Item | Value |
---|---|
geneid | 1894 |
ensemblid | ENSG00000114346.14 |
hgncid | 3155 |
symbol | ECT2 |
name | epithelial cell transforming 2 |
refseq_nuc | NM_001258315.2 |
refseq_prot | NP_001245244.1 |
ensembl_nuc | ENST00000392692.8 |
ensembl_prot | ENSP00000376457.3 |
mane_status | MANE Select |
chr | chr3 |
start | 172750726 |
end | 172821474 |
strand | + |
ver | v1.2 |
region | chr3:172750726-172821474 |
region5000 | chr3:172745726-172826474 |
regionname0 | ECT2_chr3_172750726_172821474 |
regionname5000 | ECT2_chr3_172745726_172826474 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 914 | 302 | 69 | 45 | 132 | 16 | 38 | 105 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0002 | 0/0 | 914 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0003 | 0/0 | 914 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0004 | 0/0 | 914 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0005 | 0/0 | 914 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0006 | 0/0 | 914 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0007 | 0/0 | 914 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0008 | 0/0 | 914 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2745 | 292 | 63 | 41 | 132 | 16 | 38 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
c0002 | 0/0 | 2745 | 7 | 5 | 2 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
c0003 | 0/0 | 2745 | 6 | 6 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
c0004 | 0/0 | 2745 | 4 | 4 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
c0005 | 0/0 | 2745 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
c0006 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
c0007 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
c0008 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
c0009 | 0/0 | 2745 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
c0010 | 0/0 | 2745 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
c0011 | 0/0 | 2745 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
c0012 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1392 | 123 | 40 | 20 | 38 | 8 | 15 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
t0002 | 0/0 | 1392 | 100 | 5 | 18 | 59 | 6 | 12 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
t0003 | 0/0 | 1392 | 46 | 8 | 0 | 33 | 1 | 4 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
t0004 | 0/0 | 1392 | 24 | 23 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
t0005 | 0/0 | 1392 | 5 | 0 | 3 | 0 | 0 | 2 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
t0006 | 0/0 | 1392 | 5 | 0 | 2 | 1 | 1 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
t0007 | 0/0 | 1392 | 5 | 1 | 1 | 0 | 0 | 3 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
t0008 | 0/0 | 1392 | 4 | 4 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
t0009 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
t0010 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
t0011 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
t0012 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
t0013 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
t0014 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0003 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0004 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0005 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0032 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2745 | 292 | 63 | 41 | 132 | 16 | 38 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
a0001c0002 | 0/0 | 2745 | 7 | 5 | 2 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
a0001c0006 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
a0001c0009 | 0/0 | 2745 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
a0001c0010 | 0/0 | 2745 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
a0002c0003 | 0/0 | 2745 | 6 | 6 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
a0003c0004 | 0/0 | 2745 | 4 | 4 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
a0004c0005 | 0/0 | 2745 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
a0005c0007 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
a0006c0008 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
a0007c0011 | 0/0 | 2745 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 | |
a0008c0012 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4136 | 114 | 34 | 17 | 38 | 8 | 15 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0001t0002 | 0/0 | 4136 | 97 | 5 | 16 | 58 | 6 | 12 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0001t0003 | 0/0 | 4136 | 39 | 2 | 0 | 32 | 1 | 4 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0001t0004 | 0/0 | 4136 | 21 | 20 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0001t0005 | 0/0 | 4136 | 5 | 0 | 3 | 0 | 0 | 2 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0001t0006 | 0/0 | 4136 | 5 | 0 | 2 | 1 | 1 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0001t0007 | 0/0 | 4136 | 5 | 1 | 1 | 0 | 0 | 3 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0001t0009 | 0/0 | 4136 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0001t0010 | 0/0 | 4136 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0001t0011 | 0/0 | 4136 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0001t0012 | 0/0 | 4136 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0001t0013 | 0/0 | 4136 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0001t0014 | 0/0 | 4136 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0002t0001 | 0/0 | 4136 | 7 | 5 | 2 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0006t0004 | 0/0 | 4136 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0009t0002 | 0/0 | 4136 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0001c0010t0001 | 0/0 | 4136 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0002c0003t0003 | 0/0 | 4136 | 6 | 6 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0003c0004t0008 | 0/0 | 4136 | 4 | 4 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0004c0005t0004 | 0/0 | 4136 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0005c0007t0002 | 0/0 | 4136 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0006c0008t0001 | 0/0 | 4136 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0007c0011t0002 | 0/0 | 4136 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
a0008c0012t0003 | 0/0 | 4136 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | copy fasta | chr3 | 172745726 | 172826474 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0032 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0004 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0007g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0007g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0009g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0010g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0011g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0012g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0013g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0001t0014g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0002t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0006t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0009t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0001c0010t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0002c0003t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0002c0003t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0002c0003t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0002c0003t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0002c0003t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0003c0004t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0003c0004t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0003c0004t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0003c0004t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0004c0005t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0004c0005t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0005c0007t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0006c0008t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0007c0011t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
a0008c0012t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0131 | EUR | GBR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0168 | EUR | GBR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0173 | EUR | FIN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | CHS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | CHS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | CHS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | CHS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00735 | hp2 | a0001 | c0010 | t0001 | g0037 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0123 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0145 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01109 | hp1 | a0007 | c0011 | t0002 | g0174 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01192 | hp2 | a0001 | c0001 | t0007 | g0019 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01243 | hp1 | a0001 | c0009 | t0002 | g0172 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0253 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0202 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0209 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01361 | hp2 | a0001 | c0001 | t0010 | g0210 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0160 | EUR | IBS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0124 | EUR | IBS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01884 | hp1 | a0003 | c0004 | t0008 | g0112 | AFR | ACB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | ACB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PEL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02071 | hp1 | a0001 | c0001 | t0013 | g0122 | EAS | KHV | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | KHV | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02165 | hp2 | a0008 | c0012 | t0003 | g0221 | EAS | CDX | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02257 | hp2 | a0002 | c0003 | t0003 | g0094 | AFR | ACB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02293 | hp2 | a0001 | c0001 | t0006 | g0142 | AMR | PEL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | KHV | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0262 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02615 | hp2 | a0002 | c0003 | t0003 | g0095 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02622 | hp2 | a0002 | c0003 | t0003 | g0022 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0245 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02717 | hp2 | a0004 | c0005 | t0004 | g0256 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02723 | hp2 | a0003 | c0004 | t0008 | g0113 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02735 | hp1 | a0001 | c0001 | t0009 | g0060 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0198 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0250 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0263 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0261 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0254 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03041 | hp2 | a0002 | c0003 | t0003 | g0022 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03098 | hp1 | a0002 | c0003 | t0003 | g0096 | AFR | MSL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | MSL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03130 | hp1 | a0003 | c0004 | t0008 | g0114 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0246 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | MSL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | MSL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0247 | AFR | MSL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0171 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03516 | hp2 | a0002 | c0003 | t0003 | g0097 | AFR | ESN | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0255 | AFR | MSL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03579 | hp2 | a0001 | c0001 | t0011 | g0196 | AFR | MSL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0215 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03688 | hp1 | a0001 | c0001 | t0007 | g0098 | SAS | STU | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | STU | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03710 | hp1 | a0001 | c0001 | t0007 | g0084 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | BEB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | BEB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | BEB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0238 | SAS | BEB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0226 | SAS | STU | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0229 | SAS | STU | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0083 | SAS | STU | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG04228 | hp2 | a0001 | c0001 | t0005 | g0117 | SAS | STU | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | YRI | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18957 | hp2 | a0001 | c0001 | t0006 | g0178 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18959 | hp1 | a0005 | c0007 | t0002 | g0004 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18965 | hp2 | a0001 | c0001 | t0012 | g0130 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18994 | hp2 | a0001 | c0001 | t0014 | g0149 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19030 | hp2 | a0001 | c0006 | t0004 | g0251 | AFR | LWK | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19072 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | YRI | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | YRI | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0248 | AFR | ASW | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0129 | EUR | TSI | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | TSI | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0240 | EUR | TSI | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | GIH | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | GIH | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0252 | AFR | ACB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02559 | hp1 | a0006 | c0008 | t0001 | g0076 | AFR | ACB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | USA | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | USA | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA20300 | hp1 | a0004 | c0005 | t0004 | g0257 | AFR | USA | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA20300 | hp2 | a0003 | c0004 | t0008 | g0111 | AFR | USA | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0019 | AFR | LWK | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | LWK | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0032 | REF | REF | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0078 | REF | REF | ECT2_chr3_172745726_172826474 | ECT2 | chr3 | 172745726 | 172826474 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:172754574 | G | C | 1 | a0003 | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
missense_variant | MODERATE | c.44G>C | p.Ser15Thr | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 2/25 | 198/4136 | 44/2745 | 15/914 | chr3 | 172754574 | ||
chr3:172754610 | C | T | 1 | a0004 | 2 | HG02717.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.80C>T | p.Thr27Ile | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 2/25 | 234/4136 | 80/2745 | 27/914 | chr3 | 172754610 | ||
chr3:172755507 | G | A | 1 | a0002 | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
missense_variant | MODERATE | c.235G>A | p.Val79Ile | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/25 | 389/4136 | 235/2745 | 79/914 | chr3 | 172755507 | ||
chr3:172755573 | A | G | 1 | a0008 | 1 | HG02165.hp2 | missense_variant&splice_region_variant | MODERATE | c.301A>G | p.Met101Val | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/25 | 455/4136 | 301/2745 | 101/914 | chr3 | 172755573 | ||
chr3:172762732 | C | G | 1 | a0007 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.931C>G | p.Leu311Val | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 10/25 | 1085/4136 | 931/2745 | 311/914 | chr3 | 172762732 | ||
chr3:172786574 | C | T | 2 | a0005a0006 | 2 | HG02559.hp1 NA18959.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1907C>T | p.Thr636Met | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/25 | 2061/4136 | 1907/2745 | 636/914 | chr3 | 172786574 | ||
chr3:172816692 | T | A | 1 | a0005 | 1 | NA18959.hp1 | missense_variant&splice_region_variant | MODERATE | c.2510T>A | p.Val837Asp | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/25 | 2664/4136 | 2510/2745 | 837/914 | chr3 | 172816692 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:172755327 | T | C | 1 | a0001c0006 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.163T>C | p.Leu55Leu | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 3/25 | 317/4136 | 163/2745 | 55/914 | chr3 | 172755327 | ||
chr3:172764322 | A | G | 1 | a0001c0010 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.1113A>G | p.Leu371Leu | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/25 | 1267/4136 | 1113/2745 | 371/914 | chr3 | 172764322 | ||
chr3:172773917 | A | G | 1 | a0001c0002 | 7 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(4): Show |
synonymous_variant | LOW | c.1443A>G | p.Pro481Pro | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/25 | 1597/4136 | 1443/2745 | 481/914 | chr3 | 172773917 | ||
chr3:172773918 | T | C | 1 | a0002c0003 | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
synonymous_variant | LOW | c.1444T>C | p.Leu482Leu | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/25 | 1598/4136 | 1444/2745 | 482/914 | chr3 | 172773918 | ||
chr3:172784766 | A | G | 1 | a0001c0009 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1788A>G | p.Pro596Pro | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/25 | 1942/4136 | 1788/2745 | 596/914 | chr3 | 172784766 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:172750768 | G | T | 1 | a0001c0001t0014 | 1 | NA18994.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-112G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/25 | chr3 | 172750768 | ||||||
chr3:172820250 | A | T | 1 | a0001c0001t0007 | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*13A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 25/25 | 13 | chr3 | 172820250 | |||||
chr3:172820275 | C | T | 1 | a0001c0001t0006 | 5 | HG00741.hp2 HG01517.hp1 HG02293.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*38C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 25/25 | 38 | chr3 | 172820275 | |||||
chr3:172820407 | T | C | 1 | a0003c0004t0008 | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*170T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 25/25 | 170 | chr3 | 172820407 | |||||
chr3:172820560 | C | T | 9 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(6): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*323C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 25/25 | 323 | chr3 | 172820560 | |||||
chr3:172820601 | A | G | 2 | a0001c0001t0005a0001c0001t0011 | 6 | HG01074.hp1 HG01261.hp2 HG01358.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*364A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 25/25 | 364 | chr3 | 172820601 | |||||
chr3:172820630 | T | A | 1 | a0001c0001t0012 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 25/25 | 393 | chr3 | 172820630 | |||||
chr3:172820836 | A | C | 1 | a0001c0001t0007 | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*599A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 25/25 | 599 | chr3 | 172820836 | |||||
chr3:172820923 | A | T | 1 | a0001c0001t0010 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*686A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 25/25 | 686 | chr3 | 172820923 | |||||
