57 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | |||||
chr11:86272057
|
T | TTTTTTTT others(894): Show |
1 | a0001c0001t0001g0008 | 4 | HG01099.hp2 HG02451.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | |||||
chr11:86272057
|
T | TTTTTTTT others(895): Show |
2 | a0001c0001t0001g0054a0001c0001t0001g0120 | 2 | HG02280.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.966+3514_966+3515i others(904): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | |||||
chr11:86272057
|
T | TTTTTTTT others(896): Show |
1 | a0001c0001t0001g0154 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(905): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | |||||
chr11:86272057
|
T | TTTTTTTT others(897): Show |
1 | a0001c0001t0001g0147 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(906): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272057 | |||||
chr11:86272058
|
T | TTTTTTTT others(890): Show |
2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.966+3513_966+3514i others(899): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(892): Show |
1 | a0001c0002t0001g0277 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.966+3514_966+3515i others(901): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(892): Show |
1 | a0001c0002t0001g0188 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.966+3514_966+3515i others(901): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(892): Show |
2 | a0001c0001t0001g0048a0001c0001t0001g0286 | 3 | HG01256.hp2 HG01258.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.966+3514_966+3515i others(901): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(893): Show |
1 | a0001c0001t0001g0214 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(893): Show |
32 | a0001c0001t0001g0207a0001c0002t0001g0002a0001c0002t0001g0020others(29): Show | 45 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(893): Show |
1 | a0001c0002t0001g0040 | 2 | NA18977.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(893): Show |
45 | a0001c0001t0001g0016a0001c0001t0001g0118a0001c0001t0001g0141others(42): Show | 59 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(893): Show |
1 | a0001c0002t0001g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(893): Show |
10 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(7): Show | 10 | HG00323.hp1 HG00639.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(893): Show |
38 | a0001c0001t0001g0001a0001c0001t0001g0042a0001c0001t0001g0043others(35): Show | 52 | HG00140.hp1 HG01069.hp2 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(902): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(894): Show |
4 | a0001c0002t0001g0250a0001c0002t0001g0257a0001c0002t0001g0259others(1): Show | 4 | HG02074.hp1 HG03942.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(894): Show |
6 | a0001c0001t0001g0165a0001c0002t0001g0179a0001c0002t0001g0184others(3): Show | 6 | HG01981.hp2 HG03130.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(894): Show |
1 | a0001c0001t0001g0291 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(894): Show |
12 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0050others(9): Show | 14 | HG01175.hp2 HG01517.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(894): Show |
1 | a0001c0002t0001g0164 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(903): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(895): Show |
18 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(15): Show | 24 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.966+3514_966+3515i others(904): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(895): Show |
1 | a0001c0001t0001g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.966+3514_966+3515i others(904): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272058
|
T | TTTTTTTT others(896): Show |
3 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0156 | 3 | HG02027.hp1 NA19066.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.966+3514_966+3515i others(905): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272058 | |||||
chr11:86272059
|
T | TTTTTTTT others(891): Show |
1 | a0001c0002t0001g0172 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(900): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272059 | |||||
chr11:86272059
|
T | TTTTTTTT others(892): Show |
1 | a0001c0002t0001g0272 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.966+3514_966+3515i others(901): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272059 | |||||
chr11:86272061
|
T | TTTTTTTT others(890): Show |
1 | a0001c0001t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.966+3514_966+3515i others(899): Show |
EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86272061 | |||||
chr11:86272076
|
G | A | 2 | a0001c0001t0002g0294a0001c0001t0002g0295 | 2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.966+3515G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272076 | ||||||
chr11:86272092
|
C | G | 94 | a0001c0001t0001g0016a0001c0001t0001g0118a0001c0001t0001g0141others(91): Show | 122 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.966+3531C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272092 | ||||||
chr11:86272118
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.966+3557C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272118 | ||||||
chr11:86272218
|
C | T | 2 | a0001c0001t0001g0207a0001c0002t0001g0256 | 2 | HG02015.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.966+3657C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272218 | ||||||
chr11:86272279
|
C | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0204 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.966+3718C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272279 | ||||||
chr11:86272304
|
T | C | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.966+3743T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272304 | ||||||
chr11:86272317
|
C | T | 5 | a0001c0002t0001g0047a0001c0002t0001g0253a0001c0002t0001g0254others(2): Show | 6 | HG02056.hp1 NA18952.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.966+3756C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272317 | ||||||
chr11:86272338
|
G | A | 5 | a0001c0001t0001g0033a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 6 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.966+3777G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272338 | ||||||
chr11:86272406
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.966+3845C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272406 | ||||||
chr11:86272455
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0078 | 2 | HG03831.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.966+3894A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272455 | ||||||
chr11:86272556
|
G | T | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.966+3995G>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272556 | ||||||
chr11:86272565
|
T | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0095 | 2 | NA19068.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.966+4004T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272565 | ||||||
chr11:86272661
|
A | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0229 | 2 | HG01070.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.966+4100A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272661 | ||||||
chr11:86272907
|
T | A | 1 | a0001c0002t0001g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.967-4073T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272907 | ||||||
chr11:86272927
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.967-4053T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86272927 | ||||||
chr11:86273148
