geneid | 10455 |
---|---|
ensemblid | ENSG00000198721.13 |
hgncid | 14601 |
symbol | ECI2 |
name | enoyl-CoA delta isomerase 2 |
refseq_nuc | NM_206836.3 |
refseq_prot | NP_996667.2 |
ensembl_nuc | ENST00000380118.8 |
ensembl_prot | ENSP00000369461.3 |
mane_status | MANE Select |
chr | chr6 |
start | 4115706 |
end | 4135575 |
strand | - |
ver | v1.2 |
region | chr6:4115706-4135575 |
region5000 | chr6:4110706-4140575 |
regionname0 | ECI2_chr6_4115706_4135575 |
regionname5000 | ECI2_chr6_4110706_4140575 |
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 | 394 | 218 | 58 | 41 | 89 | 4 | 24 | 74 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0002 | 0/0 | 394 | 107 | 18 | 17 | 65 | 3 | 4 | 50 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0003 | 0/0 | 394 | 32 | 8 | 13 | 2 | 5 | 4 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0004 | 0/0 | 394 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0005 | 0/0 | 394 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0006 | 0/0 | 394 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0007 | 0/0 | 394 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0008 | 0/0 | 394 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0009 | 0/0 | 394 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0010 | 0/0 | 394 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1185 | 193 | 33 | 41 | 89 | 4 | 24 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
c0002 | 0/0 | 1185 | 107 | 18 | 17 | 65 | 3 | 4 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
c0003 | 0/0 | 1185 | 32 | 8 | 13 | 2 | 5 | 4 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
c0004 | 0/0 | 1185 | 11 | 11 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
c0005 | 0/0 | 1185 | 8 | 8 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
c0006 | 0/0 | 1185 | 5 | 5 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
c0007 | 0/0 | 1185 | 4 | 0 | 0 | 4 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
c0008 | 0/0 | 1185 | 3 | 0 | 0 | 3 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
c0009 | 0/0 | 1185 | 2 | 2 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
c0010 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
c0011 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
c0012 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
c0013 | 0/0 | 1185 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
c0014 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
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 | 184 | 360 | 82 | 71 | 162 | 12 | 31 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
t0002 | 0/0 | 184 | 5 | 5 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
t0003 | 0/0 | 184 | 2 | 0 | 1 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
t0004 | 0/0 | 184 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
t0005 | 0/0 | 184 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
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 | 0/1 | 71 | 2 | 19 | 40 | 4 | 5 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0002 | 0/0 | 30 | 0 | 1 | 27 | 2 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0003 | 0/0 | 27 | 2 | 2 | 21 | 0 | 2 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0004 | 0/0 | 17 | 0 | 9 | 8 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0005 | 0/0 | 11 | 2 | 5 | 0 | 1 | 3 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0006 | 0/0 | 10 | 1 | 3 | 6 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0007 | 0/0 | 9 | 5 | 2 | 0 | 0 | 2 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0008 | 0/0 | 8 | 0 | 5 | 0 | 3 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0009 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0010 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0016 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0023 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0032 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1185 | 193 | 33 | 41 | 89 | 4 | 24 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0001c0004 | 0/0 | 1185 | 11 | 11 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0001c0005 | 0/0 | 1185 | 8 | 8 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0001c0006 | 0/0 | 1185 | 5 | 5 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0001c0012 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0002c0002 | 0/0 | 1185 | 107 | 18 | 17 | 65 | 3 | 4 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0003c0003 | 0/0 | 1185 | 32 | 8 | 13 | 2 | 5 | 4 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0004c0007 | 0/0 | 1185 | 4 | 0 | 0 | 4 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0005c0008 | 0/0 | 1185 | 3 | 0 | 0 | 3 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0006c0009 | 0/0 | 1185 | 2 | 2 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0007c0010 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0008c0011 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0009c0013 | 0/0 | 1185 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0010c0014 | 0/0 | 1185 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1368 | 189 | 33 | 40 | 87 | 4 | 23 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0001c0001t0003 | 0/0 | 1368 | 2 | 0 | 1 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0001c0001t0004 | 0/0 | 1368 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0001c0004t0001 | 0/0 | 1368 | 11 | 11 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0001c0005t0001 | 0/0 | 1368 | 8 | 8 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0001c0006t0002 | 0/0 | 1368 | 4 | 4 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0001c0006t0005 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0001c0012t0001 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0002c0002t0001 | 0/0 | 1368 | 107 | 18 | 17 | 65 | 3 | 4 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0003c0003t0001 | 0/0 | 1368 | 32 | 8 | 13 | 2 | 5 | 4 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0004c0007t0001 | 0/0 | 1368 | 4 | 0 | 0 | 4 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0005c0008t0001 | 0/0 | 1368 | 3 | 0 | 0 | 3 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0006c0009t0001 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0006c0009t0002 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0007c0010t0001 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0008c0011t0001 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0009c0013t0001 | 0/0 | 1368 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
a0010c0014t0001 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | copy fasta | chr6 | 4110706 | 4140575 |
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 | 0/1 | 71 | 2 | 19 | 40 | 4 | 5 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0003 | 0/0 | 27 | 2 | 2 | 21 | 0 | 2 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0006 | 0/0 | 10 | 1 | 3 | 6 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0007 | 0/0 | 9 | 5 | 2 | 0 | 0 | 2 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0010 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0023 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0001t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0004t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0004t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0005t0001g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0005t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0005t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0006t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0006t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0006t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0001c0012t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0002 | 0/0 | 30 | 0 | 1 | 27 | 2 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0004 | 0/0 | 17 | 0 | 9 | 8 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0009 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0003c0003t0001g0005 | 0/0 | 11 | 2 | 5 | 0 | 1 | 3 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0003c0003t0001g0008 | 0/0 | 8 | 0 | 5 | 0 | 3 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0003c0003t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0003c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0003c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0003c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0003c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0003c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0003c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0003c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0003c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0004c0007t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0004c0007t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0005c0008t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0005c0008t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0006c0009t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0006c0009t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0007c0010t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0008c0011t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0009c0013t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