chr3:172820965 | A | G | 6 | a0001c0001t0003a0001c0001t0004a0001c0006t0004others(3): Show | 70 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*728A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 25/25 | 728 | chr3 | 172820965 | |||||
chr3:172821001 | A | C | 1 | a0001c0001t0009 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*764A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 25/25 | 764 | chr3 | 172821001 | |||||
chr3:172821092 | A | G | 3 | a0001c0001t0004a0001c0006t0004a0004c0005t0004 | 24 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*855A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 25/25 | 855 | chr3 | 172821092 | |||||
chr3:172821204 | A | T | 1 | a0001c0001t0013 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*967A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 25/25 | 967 | chr3 | 172821204 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:172750867 | C | T | 1 | a0001c0001t0003g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-23+10C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172750867 | ||||||
chr3:172751090 | C | G | 1 | a0001c0001t0002g0264 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-23+233C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172751090 | ||||||
chr3:172751246 | C | T | 1 | a0001c0001t0001g0010 | 3 | HG02109.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+389C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172751246 | ||||||
chr3:172751403 | C | T | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.-23+546C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172751403 | ||||||
chr3:172751479 | A | G | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.-23+622A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172751479 | ||||||
chr3:172751575 | T | TAGTAATG others(324): Show |
1 | a0001c0001t0001g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-23+733_-23+734ins others(331): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr3 | 172751575 | |||||
chr3:172751636 | T | C | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.-23+779T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172751636 | ||||||
chr3:172751732 | T | TTA | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.-23+878_-23+879dup others(2): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr3 | 172751732 | |||||
chr3:172751803 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.-23+946G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172751803 | ||||||
chr3:172751844 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-23+987A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172751844 | ||||||
chr3:172752157 | C | CTACCTCT others(3): Show |
1 | a0001c0001t0002g0211 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-23+1306_-23+1315d others(12): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr3 | 172752157 | |||||
chr3:172752310 | A | G | 1 | a0001c0001t0010g0210 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-23+1453A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172752310 | ||||||
chr3:172752318 | C | T | 101 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(98): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-23+1461C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172752318 | ||||||
chr3:172752454 | C | T | 1 | a0001c0001t0005g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-23+1597C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172752454 | ||||||
chr3:172752505 | A | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-23+1648A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172752505 | ||||||
chr3:172752554 | C | T | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+1697C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172752554 | ||||||
chr3:172752574 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-23+1717A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172752574 | ||||||
chr3:172752605 | T | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 20 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.-23+1748T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172752605 | ||||||
chr3:172752633 | T | TA | 3 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044 | 5 | HG02109.hp2 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+1777dupA | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr3 | 172752633 | |||||
chr3:172752767 | T | G | 1 | a0001c0001t0005g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-22-1742T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172752767 | ||||||
chr3:172752846 | A | G | 1 | a0001c0001t0004g0263 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-22-1663A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172752846 | ||||||
chr3:172752943 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-22-1566A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172752943 | ||||||
chr3:172752966 | C | T | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-1543C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172752966 | ||||||
chr3:172753180 | A | G | 1 | a0001c0001t0001g0025 | 2 | NA18977.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.-22-1329A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172753180 | ||||||
chr3:172753190 | C | A | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-1319C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172753190 | ||||||
chr3:172753312 | G | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(11): Show | 20 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.-22-1197G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172753312 | ||||||
chr3:172753329 | C | T | 1 | a0001c0001t0004g0262 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-22-1180C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172753329 | ||||||
chr3:172753515 | G | A | 4 | a0001c0002t0001g0014a0001c0002t0001g0045a0001c0002t0001g0046others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-994G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172753515 | ||||||
chr3:172753526 | T | C | 101 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(98): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.-22-983T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172753526 | ||||||
chr3:172753527 | T | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.-22-982T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172753527 | ||||||
chr3:172753569 | A | C | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-940A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172753569 | ||||||
chr3:172753633 | T | A | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-876T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172753633 | ||||||
chr3:172753689 | A | G | 1 | a0001c0001t0002g0208 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-22-820A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172753689 | ||||||
chr3:172753813 | C | T | 1 | a0001c0001t0002g0207 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-22-696C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172753813 | ||||||
chr3:172753902 | T | C | 1 | a0001c0001t0003g0214 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-22-607T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172753902 | ||||||
chr3:172754001 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.-22-508G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172754001 | ||||||
chr3:172754107 | A | C | 2 | a0001c0001t0004g0107a0001c0001t0004g0108 | 2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-22-402A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172754107 | ||||||
chr3:172754150 | G | A | 1 | a0001c0001t0004g0244 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-22-359G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172754150 | ||||||
chr3:172754305 | A | G | 1 | a0001c0001t0004g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-22-204A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172754305 | ||||||
chr3:172754323 | A | G | 1 | a0001c0001t0004g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-22-186A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 1/24 | chr3 | 172754323 | ||||||
chr3:172754941 | A | G | 43 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044others(40): Show | 52 | HG00621.hp2 HG00673.hp1 HG02109.hp2 others(49): Show |
intron_variant | MODIFIER | c.130+281A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 2/24 | chr3 | 172754941 | ||||||
chr3:172754972 | T | C | 1 | a0001c0001t0003g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.130+312T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 2/24 | chr3 | 172754972 | ||||||
chr3:172755184 | T | C | 2 | a0001c0001t0002g0118a0001c0001t0002g0119 | 2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.131-111T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 2/24 | chr3 | 172755184 | ||||||
chr3:172755203 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.131-92A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 2/24 | chr3 | 172755203 | ||||||
chr3:172755229 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.131-66C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 2/24 | chr3 | 172755229 | ||||||
chr3:172755269 | C | CAT | 64 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044others(61): Show | 74 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(71): Show |
intron_variant | MODIFIER | c.131-25_131-24dupAT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr3 | 172755269 | |||||
chr3:172755404 | G | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0048others(4): Show | 9 | HG01433.hp2 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.210+30G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 3/24 | chr3 | 172755404 | ||||||
chr3:172755459 | C | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0087others(5): Show | 10 | HG01884.hp2 HG02257.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.211-24C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 3/24 | chr3 | 172755459 | ||||||
chr3:172755694 | A | G | 106 | a0001c0001t0001g0086a0001c0001t0002g0001a0001c0001t0002g0004others(103): Show | 118 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.303+119A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172755694 | ||||||
chr3:172755794 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.303+219G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172755794 | ||||||
chr3:172755866 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.303+291G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172755866 | ||||||
chr3:172755922 | C | A | 1 | a0001c0001t0004g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.303+347C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172755922 | ||||||
chr3:172755967 | T | A | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.303+392T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172755967 | ||||||
chr3:172756078 | G | A | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.303+503G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172756078 | ||||||
chr3:172756132 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.303+557C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172756132 | ||||||
chr3:172756297 | A | G | 106 | a0001c0001t0001g0086a0001c0001t0002g0001a0001c0001t0002g0004others(103): Show | 118 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.304-686A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172756297 | ||||||
chr3:172756299 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.304-684A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172756299 | ||||||
chr3:172756300 | T | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 20 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.304-683T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172756300 | ||||||
chr3:172756320 | G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0087 | 3 | HG02717.hp1 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.304-663G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172756320 | ||||||
chr3:172756339 | G | T | 1 | a0001c0001t0002g0205 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.304-644G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172756339 | ||||||
chr3:172756346 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.304-637T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172756346 | ||||||
chr3:172756366 | G | T | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-617G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172756366 | ||||||
chr3:172756486 | A | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0048others(4): Show | 9 | HG01433.hp2 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-497A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172756486 | ||||||
chr3:172756566 | A | G | 1 | a0001c0001t0002g0204 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.304-417A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172756566 | ||||||
chr3:172756622 | A | G | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.304-361A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172756622 | ||||||
chr3:172756712 | A | T | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-271A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172756712 | ||||||
chr3:172756725 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.304-258A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 4/24 | chr3 | 172756725 | ||||||
chr3:172757385 | A | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0048others(4): Show | 9 | HG01433.hp2 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.486+220A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172757385 | ||||||
chr3:172757415 | C | CT | 117 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0093others(114): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.486+269dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172757415 | |||||
chr3:172757415 | C | CTT | 8 | a0001c0001t0002g0197a0001c0001t0002g0199a0001c0001t0002g0200others(5): Show | 8 | HG01261.hp2 HG02738.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.486+268_486+269dup others(2): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172757415 | |||||
chr3:172757440 | G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044 | 5 | HG02109.hp2 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.486+275G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172757440 | ||||||
chr3:172757479 | G | C | 1 | a0001c0001t0001g0031 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.486+314G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172757479 | ||||||
chr3:172757517 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.486+352G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172757517 | ||||||
chr3:172757603 | G | C | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+438G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172757603 | ||||||
chr3:172757623 | G | A | 5 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0045others(2): Show | 7 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.486+458G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172757623 | ||||||
chr3:172757664 | T | C | 169 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044others(166): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.486+499T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172757664 | ||||||
chr3:172757713 | C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | NA18950.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.486+548C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172757713 | ||||||
chr3:172757830 | G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044 | 5 | HG02109.hp2 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.486+665G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172757830 | ||||||
chr3:172757833 | C | G | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.486+668C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172757833 | ||||||
chr3:172757864 | T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044 | 5 | HG02109.hp2 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.486+699T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172757864 | ||||||
chr3:172757887 | G | GTATT | 32 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(29): Show | 38 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(35): Show |
intron_variant | MODIFIER | c.486+737_486+740dup others(4): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172757887 | |||||
chr3:172757950 | C | T | 1 | a0001c0001t0003g0216 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.486+785C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172757950 | ||||||
chr3:172758194 | C | T | 1 | a0001c0001t0005g0202 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.487-786C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172758194 | ||||||
chr3:172758243 | A | G | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.487-737A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172758243 | ||||||
chr3:172758254 | G | A | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.487-726G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172758254 | ||||||
chr3:172758378 | A | G | 19 | a0001c0001t0004g0030a0001c0001t0004g0245a0001c0001t0004g0246others(16): Show | 20 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.487-602A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172758378 | ||||||
chr3:172758456 | C | T | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.487-524C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172758456 | ||||||
chr3:172758468 | T | TACAC | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 27 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.487-498_487-495dup others(4): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172758468 | |||||
chr3:172758468 | T | TACACAC | 157 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(154): Show | 188 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.487-500_487-495dup others(6): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172758468 | |||||
chr3:172758468 | T | TACACACA others(1): Show |
20 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0023others(17): Show | 29 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.487-502_487-495dup others(8): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172758468 | |||||
chr3:172758468 | T | TACACACA others(3): Show |
2 | a0001c0001t0004g0107a0001c0001t0004g0108 | 2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.487-504_487-495dup others(10): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172758468 | |||||
chr3:172758468 | T | TACACACA others(5): Show |
1 | a0001c0001t0003g0242 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.487-506_487-495dup others(12): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172758468 | |||||
chr3:172758468 | T | TACACACA others(7): Show |
15 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0249others(12): Show | 16 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.487-508_487-495dup others(14): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172758468 | |||||
chr3:172758468 | T | TACACACA others(9): Show |
6 | a0001c0001t0003g0241a0001c0001t0004g0245a0001c0001t0004g0246others(3): Show | 6 | HG02132.hp2 HG02630.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-510_487-495dup others(16): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172758468 | |||||
chr3:172758468 | T | TACACACA others(11): Show |
29 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0214others(26): Show | 34 | HG00621.hp2 HG00673.hp1 HG02165.hp2 others(31): Show |
intron_variant | MODIFIER | c.487-495_487-494ins others(18): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172758468 | |||||
chr3:172758468 | T | TACACACA others(13): Show |
3 | a0001c0001t0003g0029a0001c0001t0003g0217a0001c0001t0003g0218 | 4 | NA18968.hp1 NA18993.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-495_487-494ins others(20): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172758468 | |||||
