Item | Value |
---|---|
geneid | 1889 |
ensemblid | ENSG00000117298.16 |
hgncid | 3146 |
symbol | ECE1 |
name | endothelin converting enzyme 1 |
refseq_nuc | NM_001397.3 |
refseq_prot | NP_001388.1 |
ensembl_nuc | ENST00000374893.11 |
ensembl_prot | ENSP00000364028.6 |
mane_status | MANE Select |
chr | chr1 |
start | 21217250 |
end | 21290463 |
strand | - |
ver | v1.2 |
region | chr1:21217250-21290463 |
region5000 | chr1:21212250-21295463 |
regionname0 | ECE1_chr1_21217250_21290463 |
regionname5000 | ECE1_chr1_21212250_21295463 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 770 | 290 | 91 | 50 | 103 | 12 | 32 | 73 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0002 | 0/0 | 770 | 6 | 0 | 2 | 0 | 2 | 2 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0003 | 0/0 | 770 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0004 | 0/0 | 770 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0005 | 0/0 | 770 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0006 | 0/0 | 770 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0007 | 0/0 | 770 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0008 | 0/0 | 770 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0009 | 0/0 | 770 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0010 | 0/0 | 770 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2313 | 206 | 50 | 30 | 87 | 8 | 29 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0002 | 0/0 | 2313 | 39 | 35 | 4 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0003 | 0/0 | 2313 | 39 | 3 | 16 | 13 | 4 | 3 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0004 | 0/0 | 2313 | 4 | 0 | 1 | 0 | 1 | 2 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0005 | 0/0 | 2313 | 2 | 0 | 0 | 2 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0006 | 0/0 | 2313 | 2 | 0 | 1 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0007 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0008 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0009 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0010 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0011 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0012 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0013 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0014 | 0/0 | 2313 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0015 | 0/0 | 2313 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0016 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0017 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
c0018 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2755 | 125 | 18 | 26 | 60 | 3 | 17 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0002 | 0/0 | 2755 | 53 | 18 | 16 | 12 | 3 | 4 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0003 | 0/1 | 2755 | 43 | 7 | 2 | 21 | 3 | 9 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0004 | 0/0 | 2755 | 22 | 19 | 3 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0005 | 0/0 | 2755 | 8 | 7 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0006 | 0/0 | 2755 | 7 | 0 | 1 | 0 | 3 | 3 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0007 | 0/0 | 2755 | 7 | 6 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0008 | 0/0 | 2753 | 4 | 0 | 0 | 4 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0009 | 0/0 | 2755 | 3 | 3 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0010 | 0/0 | 2755 | 2 | 2 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0011 | 0/0 | 2755 | 2 | 2 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0012 | 0/0 | 2755 | 2 | 2 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0013 | 0/0 | 2755 | 2 | 0 | 2 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0014 | 0/0 | 2755 | 2 | 2 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0015 | 0/0 | 2755 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0016 | 0/0 | 2755 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0017 | 0/0 | 2755 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0018 | 0/0 | 2755 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0019 | 0/0 | 2755 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0020 | 0/0 | 2755 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0021 | 0/0 | 2755 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0022 | 0/0 | 2755 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0023 | 0/0 | 2755 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0024 | 0/0 | 2755 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0025 | 0/0 | 2755 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0026 | 0/0 | 2755 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0027 | 0/0 | 2783 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0028 | 0/0 | 2755 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0029 | 0/0 | 2755 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0030 | 0/0 | 2755 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0031 | 0/0 | 2755 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0032 | 0/0 | 2755 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0033 | 0/0 | 2753 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0034 | 0/0 | 2755 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0035 | 0/0 | 2755 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