a0010c0014t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00140 | hp2 | a0003 | c0003 | t0001 | g0008 | EUR | GBR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0032 | EUR | FIN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00323 | hp2 | a0003 | c0003 | t0001 | g0121 | EUR | FIN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00558 | hp1 | a0005 | c0008 | t0001 | g0026 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00735 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01109 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0065 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01192 | hp2 | a0003 | c0003 | t0001 | g0008 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01346 | hp2 | a0003 | c0003 | t0001 | g0005 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01358 | hp2 | a0003 | c0003 | t0001 | g0118 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01433 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01496 | hp1 | a0003 | c0003 | t0001 | g0120 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01496 | hp2 | a0009 | c0013 | t0001 | g0107 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01515 | hp2 | a0003 | c0003 | t0001 | g0008 | EUR | IBS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01516 | hp2 | a0003 | c0003 | t0001 | g0005 | EUR | IBS | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01884 | hp1 | a0001 | c0004 | t0001 | g0014 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01891 | hp1 | a0001 | c0004 | t0001 | g0014 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01943 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01993 | hp2 | a0003 | c0003 | t0001 | g0005 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02004 | hp2 | a0003 | c0003 | t0001 | g0116 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02055 | hp2 | a0010 | c0014 | t0001 | g0129 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02071 | hp2 | a0003 | c0003 | t0001 | g0119 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02145 | hp2 | a0001 | c0004 | t0001 | g0075 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02257 | hp1 | a0001 | c0012 | t0001 | g0077 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0014 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02258 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02273 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02280 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02293 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0126 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02615 | hp2 | a0001 | c0004 | t0001 | g0076 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02622 | hp1 | a0003 | c0003 | t0001 | g0005 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02717 | hp1 | a0001 | c0005 | t0001 | g0074 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02723 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02723 | hp2 | a0006 | c0009 | t0001 | g0068 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02818 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0128 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02895 | hp2 | a0001 | c0005 | t0001 | g0011 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02896 | hp2 | a0001 | c0005 | t0001 | g0011 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02922 | hp2 | a0001 | c0005 | t0001 | g0011 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02965 | hp1 | a0003 | c0003 | t0001 | g0079 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02965 | hp2 | a0007 | c0010 | t0001 | g0071 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02970 | hp1 | a0006 | c0009 | t0002 | g0039 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02976 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03017 | hp2 | a0003 | c0003 | t0001 | g0117 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0127 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03195 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03209 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0013 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03239 | hp1 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03486 | hp1 | a0003 | c0003 | t0001 | g0114 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03490 | hp1 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03492 | hp2 | a0003 | c0003 | t0001 | g0005 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03516 | hp1 | a0001 | c0006 | t0002 | g0018 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03540 | hp1 | a0003 | c0003 | t0001 | g0113 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03540 | hp2 | a0001 | c0006 | t0002 | g0041 | AFR | GWD | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03579 | hp1 | a0001 | c0005 | t0001 | g0073 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | STU | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0027 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | BEB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0063 | SAS | STU | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18522 | hp1 | a0001 | c0004 | t0001 | g0014 | AFR | YRI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0125 | AFR | YRI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | CHB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | CHB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18906 | hp2 | a0001 | c0006 | t0002 | g0018 | AFR | YRI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18943 | hp2 | a0003 | c0003 | t0001 | g0122 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18951 | hp1 | a0005 | c0008 | t0001 | g0026 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18959 | hp2 | a0004 | c0007 | t0001 | g0020 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18988 | hp1 | a0008 | c0011 | t0001 | g0050 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18999 | hp2 | a0004 | c0007 | t0001 | g0046 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19003 | hp2 | a0004 | c0007 | t0001 | g0020 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | LWK | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19030 | hp2 | a0001 | c0006 | t0002 | g0018 | AFR | LWK | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | LWK | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19058 | hp2 | a0005 | c0008 | t0001 | g0042 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19085 | hp2 | a0004 | c0007 | t0001 | g0020 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19240 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | YRI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA19240 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | YRI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA20129 | hp1 | a0001 | c0006 | t0005 | g0040 | AFR | ASW | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA20805 | hp1 | a0003 | c0003 | t0001 | g0008 | EUR | TSI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01123 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0124 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02559 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | USA | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA20300 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | USA | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0095 | REF | REF | ECI2_chr6_4110706_4140575 | ECI2 | chr6 | 4110706 | 4140575 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:4116028