chr3:172758470 | CACACACA others(9): Show |
C | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-494_487-479del others(16): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172758470 | |||||
chr3:172758486 | G | C | 1 | a0001c0001t0004g0248 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.487-494G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172758486 | ||||||
chr3:172758490 | C | CACACACA others(3): Show |
1 | a0001c0001t0004g0248 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.487-481_487-480ins others(10): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172758490 | |||||
chr3:172758501 | A | AACC | 2 | a0001c0001t0001g0010a0001c0001t0001g0043 | 4 | HG02109.hp2 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-478_487-476dup others(3): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr3 | 172758501 | |||||
chr3:172758629 | G | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.487-351G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172758629 | ||||||
chr3:172758782 | C | T | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.487-198C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 5/24 | chr3 | 172758782 | ||||||
chr3:172759081 | G | A | 2 | a0001c0001t0002g0026a0001c0001t0013g0122 | 3 | HG02071.hp1 NA18969.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.576+12G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172759081 | ||||||
chr3:172759107 | C | T | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+38C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172759107 | ||||||
chr3:172759223 | A | G | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.576+154A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172759223 | ||||||
chr3:172759365 | T | C | 2 | a0001c0001t0006g0123a0001c0001t0006g0124 | 2 | HG00741.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.576+296T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172759365 | ||||||
chr3:172759415 | T | G | 169 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044others(166): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.576+346T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172759415 | ||||||
chr3:172759532 | C | T | 2 | a0004c0005t0004g0256a0004c0005t0004g0257 | 2 | HG02717.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.576+463C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172759532 | ||||||
chr3:172759570 | G | C | 200 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(197): Show | 233 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.576+501G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172759570 | ||||||
chr3:172759612 | T | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.576+543T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172759612 | ||||||
chr3:172759687 | G | A | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.577-469G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172759687 | ||||||
chr3:172759800 | C | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0048others(4): Show | 9 | HG01433.hp2 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.577-356C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172759800 | ||||||
chr3:172759862 | A | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.577-294A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172759862 | ||||||
chr3:172759902 | A | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 4 | NA18947.hp2 NA18965.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-254A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172759902 | ||||||
chr3:172759949 | A | T | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.577-207A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172759949 | ||||||
chr3:172760085 | T | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.577-71T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172760085 | ||||||
chr3:172760090 | T | C | 1 | a0001c0001t0005g0202 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.577-66T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 6/24 | chr3 | 172760090 | ||||||
chr3:172760289 | T | G | 1 | a0001c0001t0003g0214 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.684+26T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | chr3 | 172760289 | ||||||
chr3:172760296 | A | G | 1 | a0001c0001t0002g0201 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.684+33A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | chr3 | 172760296 | ||||||
chr3:172760357 | TAAAG | T | 26 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(23): Show | 29 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.684+97_684+100delA others(3): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr3 | 172760357 | |||||
chr3:172760432 | CTTTCT | C | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+188_684+192del others(5): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr3 | 172760432 | |||||
chr3:172760461 | A | T | 20 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(17): Show | 21 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.684+198A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | chr3 | 172760461 | ||||||
chr3:172760712 | C | CT | 39 | a0001c0001t0001g0038a0001c0001t0001g0072a0001c0001t0001g0073others(36): Show | 39 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.684+475dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr3 | 172760712 | |||||
chr3:172760712 | C | CTT | 26 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0048others(23): Show | 33 | HG01433.hp2 HG01891.hp1 HG02132.hp2 others(30): Show |
intron_variant | MODIFIER | c.684+474_684+475dup others(2): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr3 | 172760712 | |||||
chr3:172760712 | C | CTTT | 13 | a0001c0001t0001g0052a0001c0001t0003g0029a0001c0001t0003g0231others(10): Show | 14 | HG00621.hp2 HG00673.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.684+473_684+475dup others(3): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr3 | 172760712 | |||||
chr3:172760712 | CT | C | 20 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0086others(17): Show | 27 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.684+475delT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr3 | 172760712 | |||||
chr3:172760712 | CTTTT | C | 14 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(11): Show | 15 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.684+472_684+475del others(4): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr3 | 172760712 | |||||
chr3:172760738 | T | TTG | 4 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 6 | HG02109.hp2 HG02965.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+475_684+476ins others(2): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | chr3 | 172760738 | ||||||
chr3:172760815 | G | A | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+552G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | chr3 | 172760815 | ||||||
chr3:172760889 | T | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0025others(13): Show | 24 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.684+626T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | chr3 | 172760889 | ||||||
chr3:172761014 | C | A | 2 | a0001c0001t0002g0027a0001c0001t0002g0183 | 3 | NA18947.hp1 NA18983.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.685-596C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | chr3 | 172761014 | ||||||
chr3:172761083 | G | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 20 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.685-527G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | chr3 | 172761083 | ||||||
chr3:172761185 | C | T | 1 | a0001c0001t0002g0182 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.685-425C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | chr3 | 172761185 | ||||||
chr3:172761333 | C | T | 5 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0045others(2): Show | 7 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.685-277C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | chr3 | 172761333 | ||||||
chr3:172761334 | G | A | 101 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(98): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.685-276G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | chr3 | 172761334 | ||||||
chr3:172761360 | A | G | 13 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(10): Show | 19 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.685-250A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 7/24 | chr3 | 172761360 | ||||||
chr3:172761699 | C | T | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.758+16C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 8/24 | chr3 | 172761699 | ||||||
chr3:172762057 | C | T | 105 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(102): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.759-359C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 8/24 | chr3 | 172762057 | ||||||
chr3:172762083 | A | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.759-333A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 8/24 | chr3 | 172762083 | ||||||
chr3:172762113 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.759-303A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 8/24 | chr3 | 172762113 | ||||||
chr3:172762173 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.759-243A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 8/24 | chr3 | 172762173 | ||||||
chr3:172762383 | A | AT | 101 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(98): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.759-33_759-32insT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 8/24 | chr3 | 172762383 | ||||||
chr3:172762384 | A | T | 101 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(98): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.759-32A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 8/24 | chr3 | 172762384 | ||||||
chr3:172762385 | C | A | 101 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(98): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.759-31C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 8/24 | chr3 | 172762385 | ||||||
chr3:172763057 | T | C | 1 | a0001c0001t0003g0220 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1068+85T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 11/24 | chr3 | 172763057 | ||||||
chr3:172763102 | A | T | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1068+130A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 11/24 | chr3 | 172763102 | ||||||
chr3:172763232 | A | T | 100 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(97): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1068+260A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 11/24 | chr3 | 172763232 | ||||||
chr3:172763270 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1068+298G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 11/24 | chr3 | 172763270 | ||||||
chr3:172763352 | G | A | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.1068+380G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 11/24 | chr3 | 172763352 | ||||||
chr3:172763456 | A | G | 5 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0045others(2): Show | 7 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1068+484A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 11/24 | chr3 | 172763456 | ||||||
chr3:172763541 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1068+569C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 11/24 | chr3 | 172763541 | ||||||
chr3:172763554 | G | C | 2 | a0001c0001t0002g0128a0001c0001t0002g0129 | 2 | HG01169.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1068+582G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 11/24 | chr3 | 172763554 | ||||||
chr3:172763739 | C | T | 1 | a0001c0001t0002g0181 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1069-539C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 11/24 | chr3 | 172763739 | ||||||
chr3:172763831 | G | T | 58 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044others(55): Show | 67 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(64): Show |
intron_variant | MODIFIER | c.1069-447G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 11/24 | chr3 | 172763831 | ||||||
chr3:172764105 | G | A | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.1069-173G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 11/24 | chr3 | 172764105 | ||||||
chr3:172764111 | T | C | 23 | a0001c0001t0004g0030a0001c0001t0004g0107a0001c0001t0004g0108others(20): Show | 24 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(21): Show |
intron_variant | MODIFIER | c.1069-167T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 11/24 | chr3 | 172764111 | ||||||
chr3:172764235 | A | C | 1 | a0001c0001t0003g0240 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1069-43A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 11/24 | chr3 | 172764235 | ||||||
chr3:172764705 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1291+205C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172764705 | ||||||
chr3:172764963 | CCTTT | C | 7 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0001g0102others(4): Show | 8 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291+468_1291+471d others(6): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr3 | 172764963 | |||||
chr3:172765028 | A | C | 1 | a0003c0004t0008g0114 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1291+528A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172765028 | ||||||
chr3:172765240 | C | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1291+740C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172765240 | ||||||
chr3:172765318 | A | G | 20 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(17): Show | 21 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.1291+818A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172765318 | ||||||
chr3:172765391 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1291+891A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172765391 | ||||||
chr3:172765643 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1291+1143C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172765643 | ||||||
chr3:172765658 | C | T | 1 | a0001c0001t0001g0013 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1291+1158C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172765658 | ||||||
chr3:172765920 | G | A | 1 | a0001c0001t0007g0098 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1291+1420G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172765920 | ||||||
chr3:172766090 | T | C | 1 | a0001c0001t0002g0125 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1291+1590T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172766090 | ||||||
chr3:172766113 | C | T | 5 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0045others(2): Show | 7 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1291+1613C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172766113 | ||||||
chr3:172766152 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1291+1652G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172766152 | ||||||
chr3:172766516 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1291+2016G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172766516 | ||||||
chr3:172766530 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1291+2030A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172766530 | ||||||
chr3:172766627 | A | G | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291+2127A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172766627 | ||||||
chr3:172766707 | G | A | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291+2207G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172766707 | ||||||
chr3:172766792 | A | G | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-2215A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172766792 | ||||||
chr3:172766869 | G | T | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1292-2138G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172766869 | ||||||
chr3:172766899 | CAA | C | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(15): Show | 21 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1292-2107_1292-210 others(6): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172766899 | ||||||
chr3:172766911 | A | G | 2 | a0001c0001t0004g0107a0001c0001t0004g0108 | 2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1292-2096A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172766911 | ||||||
chr3:172767147 | A | T | 1 | a0001c0001t0001g0041 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1292-1860A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172767147 | ||||||
chr3:172767152 | G | C | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(15): Show | 21 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1292-1855G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172767152 | ||||||
chr3:172767168 | C | T | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1292-1839C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172767168 | ||||||
chr3:172767459 | A | T | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1292-1548A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172767459 | ||||||
chr3:172767593 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1292-1414G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172767593 | ||||||
chr3:172767683 | A | G | 1 | a0001c0001t0004g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1292-1324A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172767683 | ||||||
chr3:172767724 | A | ATTTTTTT others(4): Show |
19 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(16): Show | 20 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.1292-1273_1292-127 others(15): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr3 | 172767724 | |||||
chr3:172767724 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0004g0258a0001c0001t0004g0259 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1292-1273_1292-127 others(16): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr3 | 172767724 | |||||
chr3:172767769 | G | C | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.1292-1238G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172767769 | ||||||
chr3:172767771 | G | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1292-1236G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172767771 | ||||||
chr3:172767781 | G | A | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1292-1226G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172767781 | ||||||
chr3:172767846 | C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070 | 3 | HG02080.hp1 HG02155.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1292-1161C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172767846 | ||||||
chr3:172768032 | G | A | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1292-975G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172768032 | ||||||
chr3:172768061 | T | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1292-946T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172768061 | ||||||
chr3:172768158 | G | GT | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1292-843dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr3 | 172768158 | |||||
chr3:172768577 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1292-430G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172768577 | ||||||
chr3:172768741 | T | A | 1 | a0001c0001t0001g0053 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1292-266T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172768741 | ||||||
chr3:172768807 | T | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(10): Show | 19 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1292-200T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172768807 | ||||||