t0036 | 0/0 | 2755 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2313 | 206 | 50 | 30 | 87 | 8 | 29 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0001c0002 | 0/0 | 2313 | 39 | 35 | 4 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0001c0003 | 0/0 | 2313 | 39 | 3 | 16 | 13 | 4 | 3 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0001c0005 | 0/0 | 2313 | 2 | 0 | 0 | 2 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0001c0007 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0001c0008 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0001c0013 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0001c0017 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0002c0004 | 0/0 | 2313 | 4 | 0 | 1 | 0 | 1 | 2 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0002c0006 | 0/0 | 2313 | 2 | 0 | 1 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0003c0016 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0004c0014 | 0/0 | 2313 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0005c0010 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0006c0011 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0007c0012 | 0/0 | 2313 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0008c0015 | 0/0 | 2313 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0009c0009 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 | |
a0010c0018 | 0/0 | 2313 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5067 | 110 | 16 | 20 | 53 | 3 | 17 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0002 | 0/0 | 5067 | 27 | 16 | 6 | 3 | 1 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0003 | 0/1 | 5067 | 38 | 7 | 1 | 19 | 1 | 9 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0004 | 0/0 | 5067 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0006 | 0/0 | 5067 | 3 | 0 | 0 | 0 | 2 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0007 | 0/0 | 5067 | 7 | 6 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0008 | 0/0 | 5065 | 4 | 0 | 0 | 4 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0013 | 0/0 | 5067 | 2 | 0 | 2 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0018 | 0/0 | 5067 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0019 | 0/0 | 5067 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0022 | 0/0 | 5067 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0024 | 0/0 | 5067 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0025 | 0/0 | 5067 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0026 | 0/0 | 5067 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0027 | 0/0 | 5095 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0028 | 0/0 | 5067 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0029 | 0/0 | 5067 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0030 | 0/0 | 5067 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0031 | 0/0 | 5067 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0032 | 0/0 | 5067 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0033 | 0/0 | 5065 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0001t0035 | 0/0 | 5067 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0002t0004 | 0/0 | 5067 | 19 | 16 | 3 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0002t0005 | 0/0 | 5067 | 8 | 7 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0002t0009 | 0/0 | 5067 | 3 | 3 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0002t0010 | 0/0 | 5067 | 2 | 2 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0002t0011 | 0/0 | 5067 | 2 | 2 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0002t0012 | 0/0 | 5067 | 2 | 2 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0002t0014 | 0/0 | 5067 | 2 | 2 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0002t0034 | 0/0 | 5067 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0003t0001 | 0/0 | 5067 | 11 | 2 | 5 | 4 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0003t0002 | 0/0 | 5067 | 24 | 1 | 10 | 8 | 2 | 3 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0003t0003 | 0/0 | 5067 | 3 | 0 | 1 | 0 | 2 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0003t0036 | 0/0 | 5067 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0005t0001 | 0/0 | 5067 | 2 | 0 | 0 | 2 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0007t0004 | 0/0 | 5067 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0008t0002 | 0/0 | 5067 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0013t0004 | 0/0 | 5067 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0001c0017t0020 | 0/0 | 5067 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0002c0004t0006 | 0/0 | 5067 | 4 | 0 | 1 | 0 | 1 | 2 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0002c0006t0015 | 0/0 | 5067 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0002c0006t0016 | 0/0 | 5067 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0003c0016t0023 | 0/0 | 5067 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0004c0014t0021 | 0/0 | 5067 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0005c0010t0001 | 0/0 | 5067 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0006c0011t0003 | 0/0 | 5067 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0007c0012t0003 | 0/0 | 5067 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0008c0015t0001 | 0/0 | 5067 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0009c0009t0002 | 0/0 | 5067 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
a0010c0018t0017 | 0/0 | 5067 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | copy fasta | chr1 | 21212250 | 21295463 