|
G | A | 6 | a0002a0003a0004others(3): Show | 148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
missense_variant&splice_region_variant | MODERATE | c.1031C>T | p.Ala344Val | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 10/10 | 1046/1368 | 1031/1185 | 344/394 | chr6 | 4116028 | ||
chr6:4117373
|
G | A | 1 | a0006 | 2 | HG02723.hp2 HG02970.hp1 |
missense_variant | MODERATE | c.964C>T | p.Pro322Ser | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/10 | 979/1368 | 964/1185 | 322/394 | chr6 | 4117373 | ||
chr6:4125269
|
G | A | 1 | a0007 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.776C>T | p.Ala259Val | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/10 | 791/1368 | 776/1185 | 259/394 | chr6 | 4125269 | ||
chr6:4125317
|
T | C | 1 | a0008 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.728A>G | p.Asn243Ser | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/10 | 743/1368 | 728/1185 | 243/394 | chr6 | 4125317 | ||
chr6:4126145
|
C | T | 1 | a0005 | 3 | HG00558.hp1 NA18951.hp1 NA19058.hp2 |
missense_variant | MODERATE | c.664G>A | p.Val222Ile | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/10 | 679/1368 | 664/1185 | 222/394 | chr6 | 4126145 | ||
chr6:4126225
|
T | C | 1 | a0004 | 4 | NA18959.hp2 NA18999.hp2 NA19003.hp2 others(1): Show |
missense_variant | MODERATE | c.584A>G | p.Tyr195Cys | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/10 | 599/1368 | 584/1185 | 195/394 | chr6 | 4126225 | ||
chr6:4133621
|
C | T | 1 | a0003 | 32 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(29): Show |
missense_variant | MODERATE | c.141G>A | p.Met47Ile | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/10 | 156/1368 | 141/1185 | 47/394 | chr6 | 4133621 | ||
chr6:4133656
|
T | C | 1 | a0009 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.106A>G | p.Met36Val | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/10 | 121/1368 | 106/1185 | 36/394 | chr6 | 4133656 | ||
chr6:4135520
|
G | C | 1 | a0010 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.41C>G | p.Ser14Trp | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/10 | 56/1368 | 41/1185 | 14/394 | chr6 | 4135520 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:4117413
|
C | T | 2 | a0001c0005a0001c0012 | 9 | HG02257.hp1 HG02717.hp1 HG02895.hp2 others(6): Show |
synonymous_variant | LOW | c.924G>A | p.Ala308Ala | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/10 | 939/1368 | 924/1185 | 308/394 | chr6 | 4117413 | ||
chr6:4119258
|
T | C | 3 | a0001c0004a0001c0005a0001c0012 | 20 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(17): Show |
synonymous_variant | LOW | c.813A>G | p.Pro271Pro | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/10 | 828/1368 | 813/1185 | 271/394 | chr6 | 4119258 | ||
chr6:4125334
|
A | G | 1 | a0005c0008 | 3 | HG00558.hp1 NA18951.hp1 NA19058.hp2 |
synonymous_variant | LOW | c.711T>C | p.Pro237Pro | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/10 | 726/1368 | 711/1185 | 237/394 | chr6 | 4125334 | ||
chr6:4126146
|
G | A | 2 | a0001c0006a0006c0009 | 7 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(4): Show |
synonymous_variant | LOW | c.663C>T | p.Ala221Ala | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/10 | 678/1368 | 663/1185 | 221/394 | chr6 | 4126146 | ||
chr6:4133564
|
G | A | 1 | a0001c0012 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.198C>T | p.Tyr66Tyr | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/10 | 213/1368 | 198/1185 | 66/394 | chr6 | 4133564 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:4115714
|
C | T | 1 | a0001c0001t0004 | 2 | NA18955.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*160G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 10/10 | 160 | chr6 | 4115714 | |||||
chr6:4115746
|
A | G | 1 | a0001c0001t0003 | 2 | HG01243.hp1 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*128T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 10/10 | 128 | chr6 | 4115746 | |||||
chr6:4115789
|
A | G | 1 | a0001c0006t0005 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*85T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 10/10 | 85 | chr6 | 4115789 | |||||
chr6:4135571
|
G | T | 3 | a0001c0006t0002a0001c0006t0005a0006c0009t0002 | 6 | HG02970.hp1 HG03516.hp1 HG03540.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-11C>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/10 | 11 | chr6 | 4135571 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:4116032
|
G | A | 10 | a0002c0002t0001g0004a0002c0002t0001g0021a0002c0002t0001g0031others(7): Show | 30 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(27): Show |
splice_region_variant&intron_variant | LOW | c.1030-3C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116032 | ||||||
chr6:4116071
|
G | C | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1030-42C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116071 | ||||||
chr6:4116106
|
T | G | 32 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(29): Show | 98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1030-77A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116106 | ||||||
chr6:4116107
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1030-78A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116107 | ||||||
chr6:4116134
|
T | C | 2 | a0001c0006t0002g0041a0001c0006t0005g0040 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1030-105A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116134 | ||||||
chr6:4116171
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1030-142A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116171 | ||||||
chr6:4116177
|
C | A | 1 | a0002c0002t0001g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1030-148G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116177 | ||||||
chr6:4116307
|
C | T | 1 | a0001c0001t0001g0029 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1030-278G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116307 | ||||||
chr6:4116351
|
A | C | 1 | a0002c0002t0001g0027 | 2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1030-322T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116351 | ||||||
chr6:4116444
|
CT | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(123): Show | 367 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.1030-416delA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116444 | ||||||
chr6:4116480
|
G | A | 1 | a0002c0002t0001g0125 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1030-451C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116480 | ||||||
chr6:4116535
|
G | C | 32 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(29): Show | 98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1030-506C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116535 | ||||||
chr6:4116586
|
C | T | 9 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(6): Show | 27 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1030-557G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116586 | ||||||
chr6:4116587
|
G | A | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1030-558C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116587 | ||||||
chr6:4116588
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1030-559G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116588 | ||||||
chr6:4116824
|
G | A | 1 | a0002c0002t0001g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1029+484C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4116824 | ||||||
chr6:4117080
|
G | GC | 62 | a0001c0006t0002g0018a0001c0006t0002g0041a0001c0006t0005g0040others(59): Show | 155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1029+227dupG | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 9/9 | chr6 | 4117080 | ||||||
chr6:4118161
|
G | T | 1 | a0002c0002t0001g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.886-710C>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118161 | ||||||
chr6:4118180
|
G | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(6): Show | 27 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.886-729C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118180 | ||||||
chr6:4118257
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0090others(1): Show | 9 | HG01167.hp1 HG01175.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.886-806G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118257 | ||||||
chr6:4118440
|
T | C | 57 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(54): Show | 148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.885+746A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118440 | ||||||
chr6:4118523
|
T | C | 5 | a0001c0006t0002g0018a0001c0006t0002g0041a0001c0006t0005g0040others(2): Show | 7 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.885+663A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118523 | ||||||
chr6:4118555
|
G | A | 56 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(53): Show | 147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.885+631C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118555 | ||||||
chr6:4118695
|
G | A | 1 | a0001c0001t0001g0029 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.885+491C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118695 | ||||||
chr6:4118745
|
C | T | 17 | a0002c0002t0001g0078a0002c0002t0001g0084a0002c0002t0001g0124others(14): Show | 36 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.885+441G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118745 | ||||||
chr6:4118750
|
T | G | 25 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0038others(22): Show | 50 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.885+436A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118750 | ||||||
chr6:4118783
|
C | T | 8 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0038others(5): Show | 14 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.885+403G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118783 | ||||||
chr6:4118795
|
T | C | 32 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(29): Show | 98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.885+391A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118795 | ||||||
chr6:4118817
|
C | T | 56 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(53): Show | 147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.885+369G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 8/9 | chr6 | 4118817 | ||||||
chr6:4119282
|
A | G | 84 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(81): Show | 208 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(205): Show |
splice_region_variant&intron_variant | LOW | c.796-7T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119282 | ||||||
chr6:4119319
|
AT | A | 36 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(33): Show | 89 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.796-45delA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119319 | ||||||
chr6:4119319
|
ATT | A | 45 | a0001c0001t0001g0067a0001c0012t0001g0077a0002c0002t0001g0002others(42): Show | 116 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.796-46_796-45delAA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119319 | ||||||
chr6:4119409
|
C | T | 1 | a0002c0002t0001g0127 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.796-134G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119409 | ||||||
chr6:4119424
|
G | A | 1 | a0001c0001t0001g0030 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.796-149C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119424 | ||||||
chr6:4119430
|
C | G | 1 | a0001c0001t0001g0010 | 7 | HG01167.hp2 HG01169.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.796-155G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119430 | ||||||
chr6:4119470
|
G | A | 56 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(53): Show | 147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.796-195C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119470 | ||||||
chr6:4119501
|
C | A | 11 | a0002c0002t0001g0004a0002c0002t0001g0021a0002c0002t0001g0031others(8): Show | 31 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.796-226G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119501 | ||||||
chr6:4119502
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.796-227C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119502 | ||||||
chr6:4119616
|
T | A | 8 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0030others(5): Show | 20 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.796-341A>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119616 | ||||||
chr6:4119654
|
A | G | 1 | a0002c0002t0001g0047 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.796-379T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119654 | ||||||
chr6:4119762
|
T | C | 59 | a0001c0006t0002g0041a0001c0006t0005g0040a0002c0002t0001g0002others(56): Show | 150 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.796-487A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119762 | ||||||
chr6:4119780
|
C | T | 1 | a0002c0002t0001g0025 | 3 | HG02109.hp1 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.796-505G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119780 | ||||||
chr6:4119823
|
T | A | 32 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(29): Show | 98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.796-548A>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119823 | ||||||
chr6:4119824
|
T | G | 3 | a0001c0004t0001g0013a0001c0004t0001g0075a0001c0004t0001g0076 | 7 | HG02145.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.796-549A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119824 | ||||||
chr6:4119926
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0033 | 6 | NA18949.hp1 NA18978.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.796-651A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119926 | ||||||
chr6:4119947
|
A | C | 57 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(54): Show | 148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.796-672T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4119947 | ||||||
chr6:4120022
|
T | C | 5 | a0001c0006t0002g0018a0001c0006t0002g0041a0001c0006t0005g0040others(2): Show | 7 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.796-747A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120022 | ||||||
chr6:4120067
|
T | C | 2 | a0002c0002t0001g0124a0002c0002t0001g0126 | 2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.796-792A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120067 | ||||||
chr6:4120077
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.796-802A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120077 | ||||||
chr6:4120094
|
T | G | 1 | a0003c0003t0001g0118 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.796-819A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120094 | ||||||
chr6:4120317
|
C | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070 | 3 | HG02622.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.796-1042G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120317 | ||||||
chr6:4120331
|
A | T | 62 | a0001c0006t0002g0018a0001c0006t0002g0041a0001c0006t0005g0040others(59): Show | 155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.796-1056T>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120331 | ||||||
chr6:4120333
|
C | G | 62 | a0001c0006t0002g0018a0001c0006t0002g0041a0001c0006t0005g0040others(59): Show | 155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.796-1058G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120333 | ||||||
chr6:4120449
|
G | A | 56 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(53): Show | 147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.796-1174C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120449 | ||||||
chr6:4120491
|
C | T | 1 | a0001c0001t0001g0010 | 7 | HG01167.hp2 HG01169.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.796-1216G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120491 | ||||||
chr6:4120506
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.796-1231G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120506 | ||||||