chr3:172769000 | G | A | 1 | a0001c0001t0012g0130 | 1 | NA18965.hp2 | splice_region_variant&intron_variant | LOW | c.1292-7G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 12/24 | chr3 | 172769000 | ||||||
chr3:172769174 | C | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0099others(2): Show | 10 | HG01070.hp2 HG01109.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1428+31C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172769174 | ||||||
chr3:172769223 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1428+80G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172769223 | ||||||
chr3:172769244 | T | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1428+101T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172769244 | ||||||
chr3:172769381 | G | A | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.1428+238G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172769381 | ||||||
chr3:172769540 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1428+397G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172769540 | ||||||
chr3:172770045 | C | A | 1 | a0001c0001t0001g0015 | 2 | HG01891.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1428+902C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172770045 | ||||||
chr3:172770069 | A | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1428+926A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172770069 | ||||||
chr3:172770194 | G | T | 19 | a0001c0001t0004g0030a0001c0001t0004g0245a0001c0001t0004g0246others(16): Show | 20 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.1428+1051G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172770194 | ||||||
chr3:172770283 | G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0099others(2): Show | 10 | HG01070.hp2 HG01109.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1428+1140G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172770283 | ||||||
chr3:172770489 | A | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1428+1346A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172770489 | ||||||
chr3:172770502 | C | T | 60 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(57): Show | 68 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(65): Show |
intron_variant | MODIFIER | c.1428+1359C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172770502 | ||||||
chr3:172770511 | A | T | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1428+1368A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172770511 | ||||||
chr3:172770565 | T | C | 165 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(162): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1428+1422T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172770565 | ||||||
chr3:172770584 | C | T | 101 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(98): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1428+1441C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172770584 | ||||||
chr3:172770679 | G | T | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1428+1536G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172770679 | ||||||
chr3:172771020 | A | G | 1 | a0001c0006t0004g0251 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1428+1877A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172771020 | ||||||
chr3:172771054 | G | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0048others(4): Show | 9 | HG01433.hp2 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1428+1911G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172771054 | ||||||
chr3:172771119 | G | A | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1428+1976G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172771119 | ||||||
chr3:172771286 | C | T | 101 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(98): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1428+2143C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172771286 | ||||||
chr3:172771333 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1428+2190G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172771333 | ||||||
chr3:172771607 | A | G | 1 | a0001c0001t0002g0180 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1429-2296A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172771607 | ||||||
chr3:172771622 | T | C | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1429-2281T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172771622 | ||||||
chr3:172771727 | A | G | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.1429-2176A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172771727 | ||||||
chr3:172771786 | G | A | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1429-2117G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172771786 | ||||||
chr3:172771943 | C | T | 10 | a0001c0001t0004g0030a0001c0001t0004g0246a0001c0001t0004g0247others(7): Show | 11 | HG02572.hp2 HG02809.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1429-1960C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172771943 | ||||||
chr3:172772020 | G | A | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1429-1883G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772020 | ||||||
chr3:172772085 | C | T | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1429-1818C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772085 | ||||||
chr3:172772137 | A | C | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1429-1766A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772137 | ||||||
chr3:172772150 | G | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(10): Show | 19 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1429-1753G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772150 | ||||||
chr3:172772153 | A | T | 32 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(29): Show | 38 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(35): Show |
intron_variant | MODIFIER | c.1429-1750A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772153 | ||||||
chr3:172772339 | C | T | 1 | a0001c0001t0003g0220 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1429-1564C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772339 | ||||||
chr3:172772341 | C | T | 6 | a0001c0001t0004g0255a0001c0002t0001g0014a0001c0002t0001g0017others(3): Show | 8 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429-1562C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772341 | ||||||
chr3:172772342 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1429-1561G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772342 | ||||||
chr3:172772349 | C | T | 1 | a0001c0001t0004g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1429-1554C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772349 | ||||||
chr3:172772394 | C | T | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(15): Show | 21 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1429-1509C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772394 | ||||||
chr3:172772431 | C | T | 121 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(118): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1429-1472C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772431 | ||||||
chr3:172772433 | C | T | 2 | a0001c0001t0004g0247a0001c0001t0011g0196 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1429-1470C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772433 | ||||||
chr3:172772438 | C | T | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.1429-1465C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772438 | ||||||
chr3:172772535 | A | G | 1 | a0001c0006t0004g0251 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1429-1368A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772535 | ||||||
chr3:172772551 | G | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(52): Show | 62 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(59): Show |
intron_variant | MODIFIER | c.1429-1352G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772551 | ||||||
chr3:172772704 | G | T | 1 | a0001c0001t0004g0263 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1429-1199G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772704 | ||||||
chr3:172772762 | C | T | 15 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 21 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1429-1141C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172772762 | ||||||
chr3:172773085 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1429-818G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172773085 | ||||||
chr3:172773397 | G | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(52): Show | 62 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(59): Show |
intron_variant | MODIFIER | c.1429-506G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172773397 | ||||||
chr3:172773464 | C | T | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1429-439C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172773464 | ||||||
chr3:172773536 | A | G | 1 | a0001c0001t0009g0060 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1429-367A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172773536 | ||||||
chr3:172773646 | T | C | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1429-257T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172773646 | ||||||
chr3:172773835 | C | T | 1 | a0001c0001t0002g0194 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1429-68C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 13/24 | chr3 | 172773835 | ||||||
chr3:172774118 | G | T | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1548+96G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172774118 | ||||||
chr3:172774136 | T | A | 2 | a0001c0001t0002g0128a0001c0001t0002g0129 | 2 | HG01169.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1548+114T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172774136 | ||||||
chr3:172774146 | G | T | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01255.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1548+124G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172774146 | ||||||
chr3:172774258 | T | C | 122 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(119): Show | 135 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1548+236T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172774258 | ||||||
chr3:172774302 | A | G | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01255.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1548+280A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172774302 | ||||||
chr3:172774405 | C | T | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1548+383C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172774405 | ||||||
chr3:172774498 | CT | C | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1548+485delT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172774498 | |||||
chr3:172774565 | C | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0048a0001c0001t0001g0049others(3): Show | 7 | HG01433.hp2 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1548+543C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172774565 | ||||||
chr3:172774666 | T | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1548+644T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172774666 | ||||||
chr3:172775095 | A | C | 1 | a0001c0001t0004g0244 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1548+1073A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172775095 | ||||||
chr3:172775166 | AGTTTT | A | 105 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(102): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1548+1145_1548+114 others(9): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172775166 | ||||||
chr3:172775238 | A | G | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1548+1216A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172775238 | ||||||
chr3:172775253 | T | C | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1548+1231T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172775253 | ||||||
chr3:172775281 | A | C | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1548+1259A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172775281 | ||||||
chr3:172775361 | T | C | 101 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(98): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1548+1339T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172775361 | ||||||
chr3:172775539 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1548+1517T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172775539 | ||||||
chr3:172775638 | C | CT | 23 | a0001c0001t0002g0200a0001c0001t0003g0239a0001c0001t0004g0030others(20): Show | 24 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(21): Show |
intron_variant | MODIFIER | c.1548+1629dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172775638 | |||||
chr3:172775877 | G | A | 100 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(97): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1548+1855G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172775877 | ||||||
chr3:172776021 | T | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1548+1999T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776021 | ||||||
chr3:172776191 | GTTTTTTC others(2): Show |
G | 31 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(28): Show | 37 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(34): Show |
intron_variant | MODIFIER | c.1548+2176_1548+218 others(13): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172776191 | |||||
chr3:172776198 | C | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 5 | NA18943.hp2 NA18946.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.1548+2176C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776198 | ||||||
chr3:172776198 | C | CT | 6 | a0001c0001t0001g0041a0001c0001t0001g0059a0001c0001t0001g0067others(3): Show | 6 | HG00597.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1548+2199dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172776198 | |||||
chr3:172776198 | C | CTT | 7 | a0001c0001t0001g0105a0001c0001t0001g0212a0001c0002t0001g0014others(4): Show | 9 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1548+2198_1548+219 others(6): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172776198 | |||||
chr3:172776198 | C | T | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1548+2176C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776198 | ||||||
chr3:172776198 | CT | C | 116 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(113): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.1548+2199delT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172776198 | |||||
chr3:172776198 | CTTTTTTT others(2): Show |
C | 21 | a0001c0001t0001g0109a0001c0001t0004g0030a0001c0001t0004g0244others(18): Show | 22 | HG01192.hp1 HG01255.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.1548+2191_1548+219 others(13): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172776198 | |||||
chr3:172776204 | T | C | 2 | a0001c0001t0002g0200a0001c0001t0006g0178 | 2 | HG03927.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1548+2182T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776204 | ||||||
chr3:172776205 | T | C | 97 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(94): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1548+2183T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776205 | ||||||
chr3:172776209 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1548+2187T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776209 | ||||||
chr3:172776210 | T | C | 1 | a0001c0001t0002g0179 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1548+2188T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776210 | ||||||
chr3:172776293 | G | C | 4 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0184others(1): Show | 4 | NA18972.hp1 NA18979.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1548+2271G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776293 | ||||||
chr3:172776357 | C | T | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1548+2335C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776357 | ||||||
chr3:172776358 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1548+2336G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776358 | ||||||
chr3:172776446 | T | G | 105 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(102): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1548+2424T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776446 | ||||||
chr3:172776566 | T | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1548+2544T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776566 | ||||||
chr3:172776578 | A | G | 1 | a0001c0001t0002g0121 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1548+2556A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776578 | ||||||
chr3:172776744 | C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044 | 5 | HG02109.hp2 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1548+2722C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776744 | ||||||
chr3:172776795 | G | A | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1548+2773G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776795 | ||||||
chr3:172776873 | G | GT | 15 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 21 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1548+2864dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172776873 | |||||
chr3:172776905 | C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0082 | 2 | HG01261.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1548+2883C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172776905 | ||||||
chr3:172777210 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1548+3188G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172777210 | ||||||
chr3:172777274 | ATCT | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0048 | 3 | HG01433.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1548+3254_1548+325 others(7): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172777274 | |||||
chr3:172777278 | T | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0048 | 3 | HG01433.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1548+3256T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172777278 | ||||||
chr3:172777652 | A | T | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1548+3630A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172777652 | ||||||
chr3:172777701 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1548+3679C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172777701 | ||||||
chr3:172777731 | G | T | 55 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(52): Show | 62 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(59): Show |
intron_variant | MODIFIER | c.1548+3709G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172777731 | ||||||
chr3:172777734 | A | T | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1548+3712A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172777734 | ||||||
chr3:172777824 | A | G | 1 | a0001c0010t0001g0037 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1548+3802A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172777824 | ||||||
chr3:172777932 | A | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1548+3910A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172777932 | ||||||
chr3:172778086 | C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0004g0245others(1): Show | 4 | HG01167.hp1 HG01361.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1548+4064C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172778086 | ||||||
chr3:172778129 | G | A | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1549-4034G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172778129 | ||||||
chr3:172778481 | C | T | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1549-3682C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172778481 | ||||||
chr3:172778588 | C | CT | 20 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(17): Show | 21 | HG00423.hp1 HG01255.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.1549-3550dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172778588 | |||||