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0006g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0006g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0006g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0007g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0007g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0013g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0013g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0018g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0019g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0022g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0024g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0025g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0026g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0027g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0028g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0029g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0030g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0031g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0032g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0033g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0001t0035g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0005g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0009g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0010g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0010g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0011g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0011g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0012g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0012g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0014g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0014g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0002t0034g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0003t0036g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0005t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0005t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0007t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0008t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0013t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0001c0017t0020g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0002c0004t0006g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0002c0004t0006g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0002c0004t0006g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0002c0006t0015g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0002c0006t0016g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0003c0016t0023g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0004c0014t0021g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0005c0010t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0006c0011t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0007c0012t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0008c0015t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0009c0009t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
a0010c0018t0017g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0004 | t0006 | g0002 | EUR | GBR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00140 | hp2 | a0001 | c0003 | t0002 | g0080 | EUR | GBR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0114 | EUR | FIN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00323 | hp2 | a0001 | c0001 | t0006 | g0015 | EUR | FIN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | CHS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00558 | hp1 | a0001 | c0003 | t0002 | g0082 | EAS | CHS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | CHS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00621 | hp2 | a0001 | c0001 | t0029 | g0069 | EAS | CHS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00639 | hp1 | a0001 | c0003 | t0002 | g0151 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | CHS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0208 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0197 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01069 | hp1 | a0001 | c0002 | t0005 | g0243 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01069 | hp2 | a0001 | c0002 | t0004 | g0249 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01070 | hp2 | a0004 | c0014 | t0021 | g0141 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01071 | hp1 | a0001 | c0002 | t0004 | g0250 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01074 | hp2 | a0002 | c0006 | t0015 | g0011 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01099 | hp2 | a0001 | c0001 | t0013 | g0017 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01106 | hp1 | a0001 | c0003 | t0003 | g0099 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01109 | hp1 | a0001 | c0003 | t0002 | g0171 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01109 | hp2 | a0001 | c0002 | t0004 | g0084 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01167 | hp2 | a0001 | c0001 | t0007 | g0275 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01175 | hp2 | a0001 | c0003 | t0002 | g0180 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01255 | hp1 | a0001 | c0003 | t0002 | g0144 | AMR | CLM | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01255 | hp2 | a0002 | c0004 | t0006 | g0013 | AMR | CLM | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01258 | hp1 | a0001 | c0003 | t0002 | g0120 | AMR | CLM | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0048 | AMR | CLM | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01515 | hp1 | a0001 | c0003 | t0003 | g0042 | EUR | IBS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01515 | hp2 | a0001 | c0001 | t0027 | g0115 | EUR | IBS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01516 | hp2 | a0002 | c0006 | t0016 | g0172 | EUR | IBS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01517 | hp2 | a0001 | c0003 | t0003 | g0041 | EUR | IBS | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01884 | hp2 | a0001 | c0017 | t0020 | g0235 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01928 | hp1 | a0001 | c0003 | t0002 | g0019 | AMR | PEL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01934 | hp1 | a0001 | c0003 | t0002 | g0066 | AMR | PEL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01952 | hp1 | a0001 | c0003 | t0002 | g0050 | AMR | PEL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01975 | hp1 | a0008 | c0015 | t0001 | g0030 | AMR | PEL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG01975 | hp2 | a0001 | c0003 | t0002 | g0085 | AMR | PEL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02004 | hp1 | a0001 | c0003 | t0002 | g0049 | AMR | PEL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02055 | hp2 | a0001 | c0002 | t0004 | g0291 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02132 | hp2 | a0001 | c0001 | t0026 | g0134 | EAS | KHV | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02135 | hp2 | a0001 | c0001 | t0032 | g0199 | EAS | KHV | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02145 | hp1 | a0001 | c0002 | t0004 | g0266 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0288 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02148 | hp1 | a0001 | c0001 | t0013 | g0179 | AMR | PEL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02155 | hp1 | a0001 | c0003 | t0036 | g0081 | EAS | CDX | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02165 | hp1 | a0007 | c0012 | t0003 | g0054 | EAS | CDX | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02257 | hp2 | a0001 | c0002 | t0005 | g0205 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02258 | hp2 | a0001 | c0003 | t0001 | g0188 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02280 | hp2 | a0001 | c0002 | t0014 | g0229 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02523 | hp2 | a0006 | c0011 | t0003 | g0135 | EAS | KHV | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02615 | hp2 | a0001 | c0003 | t0002 | g0139 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02622 | hp1 | a0001 | c0002 | t0004 | g0285 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02622 | hp2 | a0001 | c0001 | t0028 | g0294 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02630 | hp2 | a0001 | c0002 | t0004 | g0256 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02647 | hp2 | a0001 | c0002 | t0012 | g0108 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02683 | hp2 | a0002 | c0004 | t0006 | g0002 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02698 | hp1 | a0002 | c0004 | t0006 | g0010 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0161 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02717 | hp1 | a0001 | c0002 | t0005 | g0104 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02723 | hp2 | a0001 | c0007 | t0004 | g0215 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02809 | hp1 | a0001 | c0002 | t0034 | g0260 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02809 | hp2 | a0001 | c0001 | t0024 | g0210 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02818 | hp1 | a0001 | c0002 | t0009 | g0239 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02818 | hp2 | a0001 | c0002 | t0004 | g0293 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02895 | hp1 | a0001 | c0002 | t0011 | g0016 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02896 | hp1 | a0001 | c0002 | t0004 | g0009 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02896 | hp2 | a0001 | c0001 | t0031 | g0101 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02897 | hp1 | a0001 | c0002 | t0004 | g0009 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02922 | hp1 | a0001 | c0002 | t0009 | g0274 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02965 | hp1 | a0001 | c0002 | t0004 | g0214 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02965 | hp2 | a0001 | c0001 | t0007 | g0244 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02970 | hp2 | a0001 | c0002 | t0004 | g0278 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0245 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03017 | hp2 | a0001 | c0003 | t0002 | g0051 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0246 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | MSL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0273 | AFR | MSL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03130 | hp1 | a0001 | c0002 | t0012 | g0234 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03130 | hp2 | a0001 | c0013 | t0004 | g0268 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03139 | hp1 | a0009 | c0009 | t0002 | g0270 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03139 | hp2 | a0001 | c0002 | t0004 | g0259 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03209 | hp2 | a0010 | c0018 | t0017 | g0236 | AFR | MSL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03225 | hp1 | a0001 | c0002 | t0014 | g0230 | AFR | MSL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03225 | hp2 | a0001 | c0002 | t0010 | g0213 | AFR | MSL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03453 | hp1 | a0001 | c0002 | t0010 | g0264 | AFR | MSL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03486 | hp1 | a0001 | c0002 | t0011 | g0241 | AFR | MSL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03516 | hp1 | a0001 | c0001 | t0035 | g0097 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03540 | hp1 | a0001 | c0002 | t0004 | g0098 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | GWD | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | MSL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03579 | hp2 | a0001 | c0002 | t0004 | g0263 | AFR | MSL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03669 | hp1 | a0001 | c0001 | t0022 | g0149 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0211 | SAS | STU | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | BEB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0033 | SAS | BEB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03927 | hp1 | a0001 | c0003 | t0002 | g0209 | SAS | BEB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0121 | SAS | STU | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0102 | SAS | STU | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG04204 | hp1 | a0001 | c0001 | t0006 | g0014 | SAS | STU | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0062 | SAS | STU | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | STU | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18522 | hp1 | a0001 | c0002 | t0004 | g0267 | AFR | YRI | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | CHB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18906 | hp1 | a0001 | c0002 | t0005 | g0242 | AFR | YRI | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | YRI | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18941 | hp1 | a0001 | c0005 | t0001 | g0044 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18947 | hp1 | a0001 | c0005 | t0001 | g0043 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18947 | hp2 | a0001 | c0001 | t0008 | g0204 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18951 | hp2 | a0001 | c0003 | t0002 | g0083 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18954 | hp1 | a0001 | c0001 | t0033 | g0091 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18954 | hp2 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18959 | hp2 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18960 | hp1 | a0001 | c0001 | t0008 | g0052 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18960 | hp2 | a0001 | c0001 | t0008 | g0247 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18969 | hp1 | a0001 | c0001 | t0030 | g0056 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18970 | hp2 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18994 | hp1 | a0001 | c0003 | t0002 | g0022 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19005 | hp1 | a0001 | c0003 | t0002 | g0219 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19010 | hp1 | a0001 | c0001 | t0019 | g0192 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | LWK | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19043 | hp1 | a0001 | c0002 | t0005 | g0231 | AFR | LWK | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | LWK | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19057 | hp1 | a0001 | c0003 | t0002 | g0193 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19060 | hp1 | a0001 | c0001 | t0008 | g0248 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19063 | hp2 | a0001 | c0003 | t0001 | g0216 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19065 | hp2 | a0001 | c0003 | t0002 | g0046 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19068 | hp1 | a0001 | c0003 | t0002 | g0021 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19078 | hp1 | a0001 | c0001 | t0025 | g0207 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19078 | hp2 | a0005 | c0010 | t0001 | g0073 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19079 | hp1 | a0001 | c0008 | t0002 | g0194 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19090 | hp1 | a0001 | c0003 | t0002 | g0195 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19090 | hp2 | a0001 | c0001 | t0018 | g0055 | EAS | JPT | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0145 | AFR | YRI | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA19240 | hp2 | a0001 | c0002 | t0005 | g0201 | AFR | YRI | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ASW | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | ASW | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0106 | EUR | TSI | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA20805 | hp1 | a0001 | c0001 | t0006 | g0012 | EUR | TSI | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA20805 | hp2 | a0001 | c0003 | t0002 | g0164 | EUR | TSI | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | GIH | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0103 | SAS | GIH | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02109 | hp2 | a0001 | c0002 | t0005 | g0237 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02486 | hp2 | a0001 | c0002 | t0004 | g0265 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0289 | AFR | ACB | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03471 | hp1 | a0001 | c0002 | t0004 | g0257 | AFR | MSL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG03471 | hp2 | a0003 | c0016 | t0023 | g0233 | AFR | MSL | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | USA | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
HG06807 | hp2 | a0001 | c0002 | t0004 | g0281 | AFR | USA | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | USA | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA20300 | hp2 | a0001 | c0002 | t0005 | g0232 | AFR | USA | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
NA21309 | hp2 | a0001 | c0002 | t0009 | g0227 | AFR | LWK | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0160 | REF | REF | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0127 | REF | REF | ECE1_chr1_21212250_21295463 | ECE1 | chr1 | 21212250 | 21295463 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:21219981 | G | C | 1 | a0007 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.2287C>G | p.Pro763Ala | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 2336/5067 | 2287/2313 | 763/770 | chr1 | 21219981 | ||
chr1:21225330 | C | T | 1 | a0006 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1960G>A | p.Val654Met | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/19 | 2009/5067 | 1960/2313 | 654/770 | chr1 | 21225330 | ||
chr1:21225402 | A | T | 1 | a0005 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.1888T>A | p.Trp630Arg | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/19 | 1937/5067 | 1888/2313 | 630/770 | chr1 | 21225402 | ||
chr1:21233576 | T | C | 1 | a0008 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.1652A>G | p.Lys551Arg | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/19 | 1701/5067 | 1652/2313 | 551/770 | chr1 | 21233576 | ||