chr6:4120516
|
C | G | 1 | a0001c0001t0001g0010 | 7 | HG01167.hp2 HG01169.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.796-1241G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120516 | ||||||
chr6:4120630
|
G | A | 20 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0012others(17): Show | 66 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.796-1355C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120630 | ||||||
chr6:4120694
|
T | C | 4 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0075others(1): Show | 11 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.796-1419A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120694 | ||||||
chr6:4120729
|
A | C | 1 | a0002c0002t0001g0125 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.796-1454T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120729 | ||||||
chr6:4120764
|
A | C | 2 | a0001c0006t0002g0041a0001c0006t0005g0040 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.796-1489T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4120764 | ||||||
chr6:4121059
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.796-1784T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121059 | ||||||
chr6:4121099
|
C | T | 24 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0038others(21): Show | 49 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.796-1824G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121099 | ||||||
chr6:4121241
|
C | T | 1 | a0002c0002t0001g0045 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.796-1966G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121241 | ||||||
chr6:4121325
|
G | T | 1 | a0001c0001t0001g0034 | 2 | HG00423.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.796-2050C>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121325 | ||||||
chr6:4121388
|
G | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070 | 3 | HG02622.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.796-2113C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121388 | ||||||
chr6:4121546
|
C | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070 | 3 | HG02622.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.796-2271G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121546 | ||||||
chr6:4121597
|
T | C | 57 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(54): Show | 148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.796-2322A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121597 | ||||||
chr6:4121608
|
T | C | 4 | a0001c0005t0001g0011a0001c0005t0001g0073a0001c0005t0001g0074others(1): Show | 9 | HG02257.hp1 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.796-2333A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121608 | ||||||
chr6:4121693
|
GT | G | 26 | a0001c0001t0001g0089a0002c0002t0001g0017a0002c0002t0001g0025others(23): Show | 51 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.796-2419delA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121693 | ||||||
chr6:4121693
|
GTT | G | 31 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(28): Show | 97 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.796-2420_796-2419d others(4): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121693 | ||||||
chr6:4121695
|
T | G | 4 | a0003c0003t0001g0008a0003c0003t0001g0116a0003c0003t0001g0120others(1): Show | 11 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.796-2420A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121695 | ||||||
chr6:4121780
|
G | A | 1 | a0003c0003t0001g0122 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.796-2505C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121780 | ||||||
chr6:4121924
|
T | C | 2 | a0001c0006t0002g0018a0003c0003t0001g0117 | 4 | HG03017.hp2 HG03516.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.796-2649A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4121924 | ||||||
chr6:4122015
|
C | A | 62 | a0001c0006t0002g0018a0001c0006t0002g0041a0001c0006t0005g0040others(59): Show | 155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.796-2740G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122015 | ||||||
chr6:4122045
|
A | G | 4 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0075others(1): Show | 11 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.796-2770T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122045 | ||||||
chr6:4122144
|
C | T | 5 | a0001c0006t0002g0018a0001c0006t0002g0041a0001c0006t0005g0040others(2): Show | 7 | HG02723.hp2 HG02970.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.796-2869G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122144 | ||||||
chr6:4122153
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.796-2878C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122153 | ||||||
chr6:4122170
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.796-2895G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122170 | ||||||
chr6:4122224
|
C | CT | 60 | a0001c0001t0001g0087a0001c0006t0002g0018a0001c0006t0002g0041others(57): Show | 153 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.796-2950dupA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122224 | ||||||
chr6:4122250
|
T | C | 12 | a0002c0002t0001g0004a0002c0002t0001g0021a0002c0002t0001g0031others(9): Show | 32 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.796-2975A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122250 | ||||||
chr6:4122346
|
G | T | 2 | a0004c0007t0001g0020a0004c0007t0001g0046 | 4 | NA18959.hp2 NA18999.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+2904C>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122346 | ||||||
chr6:4122352
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.795+2898A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122352 | ||||||
chr6:4122371
|
C | A | 1 | a0002c0002t0001g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.795+2879G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122371 | ||||||
chr6:4122812
|
G | A | 32 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(29): Show | 98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.795+2438C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122812 | ||||||
chr6:4122843
|
G | A | 1 | a0002c0002t0001g0048 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.795+2407C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4122843 | ||||||
chr6:4123050
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.795+2200A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123050 | ||||||
chr6:4123147
|
T | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070 | 3 | HG02622.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.795+2103A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123147 | ||||||
chr6:4123207
|
C | T | 32 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(29): Show | 98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.795+2043G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123207 | ||||||
chr6:4123240
|
G | C | 1 | a0001c0001t0001g0029 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.795+2010C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123240 | ||||||
chr6:4123286
|
C | G | 4 | a0001c0005t0001g0011a0001c0005t0001g0073a0001c0005t0001g0074others(1): Show | 9 | HG02257.hp1 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.795+1964G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123286 | ||||||
chr6:4123308
|
C | G | 4 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0075others(1): Show | 11 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.795+1942G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123308 | ||||||
chr6:4123348
|
T | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(6): Show | 27 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.795+1902A>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123348 | ||||||
chr6:4123617
|
G | A | 1 | a0001c0001t0001g0029 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.795+1633C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123617 | ||||||
chr6:4123826
|
C | T | 1 | a0002c0002t0001g0064 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.795+1424G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123826 | ||||||