chr3:172778588 | C | CTTT | 6 | a0001c0001t0004g0244a0001c0001t0004g0245a0001c0001t0004g0249others(3): Show | 6 | HG02630.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1549-3552_1549-355 others(7): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172778588 | |||||
chr3:172778588 | CT | C | 113 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(110): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1549-3550delT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172778588 | |||||
chr3:172778588 | CTT | C | 57 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(54): Show | 66 | HG00140.hp1 HG00323.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1549-3551_1549-355 others(6): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172778588 | |||||
chr3:172778588 | CTTT | C | 5 | a0001c0001t0003g0231a0001c0001t0007g0019a0001c0001t0007g0083others(2): Show | 6 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1549-3552_1549-355 others(7): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172778588 | |||||
chr3:172778626 | C | T | 1 | a0001c0001t0002g0182 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1549-3537C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172778626 | ||||||
chr3:172778627 | G | A | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(15): Show | 21 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1549-3536G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172778627 | ||||||
chr3:172778689 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1549-3474G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172778689 | ||||||
chr3:172778706 | C | T | 2 | a0002c0003t0003g0095a0002c0003t0003g0097 | 2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1549-3457C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172778706 | ||||||
chr3:172778742 | C | T | 3 | a0001c0001t0002g0120a0001c0001t0002g0176a0001c0001t0002g0192 | 3 | HG01256.hp1 HG01258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1549-3421C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172778742 | ||||||
chr3:172778744 | C | T | 1 | a0001c0001t0002g0175 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1549-3419C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172778744 | ||||||
chr3:172778745 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1549-3418G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172778745 | ||||||
chr3:172778785 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1549-3378C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172778785 | ||||||
chr3:172778846 | C | T | 217 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(214): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1549-3317C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172778846 | ||||||
chr3:172779426 | A | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1549-2737A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172779426 | ||||||
chr3:172779579 | A | G | 1 | a0006c0008t0001g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1549-2584A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172779579 | ||||||
chr3:172779895 | C | CAAAA | 20 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(17): Show | 21 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.1549-2257_1549-225 others(8): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr3 | 172779895 | |||||
chr3:172779989 | G | C | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1549-2174G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172779989 | ||||||
chr3:172780140 | A | G | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 20 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1549-2023A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172780140 | ||||||
chr3:172780179 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1549-1984A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172780179 | ||||||
chr3:172780272 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1549-1891G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172780272 | ||||||
chr3:172780408 | G | A | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.1549-1755G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172780408 | ||||||
chr3:172780426 | T | C | 105 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(102): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1549-1737T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172780426 | ||||||
chr3:172780476 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1549-1687T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172780476 | ||||||
chr3:172780482 | A | G | 2 | a0001c0001t0004g0107a0001c0001t0004g0108 | 2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1549-1681A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172780482 | ||||||
chr3:172780523 | G | C | 1 | a0001c0001t0001g0053 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1549-1640G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172780523 | ||||||
chr3:172780869 | CTGTT | C | 5 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0045others(2): Show | 7 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1549-1293_1549-129 others(8): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172780869 | ||||||
chr3:172781099 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1549-1064G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172781099 | ||||||
chr3:172781163 | C | G | 1 | a0001c0001t0003g0214 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1549-1000C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172781163 | ||||||
chr3:172781615 | G | T | 1 | a0003c0004t0008g0113 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1549-548G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172781615 | ||||||
chr3:172781634 | A | G | 1 | a0001c0001t0009g0060 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1549-529A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172781634 | ||||||
chr3:172781684 | C | T | 1 | a0001c0001t0003g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1549-479C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172781684 | ||||||
chr3:172782068 | A | T | 20 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(17): Show | 21 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.1549-95A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172782068 | ||||||
chr3:172782084 | T | C | 2 | a0001c0001t0002g0136a0001c0001t0002g0137 | 2 | HG02698.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1549-79T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 14/24 | chr3 | 172782084 | ||||||
chr3:172782247 | CTTTTT | C | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1617+18_1617+22del others(5): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 172782247 | |||||
chr3:172782362 | C | T | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1617+131C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | chr3 | 172782362 | ||||||
chr3:172782420 | G | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(52): Show | 62 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(59): Show |
intron_variant | MODIFIER | c.1617+189G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | chr3 | 172782420 | ||||||
chr3:172782448 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1617+217A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | chr3 | 172782448 | ||||||
chr3:172782809 | T | G | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1617+578T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | chr3 | 172782809 | ||||||
chr3:172782874 | A | AT | 8 | a0001c0001t0002g0120a0001c0001t0002g0173a0001c0001t0002g0176others(5): Show | 8 | HG00280.hp2 HG01109.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1617+653dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr3 | 172782874 | |||||
chr3:172782915 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1617+684G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | chr3 | 172782915 | ||||||
chr3:172782918 | C | G | 3 | a0001c0001t0002g0173a0001c0009t0002g0172a0007c0011t0002g0174 | 3 | HG00280.hp2 HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1617+687C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | chr3 | 172782918 | ||||||
chr3:172783335 | A | T | 2 | a0004c0005t0004g0256a0004c0005t0004g0257 | 2 | HG02717.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1618-464A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | chr3 | 172783335 | ||||||
chr3:172783541 | C | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1618-258C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | chr3 | 172783541 | ||||||
chr3:172783579 | C | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1618-220C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | chr3 | 172783579 | ||||||
chr3:172783622 | A | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1618-177A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | chr3 | 172783622 | ||||||
chr3:172783653 | A | C | 100 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(97): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1618-146A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | chr3 | 172783653 | ||||||
chr3:172783717 | CT | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0048others(4): Show | 9 | HG01433.hp2 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1618-81delT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | chr3 | 172783717 | ||||||
chr3:172783732 | T | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1618-67T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 15/24 | chr3 | 172783732 | ||||||
chr3:172783919 | G | A | 1 | a0003c0004t0008g0111 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1728+10G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 16/24 | chr3 | 172783919 | ||||||
chr3:172784063 | A | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1728+154A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 16/24 | chr3 | 172784063 | ||||||
chr3:172784138 | AT | A | 7 | a0001c0001t0001g0068a0001c0001t0002g0138a0001c0001t0002g0139others(4): Show | 7 | HG01975.hp1 HG02155.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1728+243delT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr3 | 172784138 | |||||
chr3:172784163 | C | T | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(15): Show | 21 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1728+254C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 16/24 | chr3 | 172784163 | ||||||
chr3:172784198 | C | T | 6 | a0001c0001t0001g0016a0001c0001t0001g0048a0001c0001t0001g0049others(3): Show | 7 | HG01433.hp2 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1728+289C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 16/24 | chr3 | 172784198 | ||||||
chr3:172784234 | C | T | 5 | a0001c0001t0001g0074a0001c0001t0007g0019a0001c0001t0007g0083others(2): Show | 6 | HG01192.hp2 HG02735.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.1728+325C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 16/24 | chr3 | 172784234 | ||||||
chr3:172784259 | C | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1728+350C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 16/24 | chr3 | 172784259 | ||||||
chr3:172784327 | A | T | 1 | a0001c0001t0004g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1729-380A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 16/24 | chr3 | 172784327 | ||||||
chr3:172784347 | C | G | 168 | a0001c0001t0001g0074a0001c0001t0001g0093a0001c0001t0002g0001others(165): Show | 188 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1729-360C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 16/24 | chr3 | 172784347 | ||||||
chr3:172784368 | T | C | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1729-339T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 16/24 | chr3 | 172784368 | ||||||
chr3:172784530 | G | A | 1 | a0001c0001t0003g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1729-177G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 16/24 | chr3 | 172784530 | ||||||
chr3:172784648 | T | C | 32 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(29): Show | 38 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(35): Show |
intron_variant | MODIFIER | c.1729-59T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 16/24 | chr3 | 172784648 | ||||||
chr3:172784831 | A | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1825+28A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172784831 | ||||||
chr3:172785038 | T | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1825+235T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172785038 | ||||||
chr3:172785122 | G | A | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.1825+319G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172785122 | ||||||
chr3:172785221 | G | C | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1825+418G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172785221 | ||||||
chr3:172785251 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1825+448A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172785251 | ||||||
chr3:172785327 | G | T | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1825+524G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172785327 | ||||||
chr3:172785434 | C | T | 100 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(97): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1825+631C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172785434 | ||||||
chr3:172785517 | T | TA | 5 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0002g0140others(2): Show | 7 | HG02109.hp2 HG03139.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825+727dupA | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr3 | 172785517 | |||||
chr3:172785751 | C | T | 4 | a0001c0001t0002g0195a0001c0001t0006g0123a0001c0001t0006g0124others(1): Show | 4 | HG00741.hp2 HG01517.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-742C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172785751 | ||||||
chr3:172785829 | T | C | 55 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(52): Show | 62 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(59): Show |
intron_variant | MODIFIER | c.1826-664T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172785829 | ||||||
chr3:172785988 | C | A | 5 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0045others(2): Show | 7 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-505C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172785988 | ||||||
chr3:172786014 | A | T | 1 | a0001c0001t0001g0008 | 3 | NA18941.hp2 NA18944.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1826-479A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172786014 | ||||||
chr3:172786055 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1826-438C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172786055 | ||||||
chr3:172786181 | T | A | 1 | a0001c0001t0005g0198 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1826-312T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172786181 | ||||||
chr3:172786236 | A | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1826-257A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172786236 | ||||||
chr3:172786268 | A | G | 1 | a0001c0001t0003g0230 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1826-225A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172786268 | ||||||
chr3:172786462 | T | A | 1 | a0001c0001t0001g0031 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1826-31T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 17/24 | chr3 | 172786462 | ||||||
chr3:172786780 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1907+206A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172786780 | ||||||
chr3:172786852 | A | G | 5 | a0001c0001t0002g0135a0001c0001t0002g0169a0001c0001t0002g0170others(2): Show | 5 | HG00423.hp2 NA18951.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1907+278A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172786852 | ||||||
chr3:172786890 | T | G | 1 | a0001c0001t0002g0141 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1907+316T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172786890 | ||||||
chr3:172786934 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1907+360A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172786934 | ||||||
chr3:172787011 | C | T | 4 | a0001c0001t0002g0168a0001c0001t0002g0191a0001c0001t0002g0201others(1): Show | 4 | HG00140.hp2 HG01891.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907+437C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172787011 | ||||||
chr3:172787097 | G | A | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1907+523G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172787097 | ||||||
chr3:172787199 | A | G | 1 | a0001c0001t0002g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1907+625A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172787199 | ||||||
chr3:172787325 | G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 4 | NA18947.hp2 NA18965.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907+751G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172787325 | ||||||
chr3:172787368 | C | CTTAT | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1907+796_1907+797i others(6): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172787368 | |||||
chr3:172787595 | C | A | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(255): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1907+1021C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172787595 | ||||||
chr3:172787658 | T | G | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.1907+1084T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172787658 | ||||||
chr3:172787750 | C | T | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1907+1176C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172787750 | ||||||
chr3:172787767 | A | G | 1 | a0004c0005t0004g0257 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1907+1193A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172787767 | ||||||
chr3:172787791 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1907+1217A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172787791 | ||||||
chr3:172788173 | T | C | 100 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(97): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1907+1599T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172788173 | ||||||
chr3:172788226 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1907+1652A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172788226 | ||||||
chr3:172788425 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1907+1851A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172788425 | ||||||
chr3:172788460 | G | A | 100 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(97): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1907+1886G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172788460 | ||||||
chr3:172788473 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1907+1899G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172788473 | ||||||
chr3:172788640 | A | T | 7 | a0001c0001t0002g0027a0001c0001t0002g0165a0001c0001t0002g0166others(4): Show | 8 | HG01433.hp1 NA18947.hp1 NA18981.hp2 others(5): Show |
intron_variant | MODIFIER | c.1907+2066A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172788640 | ||||||
chr3:172788662 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1907+2088G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172788662 | ||||||
chr3:172788774 | A | C | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1907+2200A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172788774 | ||||||
chr3:172788833 | G | T | 3 | a0001c0001t0002g0140a0001c0001t0002g0181a0001c0001t0002g0197 | 3 | NA18964.hp2 NA18977.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1907+2259G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172788833 | ||||||