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.967-3832C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86273148 | ||||||
chr11:86273257
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.967-3723A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86273257 | ||||||
chr11:86273347
|
T | G | 3 | a0001c0001t0001g0109a0001c0001t0001g0113a0001c0001t0001g0114 | 3 | NA18993.hp1 NA19003.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.967-3633T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86273347 | ||||||
chr11:86273694
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.967-3286T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86273694 | ||||||
chr11:86273880
|
T | C | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-3100T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86273880 | ||||||
chr11:86273905
|
A | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0057 | 3 | HG00741.hp1 HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.967-3075A>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86273905 | ||||||
chr11:86274057
|
A | G | 2 | a0001c0002t0001g0251a0001c0002t0001g0274 | 2 | NA18950.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.967-2923A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274057 | ||||||
chr11:86274101
|
CT | C | 19 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(16): Show | 21 | HG01074.hp2 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.967-2866delT | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr11 | 86274101 | |||||
chr11:86274157
|
T | G | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-2823T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274157 | ||||||
chr11:86274194
|
T | G | 1 | a0001c0001t0001g0111 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.967-2786T>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274194 | ||||||
chr11:86274203
|
T | C | 5 | a0001c0001t0001g0033a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 6 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.967-2777T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274203 | ||||||
chr11:86274455
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.967-2525C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274455 | ||||||
chr11:86274488
|
C | G | 1 | a0001c0001t0001g0208 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.967-2492C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274488 | ||||||
chr11:86274635
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0158 | 2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.967-2345C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274635 | ||||||
chr11:86274661
|
G | C | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-2319G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274661 | ||||||
chr11:86274696
|
C | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0206 | 5 | HG00544.hp1 HG03209.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.967-2284C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274696 | ||||||
chr11:86274697
|
C | G | 2 | a0001c0002t0001g0046a0001c0002t0001g0252 | 3 | HG01346.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.967-2283C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274697 | ||||||
chr11:86274758
|
A | G | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-2222A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274758 | ||||||
chr11:86274811
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.967-2169G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86274811 | ||||||
chr11:86275005
|
A | G | 24 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(21): Show | 38 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.967-1975A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275005 | ||||||
chr11:86275070
|
G | C | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-1910G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275070 | ||||||
chr11:86275090
|
T | A | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-1890T>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275090 | ||||||
chr11:86275202
|
T | C | 2 | a0001c0002t0001g0265a0001c0002t0001g0271 | 2 | HG01255.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.967-1778T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275202 | ||||||
chr11:86275203
|
G | A | 2 | a0001c0002t0001g0265a0001c0002t0001g0271 | 2 | HG01255.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.967-1777G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275203 | ||||||
chr11:86275367
|
G | A | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-1613G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275367 | ||||||
chr11:86275411
|
C | A | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-1569C>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275411 | ||||||
chr11:86275476
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(225): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.967-1504G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275476 | ||||||
chr11:86275601
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.967-1379A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275601 | ||||||
chr11:86275618
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.967-1362C>T | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275618 | ||||||
chr11:86275745
|
T | C | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-1235T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275745 | ||||||
chr11:86275846
|
G | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0035others(24): Show | 33 | HG00408.hp2 HG01496.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.967-1134G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86275846 | ||||||
chr11:86276022
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.967-958G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86276022 | ||||||
chr11:86276146
|
C | G | 18 | a0001c0001t0001g0016a0001c0001t0001g0118a0001c0001t0001g0141others(15): Show | 23 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.967-834C>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86276146 | ||||||
chr11:86276488
|
A | G | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-492A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86276488 | ||||||
chr11:86276548
|
G | A | 18 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0049others(15): Show | 20 | HG01074.hp2 HG01884.hp2 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.967-432G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86276548 | ||||||
chr11:86276563
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.967-417G>A | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86276563 | ||||||
chr11:86276776
|
A | C | 30 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0018others(27): Show | 40 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.967-204A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 9/11 | chr11 | 86276776 | ||||||
chr11:86277184
|
A | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0080a0001c0001t0001g0099 | 4 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+46A>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 10/11 | chr11 | 86277184 | ||||||
chr11:86277585
|
A | G | 5 | a0001c0001t0001g0033a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 6 | HG02257.hp1 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126-333A>G | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 10/11 | chr11 | 86277585 | ||||||
chr11:86277788
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1126-130G>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 10/11 | chr11 | 86277788 | ||||||
chr11:86278001
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1199+10T>C | EED | ENSG00000074266.23 | transcript | ENST00000263360.11 | protein_coding | 11/11 | chr11 | 86278001 |