chr6:4123838
|
A | T | 2 | a0006c0009t0001g0068a0006c0009t0002g0039 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.795+1412T>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123838 | ||||||
chr6:4123843
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.795+1407G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4123843 | ||||||
chr6:4124031
|
G | A | 32 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(29): Show | 98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.795+1219C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124031 | ||||||
chr6:4124074
|
T | A | 1 | a0001c0001t0001g0099 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.795+1176A>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124074 | ||||||
chr6:4124173
|
A | C | 1 | a0002c0002t0001g0044 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.795+1077T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124173 | ||||||
chr6:4124203
|
A | G | 4 | a0001c0005t0001g0011a0001c0005t0001g0073a0001c0005t0001g0074others(1): Show | 9 | HG02257.hp1 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.795+1047T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124203 | ||||||
chr6:4124245
|
T | G | 1 | a0001c0001t0001g0006 | 10 | HG01175.hp1 HG01975.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.795+1005A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124245 | ||||||
chr6:4124325
|
C | T | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.795+925G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124325 | ||||||
chr6:4124354
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.795+896G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124354 | ||||||
chr6:4124466
|
G | A | 1 | a0002c0002t0001g0049 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.795+784C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124466 | ||||||
chr6:4124545
|
G | A | 1 | a0002c0002t0001g0049 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.795+705C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124545 | ||||||
chr6:4124615
|
G | A | 7 | a0002c0002t0001g0004a0002c0002t0001g0031a0002c0002t0001g0060others(4): Show | 24 | HG01069.hp2 HG01070.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.795+635C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124615 | ||||||
chr6:4124627
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.795+623C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124627 | ||||||
chr6:4124644
|
G | A | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0070 | 3 | HG02622.hp2 HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.795+606C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124644 | ||||||
chr6:4124770
|
T | G | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.795+480A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124770 | ||||||
chr6:4124772
|
T | C | 1 | a0009c0013t0001g0107 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.795+478A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124772 | ||||||
chr6:4124965
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.795+285G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4124965 | ||||||
chr6:4125085
|
T | C | 1 | a0002c0002t0001g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.795+165A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4125085 | ||||||
chr6:4125240
|
G | A | 20 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0012others(17): Show | 66 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.795+10C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 7/9 | chr6 | 4125240 | ||||||
chr6:4125380
|
T | G | 1 | a0002c0002t0001g0125 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.675-10A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/9 | chr6 | 4125380 | ||||||
chr6:4125421
|
A | G | 57 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(54): Show | 148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.675-51T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/9 | chr6 | 4125421 | ||||||
chr6:4125707
|
A | G | 62 | a0001c0006t0002g0018a0001c0006t0002g0041a0001c0006t0005g0040others(59): Show | 155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.675-337T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/9 | chr6 | 4125707 | ||||||
chr6:4125773
|
C | G | 1 | a0001c0001t0001g0082 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.674+362G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/9 | chr6 | 4125773 | ||||||
chr6:4125801
|
G | A | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.674+334C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/9 | chr6 | 4125801 | ||||||
chr6:4125862
|
A | G | 3 | a0002c0002t0001g0019a0002c0002t0001g0043a0002c0002t0001g0053 | 5 | NA18955.hp1 NA18979.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.674+273T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/9 | chr6 | 4125862 | ||||||
chr6:4125863
|
G | A | 83 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(80): Show | 207 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.674+272C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 6/9 | chr6 | 4125863 | ||||||
chr6:4126400
|
A | G | 1 | a0001c0005t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.572-163T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126400 | ||||||
chr6:4126413
|
G | A | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.572-176C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126413 | ||||||
chr6:4126467
|
A | C | 4 | a0001c0006t0002g0041a0001c0006t0005g0040a0006c0009t0001g0068others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.572-230T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126467 | ||||||
chr6:4126501
|
A | C | 1 | a0002c0002t0001g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.572-264T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126501 | ||||||
chr6:4126529
|
C | G | 83 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(80): Show | 207 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.572-292G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126529 | ||||||
chr6:4126682
|
G | A | 57 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(54): Show | 148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.572-445C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126682 | ||||||
chr6:4126701
|
G | A | 2 | a0006c0009t0001g0068a0006c0009t0002g0039 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.572-464C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126701 | ||||||
chr6:4126811
|
TTTAA | T | 1 | a0002c0002t0001g0012 | 5 | HG00558.hp2 NA18612.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.572-578_572-575del others(4): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126811 | ||||||
chr6:4126966
|
A | C | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.572-729T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126966 | ||||||
chr6:4126979
|
C | A | 2 | a0006c0009t0001g0068a0006c0009t0002g0039 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.572-742G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4126979 | ||||||
chr6:4127019
|
C | T | 57 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(54): Show | 148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.571+743G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127019 | ||||||
chr6:4127097
|
T | C | 4 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0075others(1): Show | 11 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.571+665A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127097 | ||||||
chr6:4127123
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.571+639G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127123 | ||||||
chr6:4127124
|
A | T | 1 | a0003c0003t0001g0113 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.571+638T>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127124 | ||||||
chr6:4127237
|
C | T | 2 | a0001c0006t0002g0041a0001c0006t0005g0040 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.571+525G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127237 | ||||||
chr6:4127387
|
G | A | 11 | a0002c0002t0001g0004a0002c0002t0001g0021a0002c0002t0001g0031others(8): Show | 31 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.571+375C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127387 | ||||||