chr3:172788842 | G | A | 1 | a0001c0001t0004g0252 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1907+2268G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172788842 | ||||||
chr3:172788912 | G | C | 4 | a0001c0001t0002g0186a0001c0001t0002g0203a0001c0001t0002g0205others(1): Show | 4 | HG01175.hp1 HG01496.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907+2338G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172788912 | ||||||
chr3:172788973 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1907+2399G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172788973 | ||||||
chr3:172789057 | C | CA | 117 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(114): Show | 136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1907+2501dupA | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172789057 | |||||
chr3:172789057 | C | CAA | 8 | a0001c0001t0001g0088a0001c0001t0001g0093a0001c0001t0002g0136others(5): Show | 9 | HG00735.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1907+2500_1907+250 others(6): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172789057 | |||||
chr3:172789095 | T | C | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1907+2521T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172789095 | ||||||
chr3:172789125 | G | A | 2 | a0001c0001t0004g0107a0001c0001t0004g0108 | 2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1907+2551G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172789125 | ||||||
chr3:172789163 | C | G | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1907+2589C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172789163 | ||||||
chr3:172789220 | G | GT | 6 | a0001c0001t0001g0079a0001c0001t0003g0216a0001c0001t0003g0229others(3): Show | 6 | HG03579.hp1 HG03942.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.1907+2662dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172789220 | |||||
chr3:172789220 | GT | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(179): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1907+2662delT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172789220 | |||||
chr3:172789247 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1907+2673C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172789247 | ||||||
chr3:172789249 | C | T | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1907+2675C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172789249 | ||||||
chr3:172789364 | T | G | 1 | a0001c0001t0002g0144 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1907+2790T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172789364 | ||||||
chr3:172789409 | G | T | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(15): Show | 21 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1907+2835G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172789409 | ||||||
chr3:172789501 | G | C | 1 | a0001c0006t0004g0251 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1907+2927G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172789501 | ||||||
chr3:172789669 | T | G | 1 | a0001c0001t0002g0187 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1907+3095T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172789669 | ||||||
chr3:172789672 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1907+3098G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172789672 | ||||||
chr3:172789998 | AT | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 21 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1907+3435delT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172789998 | |||||
chr3:172790134 | C | T | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1907+3560C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172790134 | ||||||
chr3:172790190 | A | T | 1 | a0001c0001t0002g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1907+3616A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172790190 | ||||||
chr3:172790466 | A | G | 3 | a0001c0001t0003g0214a0001c0001t0003g0217a0001c0001t0003g0228 | 3 | NA18968.hp1 NA18988.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1907+3892A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172790466 | ||||||
chr3:172790496 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1907+3922A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172790496 | ||||||
chr3:172790566 | C | G | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1907+3992C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172790566 | ||||||
chr3:172790586 | T | G | 5 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0001g0102others(2): Show | 6 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.1907+4012T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172790586 | ||||||
chr3:172790699 | A | T | 1 | a0001c0001t0004g0261 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1907+4125A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172790699 | ||||||
chr3:172790757 | T | C | 1 | a0001c0001t0007g0098 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1907+4183T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172790757 | ||||||
chr3:172791019 | A | T | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1907+4445A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172791019 | ||||||
chr3:172791365 | G | T | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1907+4791G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172791365 | ||||||
chr3:172791402 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1907+4828C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172791402 | ||||||
chr3:172791462 | A | G | 2 | a0001c0001t0002g0143a0001c0001t0002g0164 | 2 | HG00735.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1907+4888A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172791462 | ||||||
chr3:172791465 | T | A | 2 | a0001c0001t0002g0143a0001c0001t0002g0164 | 2 | HG00735.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1907+4891T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172791465 | ||||||
chr3:172791466 | T | C | 2 | a0001c0001t0002g0143a0001c0001t0002g0164 | 2 | HG00735.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1907+4892T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172791466 | ||||||
chr3:172791475 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1907+4901A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172791475 | ||||||
chr3:172791713 | C | G | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1907+5139C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172791713 | ||||||
chr3:172791811 | A | C | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1907+5237A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172791811 | ||||||
chr3:172791813 | C | T | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.1907+5239C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172791813 | ||||||
chr3:172791825 | A | G | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 20 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1907+5251A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172791825 | ||||||
chr3:172791841 | C | T | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1907+5267C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172791841 | ||||||
chr3:172792253 | G | T | 1 | a0001c0001t0002g0180 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1907+5679G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172792253 | ||||||
chr3:172792432 | C | T | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01255.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1907+5858C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172792432 | ||||||
chr3:172792438 | G | A | 165 | a0001c0001t0001g0093a0001c0001t0002g0001a0001c0001t0002g0004others(162): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1907+5864G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172792438 | ||||||
chr3:172792451 | C | CT | 38 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0031others(35): Show | 41 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1907+5891dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172792451 | |||||
chr3:172792451 | C | CTT | 100 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(97): Show | 112 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.1907+5890_1907+589 others(6): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172792451 | |||||
chr3:172792451 | CT | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0018others(28): Show | 40 | HG00438.hp2 HG01192.hp2 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.1907+5891delT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172792451 | |||||
chr3:172792471 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1907+5897C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172792471 | ||||||
chr3:172792612 | T | G | 2 | a0001c0001t0002g0118a0001c0001t0002g0119 | 2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1907+6038T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172792612 | ||||||
chr3:172792934 | G | A | 2 | a0002c0003t0003g0095a0002c0003t0003g0097 | 2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1907+6360G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172792934 | ||||||
chr3:172792971 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1907+6397C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172792971 | ||||||
chr3:172793089 | C | T | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 20 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1907+6515C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172793089 | ||||||
chr3:172793300 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1907+6726G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172793300 | ||||||
chr3:172793353 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1907+6779C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172793353 | ||||||
chr3:172793374 | A | C | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1907+6800A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172793374 | ||||||
chr3:172793421 | G | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0001g0102others(4): Show | 8 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1907+6847G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172793421 | ||||||
chr3:172793442 | C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044 | 5 | HG02109.hp2 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1907+6868C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172793442 | ||||||
chr3:172793482 | A | G | 1 | a0001c0001t0002g0264 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1907+6908A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172793482 | ||||||
chr3:172793519 | A | G | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1907+6945A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172793519 | ||||||
chr3:172793524 | C | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0025others(11): Show | 22 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1907+6950C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172793524 | ||||||
chr3:172793618 | C | T | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.1907+7044C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172793618 | ||||||
chr3:172793756 | A | C | 5 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0045others(2): Show | 7 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1907+7182A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172793756 | ||||||
chr3:172794005 | A | T | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1907+7431A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172794005 | ||||||
chr3:172794283 | G | A | 1 | a0003c0004t0008g0114 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1907+7709G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172794283 | ||||||
chr3:172794449 | T | C | 1 | a0001c0001t0013g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1907+7875T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172794449 | ||||||
chr3:172794451 | GA | G | 32 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(29): Show | 38 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(35): Show |
intron_variant | MODIFIER | c.1907+7878delA | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172794451 | ||||||
chr3:172794493 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1907+7919T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172794493 | ||||||
chr3:172794622 | A | AAAC | 25 | a0001c0001t0001g0106a0001c0001t0002g0125a0001c0001t0002g0126others(22): Show | 25 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1908-7973_1908-797 others(7): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172794622 | |||||
chr3:172794662 | T | A | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0048others(4): Show | 9 | HG01433.hp2 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1908-7954T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172794662 | ||||||
chr3:172794740 | G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0044a0001c0001t0004g0260 | 5 | HG02109.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1908-7876G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172794740 | ||||||
chr3:172794784 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1908-7832G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172794784 | ||||||
chr3:172794801 | G | A | 2 | a0001c0001t0004g0245a0001c0006t0004g0251 | 2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1908-7815G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172794801 | ||||||
chr3:172794829 | G | A | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1908-7787G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172794829 | ||||||
chr3:172794880 | A | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0110 | 3 | HG02602.hp2 HG02738.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1908-7736A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172794880 | ||||||
chr3:172795011 | C | T | 1 | a0008c0012t0003g0221 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1908-7605C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172795011 | ||||||
chr3:172795137 | G | A | 1 | a0001c0001t0004g0244 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1908-7479G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172795137 | ||||||
chr3:172795211 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1908-7405C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172795211 | ||||||
chr3:172795292 | C | A | 105 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(102): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1908-7324C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172795292 | ||||||
chr3:172795294 | C | G | 105 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(102): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1908-7322C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172795294 | ||||||
chr3:172795295 | C | G | 105 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(102): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1908-7321C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172795295 | ||||||
chr3:172795308 | A | C | 1 | a0001c0001t0002g0161 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1908-7308A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172795308 | ||||||
chr3:172795323 | C | CA | 10 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0062others(7): Show | 10 | HG01074.hp1 HG01358.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1908-7272dupA | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172795323 | |||||
chr3:172795323 | CA | C | 62 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(59): Show | 72 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.1908-7272delA | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172795323 | |||||
chr3:172795323 | CAA | C | 46 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(43): Show | 58 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1908-7273_1908-727 others(6): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172795323 | |||||
chr3:172795325 | A | C | 5 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0045others(2): Show | 7 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1908-7291A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172795325 | ||||||
chr3:172795344 | A | T | 1 | a0006c0008t0001g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1908-7272A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172795344 | ||||||
chr3:172795620 | T | C | 1 | a0006c0008t0001g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1908-6996T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172795620 | ||||||
chr3:172795651 | A | G | 1 | a0001c0001t0003g0265 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1908-6965A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172795651 | ||||||
chr3:172795821 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1908-6795A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172795821 | ||||||
chr3:172795894 | A | G | 2 | a0001c0001t0006g0123a0001c0001t0006g0124 | 2 | HG00741.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1908-6722A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172795894 | ||||||
chr3:172795970 | C | T | 1 | a0003c0004t0008g0114 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1908-6646C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172795970 | ||||||
chr3:172796263 | A | G | 100 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(97): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1908-6353A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172796263 | ||||||
chr3:172796280 | G | A | 16 | a0001c0001t0004g0030a0001c0001t0004g0245a0001c0001t0004g0246others(13): Show | 17 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1908-6336G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172796280 | ||||||
chr3:172796369 | A | G | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1908-6247A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172796369 | ||||||
chr3:172796396 | A | G | 1 | a0001c0001t0001g0010 | 3 | HG02109.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1908-6220A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172796396 | ||||||
chr3:172796400 | A | G | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1908-6216A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172796400 | ||||||
chr3:172796504 | G | A | 199 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(196): Show | 232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1908-6112G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172796504 | ||||||
chr3:172796608 | T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0087 | 3 | HG02717.hp1 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1908-6008T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172796608 | ||||||
chr3:172796711 | G | A | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1908-5905G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172796711 | ||||||
chr3:172796759 | C | T | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1908-5857C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172796759 | ||||||
chr3:172796797 | G | A | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01255.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1908-5819G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172796797 | ||||||
chr3:172796922 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1908-5694G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172796922 | ||||||
chr3:172796951 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1908-5665G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172796951 | ||||||
chr3:172796968 | A | T | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1908-5648A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172796968 | ||||||
chr3:172797018 | C | CAGATTCA others(17): Show |
3 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084 | 4 | HG01192.hp2 HG03710.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1908-5598_1908-559 others(28): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172797018 | ||||||
chr3:172797018 | C | CAGATTCA others(21): Show |
1 | a0001c0001t0007g0098 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1908-5598_1908-559 others(32): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172797018 | ||||||
chr3:172797018 | C | CTG | 21 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0023others(18): Show | 28 | HG00280.hp1 HG00323.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.1908-5564_1908-556 others(6): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172797018 | |||||
chr3:172797018 | C | CTGTG | 21 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(18): Show | 27 | HG00673.hp1 HG00741.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1908-5566_1908-556 others(8): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172797018 | |||||
chr3:172797018 | C | CTGTGTG | 8 | a0001c0001t0002g0119a0001c0001t0002g0126a0001c0001t0002g0147others(5): Show | 8 | HG00597.hp1 HG02040.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.1908-5568_1908-556 others(10): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172797018 | |||||
chr3:172797018 | C | CTGTGTGT others(1): Show |
31 | a0001c0001t0002g0026a0001c0001t0002g0131a0001c0001t0002g0144others(28): Show | 34 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.1908-5570_1908-556 others(12): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172797018 | |||||
chr3:172797018 | C | CTGTGTGT others(3): Show |
55 | a0001c0001t0002g0001a0001c0001t0002g0027a0001c0001t0002g0118others(52): Show | 64 | HG00621.hp1 HG00642.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.1908-5572_1908-556 others(14): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172797018 | |||||
chr3:172797018 | C | CTGTGTGT others(5): Show |
36 | a0001c0001t0002g0004a0001c0001t0002g0121a0001c0001t0002g0129others(33): Show | 39 | HG00423.hp2 HG00558.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1908-5574_1908-556 others(16): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172797018 | |||||
chr3:172797018 | C | CTGTGTGT others(7): Show |
16 | a0001c0001t0001g0093a0001c0001t0002g0028a0001c0001t0002g0134others(13): Show | 17 | HG00280.hp2 HG00408.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.1908-5576_1908-556 others(18): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172797018 | |||||
chr3:172797018 | C | CTGTGTGT others(9): Show |
7 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0175others(4): Show | 7 | HG02698.hp1 HG02965.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1908-5578_1908-556 others(20): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172797018 | |||||
chr3:172797018 | C | CTGTGTGT others(11): Show |
1 | a0007c0011t0002g0174 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1908-5580_1908-556 others(22): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172797018 | |||||
chr3:172797018 | C | CTGTGTGT others(15): Show |
1 | a0001c0001t0004g0244 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1908-5584_1908-556 others(26): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172797018 | |||||
chr3:172797018 | C | CTGTGTGT others(23): Show |
1 | a0001c0001t0004g0249 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1908-5592_1908-556 others(34): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172797018 | |||||
chr3:172797018 | CTG | C | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0087others(2): Show | 7 | HG01884.hp2 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1908-5564_1908-556 others(6): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172797018 | |||||
chr3:172797018 | CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1908-5574_1908-556 others(16): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172797018 | |||||
chr3:172797183 | C | G | 1 | a0001c0001t0002g0153 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1908-5433C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172797183 | ||||||
chr3:172797204 | A | AT | 103 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0051others(100): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1908-5399dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172797204 | |||||
chr3:172797218 | A | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1908-5398A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172797218 | ||||||
chr3:172797263 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1908-5353G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172797263 | ||||||
chr3:172797406 | C | T | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.1908-5210C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172797406 | ||||||
chr3:172797460 | C | G | 1 | a0001c0001t0001g0025 | 2 | NA18977.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1908-5156C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172797460 | ||||||
chr3:172797553 | T | C | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1908-5063T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172797553 | ||||||
chr3:172797629 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1908-4987A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172797629 | ||||||
chr3:172797973 | T | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0183 | 3 | NA18947.hp1 NA18983.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1908-4643T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172797973 | ||||||
chr3:172798403 | T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0044 | 5 | HG02109.hp2 HG02965.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1908-4213T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172798403 | ||||||
chr3:172798408 | A | G | 5 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0045others(2): Show | 7 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1908-4208A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172798408 | ||||||
chr3:172798544 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1908-4072A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172798544 | ||||||
chr3:172798643 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1908-3973T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172798643 | ||||||
chr3:172798644 | C | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1908-3972C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172798644 | ||||||
chr3:172798681 | T | C | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.1908-3935T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172798681 | ||||||
chr3:172798794 | T | C | 2 | a0001c0001t0002g0147a0001c0001t0002g0179 | 2 | HG00597.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1908-3822T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172798794 | ||||||
chr3:172798993 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1908-3623C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172798993 | ||||||
chr3:172798996 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1908-3620C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172798996 | ||||||
chr3:172799255 | C | G | 1 | a0001c0001t0002g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1908-3361C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172799255 | ||||||
chr3:172799323 | C | G | 2 | a0001c0001t0004g0107a0001c0001t0004g0108 | 2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1908-3293C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172799323 | ||||||
chr3:172799654 | A | G | 14 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0025others(11): Show | 22 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1908-2962A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172799654 | ||||||
chr3:172799681 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1908-2935A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172799681 | ||||||
chr3:172799745 | C | G | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1908-2871C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172799745 | ||||||
chr3:172800082 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1908-2534G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172800082 | ||||||
chr3:172800296 | T | C | 60 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(57): Show | 68 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(65): Show |
intron_variant | MODIFIER | c.1908-2320T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172800296 | ||||||
chr3:172800400 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1908-2216G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172800400 | ||||||
chr3:172800579 | T | A | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1908-2037T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172800579 | ||||||
chr3:172800662 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1908-1954C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172800662 | ||||||
chr3:172800942 | T | C | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.1908-1674T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172800942 | ||||||
chr3:172800958 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1908-1658A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172800958 | ||||||
chr3:172801078 | A | G | 39 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(36): Show | 46 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(43): Show |
intron_variant | MODIFIER | c.1908-1538A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172801078 | ||||||
chr3:172801116 | A | C | 1 | a0001c0001t0001g0010 | 3 | HG02109.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1908-1500A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172801116 | ||||||
chr3:172801131 | A | T | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1908-1485A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172801131 | ||||||
chr3:172801284 | T | C | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1908-1332T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172801284 | ||||||
chr3:172801551 | A | G | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1908-1065A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172801551 | ||||||
chr3:172801614 | C | T | 1 | a0001c0001t0012g0130 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1908-1002C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172801614 | ||||||
chr3:172801805 | G | A | 161 | a0001c0001t0001g0093a0001c0001t0002g0001a0001c0001t0002g0004others(158): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1908-811G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172801805 | ||||||
chr3:172802094 | G | GTTTTGT | 3 | a0001c0001t0003g0216a0001c0001t0003g0236a0001c0001t0003g0265 | 3 | HG02622.hp1 NA18957.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1908-493_1908-488d others(8): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172802094 | |||||
chr3:172802094 | G | GTTTTGTT others(5): Show |
30 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(27): Show | 36 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(33): Show |
intron_variant | MODIFIER | c.1908-499_1908-488d others(14): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172802094 | |||||
chr3:172802094 | G | GTTTTGTT others(11): Show |
1 | a0001c0001t0003g0227 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1908-505_1908-488d others(20): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172802094 | |||||
chr3:172802094 | GTTTTGT | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(5): Show | 12 | HG01433.hp2 HG01891.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1908-493_1908-488d others(8): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172802094 | |||||
chr3:172802094 | GTTTTGTT others(5): Show |
G | 3 | a0001c0001t0007g0019a0001c0001t0007g0084a0001c0001t0007g0098 | 4 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1908-499_1908-488d others(14): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172802094 | |||||
chr3:172802112 | TTTTTGTT others(4): Show |
T | 1 | a0001c0001t0007g0083 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1908-499_1908-489d others(13): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr3 | 172802112 | |||||
chr3:172802331 | C | T | 1 | a0006c0008t0001g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1908-285C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172802331 | ||||||
chr3:172802359 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1908-257C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172802359 | ||||||
chr3:172802362 | C | G | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.1908-254C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172802362 | ||||||
chr3:172802382 | G | A | 1 | a0001c0001t0004g0252 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1908-234G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172802382 | ||||||
chr3:172802383 | G | T | 2 | a0001c0001t0002g0026a0001c0001t0013g0122 | 3 | HG02071.hp1 NA18969.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1908-233G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172802383 | ||||||
chr3:172802392 | C | T | 1 | a0001c0001t0003g0216 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1908-224C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 18/24 | chr3 | 172802392 | ||||||
chr3:172802773 | T | C | 1 | a0001c0001t0003g0224 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1986+79T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 19/24 | chr3 | 172802773 | ||||||
chr3:172803028 | G | C | 217 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(214): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2106+48G>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172803028 | ||||||
chr3:172803158 | G | A | 161 | a0001c0001t0001g0093a0001c0001t0002g0001a0001c0001t0002g0004others(158): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2106+178G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172803158 | ||||||
chr3:172803252 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2106+272T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172803252 | ||||||
chr3:172803519 | C | A | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2106+539C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172803519 | ||||||
chr3:172803667 | A | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 20 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.2106+687A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172803667 | ||||||
chr3:172803674 | A | T | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2106+694A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172803674 | ||||||
chr3:172803812 | C | CT | 14 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(11): Show | 20 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.2106+842dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr3 | 172803812 | |||||
chr3:172803927 | C | T | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2106+947C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172803927 | ||||||
chr3:172804555 | A | G | 20 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(17): Show | 21 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.2107-1176A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172804555 | ||||||
chr3:172804742 | T | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.2107-989T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172804742 | ||||||
chr3:172804891 | AT | A | 161 | a0001c0001t0001g0077a0001c0001t0001g0093a0001c0001t0002g0001others(158): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2107-830delT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr3 | 172804891 | |||||
chr3:172805151 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2107-580G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172805151 | ||||||
chr3:172805204 | TATACTGA others(3): Show |
T | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.2107-526_2107-517d others(12): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172805204 | ||||||
chr3:172805255 | T | A | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107-476T>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172805255 | ||||||
chr3:172805279 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2107-452T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172805279 | ||||||
chr3:172805279 | T | TA | 5 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0001g0102others(2): Show | 6 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.2107-449dupA | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr3 | 172805279 | |||||
chr3:172805420 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2107-311C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172805420 | ||||||
chr3:172805450 | C | T | 1 | a0001c0002t0001g0017 | 2 | HG02109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2107-281C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172805450 | ||||||
chr3:172805515 | C | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0048others(4): Show | 9 | HG01433.hp2 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2107-216C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172805515 | ||||||
chr3:172805564 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2107-167A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172805564 | ||||||
chr3:172805595 | T | G | 1 | a0001c0001t0002g0194 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2107-136T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172805595 | ||||||
chr3:172805649 | G | A | 1 | a0001c0001t0013g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2107-82G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 20/24 | chr3 | 172805649 | ||||||
chr3:172806581 | T | C | 1 | a0001c0001t0002g0154 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2245+712T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 21/24 | chr3 | 172806581 | ||||||
chr3:172806597 | C | CT | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0048others(5): Show | 10 | HG01433.hp2 HG01891.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.2245+744dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr3 | 172806597 | |||||
chr3:172806597 | CT | C | 10 | a0001c0001t0002g0143a0001c0001t0002g0164a0001c0001t0004g0260others(7): Show | 13 | HG00735.hp1 HG01123.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.2245+744delT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr3 | 172806597 | |||||
chr3:172806597 | CTT | C | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.2245+743_2245+744d others(4): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr3 | 172806597 | |||||
chr3:172806651 | G | GT | 16 | a0001c0001t0001g0002a0001c0001t0001g0025a0001c0001t0001g0053others(13): Show | 22 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.2245+801dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr3 | 172806651 | |||||
chr3:172806651 | GT | G | 58 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0002g0158others(55): Show | 66 | HG00621.hp2 HG00673.hp1 HG01167.hp1 others(63): Show |
intron_variant | MODIFIER | c.2245+801delT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr3 | 172806651 | |||||
chr3:172806651 | GTT | G | 140 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(137): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.2245+800_2245+801d others(4): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr3 | 172806651 | |||||
chr3:172806651 | GTTT | G | 14 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(11): Show | 20 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.2245+799_2245+801d others(5): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr3 | 172806651 | |||||
chr3:172806655 | T | G | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2245+786T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 21/24 | chr3 | 172806655 | ||||||
chr3:172806785 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2245+916C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 21/24 | chr3 | 172806785 | ||||||