chr6:4127404
|
C | CT | 21 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0033others(18): Show | 64 | HG00544.hp1 HG01167.hp1 HG01175.hp2 others(61): Show |
intron_variant | MODIFIER | c.571+357dupA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127404 | ||||||
chr6:4127404
|
C | CTT | 7 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0085others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.571+356_571+357dup others(2): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127404 | ||||||
chr6:4127404
|
CT | C | 27 | a0001c0001t0001g0101a0001c0001t0003g0052a0001c0006t0002g0018others(24): Show | 68 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.571+357delA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127404 | ||||||
chr6:4127404
|
CTT | C | 21 | a0002c0002t0001g0004a0002c0002t0001g0028a0002c0002t0001g0032others(18): Show | 58 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.571+356_571+357del others(2): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127404 | ||||||
chr6:4127404
|
CTTTTTTT others(4): Show |
C | 9 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(6): Show | 27 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.571+347_571+357del others(11): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127404 | ||||||
chr6:4127483
|
C | T | 2 | a0002c0002t0001g0124a0002c0002t0001g0126 | 2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.571+279G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127483 | ||||||
chr6:4127496
|
A | C | 57 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0009others(54): Show | 148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.571+266T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127496 | ||||||
chr6:4127546
|
C | A | 2 | a0002c0002t0001g0124a0002c0002t0001g0126 | 2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.571+216G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 5/9 | chr6 | 4127546 | ||||||
chr6:4127841
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0003g0051a0001c0001t0003g0052 | 3 | HG00741.hp2 HG01243.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.502-10C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4127841 | ||||||
chr6:4127847
|
A | G | 1 | a0002c0002t0001g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.502-16T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4127847 | ||||||
chr6:4127892
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.502-61C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4127892 | ||||||
chr6:4128079
|
T | C | 2 | a0006c0009t0001g0068a0006c0009t0002g0039 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.502-248A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4128079 | ||||||
chr6:4128209
|
A | G | 2 | a0001c0006t0002g0041a0001c0006t0005g0040 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.502-378T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4128209 | ||||||
chr6:4128506
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.502-675C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4128506 | ||||||
chr6:4128859
|
A | T | 2 | a0006c0009t0001g0068a0006c0009t0002g0039 | 2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.502-1028T>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4128859 | ||||||
chr6:4128886
|
G | A | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.502-1055C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4128886 | ||||||
chr6:4128971
|
T | C | 1 | a0003c0003t0001g0122 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.502-1140A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4128971 | ||||||
chr6:4129066
|
T | G | 1 | a0001c0001t0001g0104 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.502-1235A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129066 | ||||||
chr6:4129080
|
A | T | 2 | a0002c0002t0001g0124a0002c0002t0001g0126 | 2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.502-1249T>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129080 | ||||||
chr6:4129089
|
T | TCTCCCTC others(1): Show |
7 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0038others(4): Show | 13 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.502-1266_502-1259d others(10): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129089 | ||||||
chr6:4129289
|
T | A | 4 | a0001c0006t0002g0041a0001c0006t0005g0040a0006c0009t0001g0068others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+1083A>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129289 | ||||||
chr6:4129389
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.501+983G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129389 | ||||||
chr6:4129491
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.501+881T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129491 | ||||||
chr6:4129659
|
T | C | 1 | a0001c0001t0001g0029 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.501+713A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129659 | ||||||
chr6:4129685
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.501+687G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129685 | ||||||
chr6:4129702
|
G | T | 1 | a0003c0003t0001g0117 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.501+670C>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129702 | ||||||
chr6:4129897
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.501+475C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4129897 | ||||||
chr6:4130079
|
A | G | 27 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(24): Show | 60 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.501+293T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 4/9 | chr6 | 4130079 | ||||||
chr6:4130973
|
T | C | 4 | a0001c0006t0002g0041a0001c0006t0005g0040a0006c0009t0001g0068others(1): Show | 4 | HG02723.hp2 HG02970.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-108A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4130973 | ||||||
chr6:4131124
|
T | TA | 28 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(25): Show | 61 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(58): Show |
intron_variant | MODIFIER | c.214-260dupT | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131124 | ||||||
chr6:4131248
|
T | G | 27 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(24): Show | 60 | HG01074.hp1 HG01099.hp1 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.214-383A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131248 | ||||||
chr6:4131297
|
G | A | 2 | a0001c0001t0001g0070a0002c0002t0001g0069 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.214-432C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131297 | ||||||
chr6:4131412
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.214-547C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131412 | ||||||
chr6:4131424
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.214-559T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131424 | ||||||
chr6:4131477
|
A | G | 1 | a0001c0001t0001g0029 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.214-612T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131477 | ||||||
chr6:4131702
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.214-837G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131702 | ||||||
chr6:4131724
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(7): Show | 28 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.214-859C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131724 | ||||||
chr6:4131746
|
G | A | 27 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(24): Show | 59 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.214-881C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131746 | ||||||
chr6:4131875
|
CAAAAGAA | C | 59 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(56): Show | 156 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.214-1017_214-1011d others(9): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131875 | ||||||
chr6:4131900
|
G | C | 1 | a0001c0001t0001g0029 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.214-1035C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4131900 | ||||||