chr3:172806857 | G | A | 1 | a0001c0010t0001g0037 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2246-913G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 21/24 | chr3 | 172806857 | ||||||
chr3:172806862 | T | C | 60 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(57): Show | 68 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(65): Show |
intron_variant | MODIFIER | c.2246-908T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 21/24 | chr3 | 172806862 | ||||||
chr3:172806972 | A | C | 102 | a0001c0001t0001g0077a0001c0001t0002g0001a0001c0001t0002g0004others(99): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2246-798A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 21/24 | chr3 | 172806972 | ||||||
chr3:172807323 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2246-447C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 21/24 | chr3 | 172807323 | ||||||
chr3:172808228 | C | A | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400+304C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172808228 | ||||||
chr3:172808375 | C | CA | 25 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(22): Show | 28 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.2400+466dupA | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 172808375 | |||||
chr3:172808585 | C | A | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.2400+661C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172808585 | ||||||
chr3:172809298 | G | A | 161 | a0001c0001t0001g0093a0001c0001t0002g0001a0001c0001t0002g0004others(158): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2400+1374G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172809298 | ||||||
chr3:172809411 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2400+1487T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172809411 | ||||||
chr3:172809501 | T | G | 1 | a0001c0001t0004g0255 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2400+1577T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172809501 | ||||||
chr3:172809568 | T | TAC | 9 | a0001c0001t0001g0056a0001c0001t0001g0079a0001c0001t0002g0027others(6): Show | 10 | HG02717.hp2 HG02723.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.2400+1673_2400+167 others(6): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 172809568 | |||||
chr3:172809568 | TAC | T | 160 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(157): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.2400+1673_2400+167 others(6): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 172809568 | |||||
chr3:172809568 | TACAC | T | 44 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0031others(41): Show | 50 | HG00323.hp2 HG00642.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.2400+1671_2400+167 others(8): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 172809568 | |||||
chr3:172809568 | TACACAC | T | 10 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(7): Show | 13 | HG00099.hp2 HG00140.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.2400+1669_2400+167 others(10): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 172809568 | |||||
chr3:172809587 | ACACACAC others(5): Show |
A | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2400+1676_2400+168 others(16): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 172809587 | |||||
chr3:172809595 | A | G | 1 | a0001c0001t0003g0235 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2400+1671A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172809595 | ||||||
chr3:172809598 | C | T | 1 | a0008c0012t0003g0221 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2400+1674C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172809598 | ||||||
chr3:172809611 | G | A | 55 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(52): Show | 62 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(59): Show |
intron_variant | MODIFIER | c.2400+1687G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172809611 | ||||||
chr3:172810030 | G | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 20 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.2400+2106G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172810030 | ||||||
chr3:172810187 | A | C | 200 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(197): Show | 233 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2400+2263A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172810187 | ||||||
chr3:172810193 | C | T | 1 | a0001c0001t0002g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2400+2269C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172810193 | ||||||
chr3:172810244 | A | G | 100 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(97): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.2400+2320A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172810244 | ||||||
chr3:172810262 | C | T | 100 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(97): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.2400+2338C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172810262 | ||||||
chr3:172810523 | C | T | 5 | a0001c0001t0001g0041a0001c0001t0007g0019a0001c0001t0007g0083others(2): Show | 6 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.2400+2599C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172810523 | ||||||
chr3:172810647 | G | A | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.2400+2723G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172810647 | ||||||
chr3:172810730 | G | A | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2400+2806G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172810730 | ||||||
chr3:172810877 | T | G | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2400+2953T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172810877 | ||||||
chr3:172811213 | G | GT | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2400+3294dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 172811213 | |||||
chr3:172811484 | T | C | 5 | a0002c0003t0003g0022a0002c0003t0003g0094a0002c0003t0003g0095others(2): Show | 6 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2400+3560T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172811484 | ||||||
chr3:172811575 | A | T | 1 | a0001c0001t0002g0144 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2400+3651A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172811575 | ||||||
chr3:172811590 | T | G | 1 | a0001c0001t0002g0134 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2400+3666T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172811590 | ||||||
chr3:172811667 | G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042 | 3 | NA18965.hp1 NA19081.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2400+3743G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172811667 | ||||||
chr3:172811900 | A | G | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2401-3704A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172811900 | ||||||
chr3:172811910 | T | C | 3 | a0001c0001t0004g0107a0001c0001t0004g0108a0001c0001t0011g0196 | 3 | HG02976.hp2 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2401-3694T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172811910 | ||||||
chr3:172811983 | C | CT | 29 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(26): Show | 35 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.2401-3605dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 172811983 | |||||
chr3:172812061 | T | C | 265 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(262): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2401-3543T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172812061 | ||||||
chr3:172812071 | A | G | 17 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 20 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.2401-3533A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172812071 | ||||||
chr3:172812094 | G | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.2401-3510G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172812094 | ||||||
chr3:172812144 | C | T | 4 | a0001c0001t0006g0123a0001c0001t0006g0124a0001c0001t0006g0142others(1): Show | 4 | HG00741.hp2 HG01517.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.2401-3460C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172812144 | ||||||
chr3:172812198 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2401-3406C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172812198 | ||||||
chr3:172812258 | G | T | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2401-3346G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172812258 | ||||||
chr3:172812285 | T | C | 265 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(262): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2401-3319T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172812285 | ||||||
chr3:172812669 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2401-2935C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172812669 | ||||||
chr3:172812972 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2401-2632G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172812972 | ||||||
chr3:172813006 | A | AT | 4 | a0003c0004t0008g0111a0003c0004t0008g0112a0003c0004t0008g0113others(1): Show | 4 | HG01884.hp1 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2401-2597dupT | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 172813006 | |||||
chr3:172813087 | T | C | 1 | a0006c0008t0001g0076 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2401-2517T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172813087 | ||||||
chr3:172813093 | A | G | 57 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(54): Show | 64 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(61): Show |
intron_variant | MODIFIER | c.2401-2511A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172813093 | ||||||
chr3:172813130 | A | G | 1 | a0001c0001t0003g0239 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2401-2474A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172813130 | ||||||
chr3:172813211 | G | A | 1 | a0001c0001t0002g0264 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2401-2393G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172813211 | ||||||
chr3:172813423 | A | G | 34 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(31): Show | 40 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(37): Show |
intron_variant | MODIFIER | c.2401-2181A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172813423 | ||||||
chr3:172813542 | C | T | 3 | a0001c0001t0002g0173a0001c0009t0002g0172a0007c0011t0002g0174 | 3 | HG00280.hp2 HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.2401-2062C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172813542 | ||||||
chr3:172813700 | C | T | 100 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(97): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.2401-1904C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172813700 | ||||||
chr3:172813870 | A | G | 163 | a0001c0001t0001g0093a0001c0001t0002g0001a0001c0001t0002g0004others(160): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.2401-1734A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172813870 | ||||||
chr3:172813906 | G | GA | 163 | a0001c0001t0001g0093a0001c0001t0002g0001a0001c0001t0002g0004others(160): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.2401-1696dupA | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr3 | 172813906 | |||||
chr3:172814079 | G | A | 57 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(54): Show | 64 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(61): Show |
intron_variant | MODIFIER | c.2401-1525G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172814079 | ||||||
chr3:172814133 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2401-1471A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172814133 | ||||||
chr3:172814284 | T | G | 1 | a0001c0001t0003g0239 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2401-1320T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172814284 | ||||||
chr3:172814473 | G | T | 1 | a0001c0001t0003g0226 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2401-1131G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172814473 | ||||||
chr3:172814809 | C | A | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.2401-795C>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172814809 | ||||||
chr3:172814817 | A | G | 262 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(259): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2401-787A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172814817 | ||||||
chr3:172815000 | C | T | 161 | a0001c0001t0001g0093a0001c0001t0002g0001a0001c0001t0002g0004others(158): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2401-604C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172815000 | ||||||
chr3:172815011 | A | G | 1 | a0001c0001t0002g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2401-593A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172815011 | ||||||
chr3:172815039 | G | T | 1 | a0001c0001t0002g0205 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2401-565G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 22/24 | chr3 | 172815039 | ||||||
chr3:172815935 | G | A | 24 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0015others(21): Show | 34 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2508+224G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 23/24 | chr3 | 172815935 | ||||||
chr3:172815945 | C | G | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(15): Show | 21 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.2508+234C>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 23/24 | chr3 | 172815945 | ||||||
chr3:172816116 | T | G | 1 | a0001c0001t0002g0163 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2508+405T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 23/24 | chr3 | 172816116 | ||||||
chr3:172816129 | T | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(12): Show | 21 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.2508+418T>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 23/24 | chr3 | 172816129 | ||||||
chr3:172816638 | C | T | 166 | a0001c0001t0001g0093a0001c0001t0002g0001a0001c0001t0002g0004others(163): Show | 186 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.2509-53C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 23/24 | chr3 | 172816638 | ||||||
chr3:172816869 | C | T | 39 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(36): Show | 46 | HG00621.hp2 HG00673.hp1 HG02132.hp2 others(43): Show |
intron_variant | MODIFIER | c.2655+32C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172816869 | ||||||
chr3:172816939 | A | T | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2655+102A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172816939 | ||||||
chr3:172816997 | A | G | 2 | a0001c0001t0004g0107a0001c0001t0004g0108 | 2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2655+160A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172816997 | ||||||
chr3:172817187 | A | C | 2 | a0001c0001t0006g0123a0001c0001t0006g0124 | 2 | HG00741.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2655+350A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172817187 | ||||||
chr3:172817256 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2655+419C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172817256 | ||||||
chr3:172817326 | A | C | 102 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(99): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2655+489A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172817326 | ||||||
chr3:172817444 | C | T | 20 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(17): Show | 21 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.2655+607C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172817444 | ||||||
chr3:172817480 | A | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.2655+643A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172817480 | ||||||
chr3:172817748 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2655+911A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172817748 | ||||||
chr3:172817767 | C | T | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.2655+930C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172817767 | ||||||
chr3:172818145 | A | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0048others(4): Show | 9 | HG01433.hp2 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2655+1308A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172818145 | ||||||
chr3:172818195 | A | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.2655+1358A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172818195 | ||||||
chr3:172818240 | A | G | 101 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(98): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2655+1403A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172818240 | ||||||
chr3:172818250 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2655+1413A>C | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172818250 | ||||||
chr3:172818340 | A | T | 17 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0023others(14): Show | 25 | HG00280.hp1 HG00323.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.2655+1503A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172818340 | ||||||
chr3:172818405 | A | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0048others(4): Show | 9 | HG01433.hp2 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2655+1568A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172818405 | ||||||
chr3:172818503 | A | G | 21 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(18): Show | 22 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.2656-1645A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172818503 | ||||||
chr3:172818573 | A | G | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2656-1575A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172818573 | ||||||
chr3:172818660 | G | A | 20 | a0001c0001t0004g0030a0001c0001t0004g0244a0001c0001t0004g0245others(17): Show | 21 | HG01255.hp1 HG02486.hp2 HG02572.hp2 others(18): Show |
intron_variant | MODIFIER | c.2656-1488G>A | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172818660 | ||||||
chr3:172818823 | A | T | 1 | a0001c0001t0011g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2656-1325A>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172818823 | ||||||
chr3:172819169 | A | G | 1 | a0001c0001t0002g0155 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2656-979A>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172819169 | ||||||
chr3:172819272 | A | AC | 60 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0029others(57): Show | 68 | HG00621.hp2 HG00673.hp1 HG01255.hp1 others(65): Show |
intron_variant | MODIFIER | c.2656-876_2656-875i others(3): Show |
ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172819272 | ||||||
chr3:172819686 | C | T | 4 | a0001c0001t0007g0019a0001c0001t0007g0083a0001c0001t0007g0084others(1): Show | 5 | HG01192.hp2 HG03688.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.2656-462C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172819686 | ||||||
chr3:172819869 | G | T | 1 | a0002c0003t0003g0095 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2656-279G>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172819869 | ||||||
chr3:172819878 | C | T | 102 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(99): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2656-270C>T | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172819878 | ||||||
chr3:172820060 | T | G | 101 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0026others(98): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.2656-88T>G | ECT2 | ENSG00000114346.14 | transcript | ENST00000392692.8 | protein_coding | 24/24 | chr3 | 172820060 |