chr6:4132368
|
G | C | 25 | a0001c0001t0001g0029a0001c0001t0003g0051a0001c0001t0003g0052others(22): Show | 72 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.213+1181C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132368 | ||||||
chr6:4132417
|
A | G | 4 | a0001c0005t0001g0011a0001c0005t0001g0073a0001c0005t0001g0074others(1): Show | 9 | HG02257.hp1 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.213+1132T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132417 | ||||||
chr6:4132528
|
C | G | 37 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(34): Show | 89 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.213+1021G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132528 | ||||||
chr6:4132651
|
T | G | 1 | a0002c0002t0001g0053 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.213+898A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132651 | ||||||
chr6:4132752
|
ATC | A | 6 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0038others(3): Show | 12 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.213+795_213+796del others(2): Show |
ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132752 | ||||||
chr6:4132766
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.213+783A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132766 | ||||||
chr6:4132791
|
G | C | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.213+758C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132791 | ||||||
chr6:4132796
|
G | A | 10 | a0002c0002t0001g0004a0002c0002t0001g0021a0002c0002t0001g0031others(7): Show | 30 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.213+753C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132796 | ||||||
chr6:4132825
|
C | T | 1 | a0003c0003t0001g0116 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.213+724G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4132825 | ||||||
chr6:4133102
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.213+447G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133102 | ||||||
chr6:4133188
|
G | A | 1 | a0001c0001t0001g0036 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.213+361C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133188 | ||||||
chr6:4133199
|
G | A | 1 | a0001c0001t0001g0006 | 10 | HG01175.hp1 HG01975.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+350C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133199 | ||||||
chr6:4133257
|
T | C | 2 | a0002c0002t0001g0124a0002c0002t0001g0126 | 2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.213+292A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133257 | ||||||
chr6:4133263
|
G | C | 1 | a0002c0002t0001g0054 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.213+286C>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133263 | ||||||
chr6:4133313
|
A | G | 20 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(17): Show | 58 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.213+236T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133313 | ||||||
chr6:4133454
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.213+95T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133454 | ||||||
chr6:4133460
|
A | C | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.213+89T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133460 | ||||||
chr6:4133532
|
C | G | 20 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(17): Show | 58 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.213+17G>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 2/9 | chr6 | 4133532 | ||||||
chr6:4133719
|
T | C | 3 | a0001c0001t0001g0022a0002c0002t0001g0072a0007c0010t0001g0071 | 5 | HG02647.hp1 HG02965.hp2 HG03098.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.51-8A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4133719 | ||||||
chr6:4133797
|
A | C | 37 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(34): Show | 89 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.51-86T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4133797 | ||||||
chr6:4133807
|
AT | A | 8 | a0001c0004t0001g0013a0001c0004t0001g0014a0001c0004t0001g0075others(5): Show | 20 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.51-97delA | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4133807 | ||||||
chr6:4133813
|
G | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0033 | 6 | NA18949.hp1 NA18978.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.51-102C>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4133813 | ||||||
chr6:4133863
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.51-152A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4133863 | ||||||
chr6:4134012
|
A | C | 1 | a0003c0003t0001g0113 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.51-301T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134012 | ||||||
chr6:4134197
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.51-486C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134197 | ||||||
chr6:4134263
|
G | A | 37 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(34): Show | 89 | HG00280.hp2 HG01069.hp2 HG01070.hp2 others(86): Show |
intron_variant | MODIFIER | c.51-552C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134263 | ||||||
chr6:4134283
|
A | G | 1 | a0002c0002t0001g0078 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.51-572T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134283 | ||||||
chr6:4134347
|
C | T | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.51-636G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134347 | ||||||
chr6:4134534
|
A | G | 61 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0022others(58): Show | 159 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.51-823T>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134534 | ||||||
chr6:4134853
|
T | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | HG03688.hp2 HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.50+658A>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134853 | ||||||
chr6:4134862
|
A | C | 22 | a0001c0001t0003g0051a0001c0001t0003g0052a0002c0002t0001g0002others(19): Show | 68 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.50+649T>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134862 | ||||||
chr6:4134898
|
A | T | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.50+613T>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134898 | ||||||
chr6:4134991
|
C | A | 11 | a0001c0001t0001g0037a0001c0001t0001g0123a0003c0003t0001g0005others(8): Show | 29 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.50+520G>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4134991 | ||||||
chr6:4135028
|
T | C | 15 | a0001c0001t0001g0037a0001c0001t0001g0115a0001c0001t0001g0123others(12): Show | 35 | HG00140.hp2 HG00323.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.50+483A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4135028 | ||||||
chr6:4135085
|
T | G | 2 | a0002c0002t0001g0124a0002c0002t0001g0126 | 2 | HG02451.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.50+426A>C | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4135085 | ||||||
chr6:4135108
|
C | T | 24 | a0001c0001t0001g0029a0001c0001t0003g0051a0001c0001t0003g0052others(21): Show | 71 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.50+403G>A | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4135108 | ||||||
chr6:4135318
|
G | A | 1 | a0002c0002t0001g0125 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.50+193C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4135318 | ||||||
chr6:4135416
|
T | C | 1 | a0001c0006t0002g0018 | 3 | HG03516.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.50+95A>G | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4135416 | ||||||
chr6:4135426
|
G | A | 1 | a0002c0002t0001g0126 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.50+85C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4135426 | ||||||
chr6:4135482
|
G | A | 6 | a0002c0002t0001g0017a0002c0002t0001g0025a0002c0002t0001g0038others(3): Show | 12 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.50+29C>T | ECI2 | ENSG00000198721.13 | transcript | ENST00000380118.8 | protein_coding | 1/9 | chr6 | 4135482 |