chr1:21238138 | C | T | 1 | a0004 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.1385G>A | p.Ser462Asn | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 11/19 | 1434/5067 | 1385/2313 | 462/770 | chr1 | 21238138 | ||
chr1:21247324 | T | C | 1 | a0003 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.1060A>G | p.Thr354Ala | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/19 | 1109/5067 | 1060/2313 | 354/770 | chr1 | 21247324 | ||
chr1:21247351 | C | T | 1 | a0009 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.1033G>A | p.Ala345Thr | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/19 | 1082/5067 | 1033/2313 | 345/770 | chr1 | 21247351 | ||
chr1:21247362 | G | A | 1 | a0002 | 6 | HG00140.hp1 HG01074.hp2 HG01255.hp2 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.1022C>T | p.Thr341Ile | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/19 | 1071/5067 | 1022/2313 | 341/770 | chr1 | 21247362 | ||
chr1:21260315 | T | C | 1 | a0010 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.571A>G | p.Ile191Val | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/19 | 620/5067 | 571/2313 | 191/770 | chr1 | 21260315 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:21221762 | G | A | 1 | a0001c0005 | 2 | NA18941.hp1 NA18947.hp1 |
synonymous_variant | LOW | c.2121C>T | p.Phe707Phe | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/19 | 2170/5067 | 2121/2313 | 707/770 | chr1 | 21221762 | ||
chr1:21233587 | A | G | 6 | a0001c0002a0001c0007a0001c0013others(3): Show | 45 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
synonymous_variant | LOW | c.1641T>C | p.Asp547Asp | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/19 | 1690/5067 | 1641/2313 | 547/770 | chr1 | 21233587 | ||
chr1:21235850 | G | A | 1 | a0001c0013 | 1 | HG03130.hp2 | splice_region_variant&synonymous_variant | LOW | c.1566C>T | p.Asp522Asp | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/19 | 1615/5067 | 1566/2313 | 522/770 | chr1 | 21235850 | ||
chr1:21247229 | G | A | 4 | a0001c0003a0001c0008a0004c0014others(1): Show | 42 | HG00140.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
synonymous_variant | LOW | c.1155C>T | p.Thr385Thr | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/19 | 1204/5067 | 1155/2313 | 385/770 | chr1 | 21247229 | ||
chr1:21257531 | G | A | 1 | a0001c0017 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.822C>T | p.Asn274Asn | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/19 | 871/5067 | 822/2313 | 274/770 | chr1 | 21257531 | ||
chr1:21260382 | C | T | 2 | a0001c0007a0001c0008 | 2 | HG02723.hp2 NA19079.hp1 |
synonymous_variant | LOW | c.504G>A | p.Thr168Thr | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/19 | 553/5067 | 504/2313 | 168/770 | chr1 | 21260382 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:21217278 | A | C | 1 | a0001c0001t0030 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2677T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 2677 | chr1 | 21217278 | |||||
chr1:21217330 | T | C | 2 | a0002c0006t0015a0002c0006t0016 | 2 | HG01074.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2625A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 2625 | chr1 | 21217330 | |||||
chr1:21217337 | C | G | 1 | a0001c0001t0033 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2618G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 2618 | chr1 | 21217337 | |||||
chr1:21217468 | T | G | 1 | a0001c0001t0033 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2487A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 2487 | chr1 | 21217468 | |||||
chr1:21217574 | C | A | 1 | a0001c0001t0007 | 7 | HG01167.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2381G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 2381 | chr1 | 21217574 | |||||
chr1:21217577 | G | A | 1 | a0001c0001t0031 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2378C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 2378 | chr1 | 21217577 | |||||
chr1:21217581 | G | C | 15 | a0001c0001t0004a0001c0001t0007a0001c0001t0024others(12): Show | 50 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2374C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 2374 | chr1 | 21217581 | |||||
chr1:21217630 | G | A | 1 | a0001c0001t0028 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2325C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 2325 | chr1 | 21217630 | |||||
chr1:21217709 | C | CTCTATGT others(21): Show |
1 | a0001c0001t0027 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2245_*2246insAGCC others(24): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 2245 | chr1 | 21217709 | |||||
chr1:21217730 | C | A | 11 | a0001c0001t0003a0001c0001t0018a0001c0001t0022others(8): Show | 51 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2225G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 2225 | chr1 | 21217730 | |||||
chr1:21217789 | A | G | 1 | a0001c0001t0026 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2166T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 2166 | chr1 | 21217789 | |||||
chr1:21217872 | C | T | 1 | a0001c0001t0029 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2083G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 2083 | chr1 | 21217872 | |||||
chr1:21217954 | G | A | 11 | a0001c0001t0003a0001c0001t0018a0001c0001t0022others(8): Show | 51 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2001C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 2001 | chr1 | 21217954 | |||||
chr1:21218009 | C | T | 5 | a0001c0001t0004a0001c0002t0004a0001c0002t0034others(2): Show | 23 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1946G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 1946 | chr1 | 21218009 | |||||
chr1:21218012 | G | A | 3 | a0001c0002t0011a0002c0006t0015a0002c0006t0016 | 4 | HG01074.hp2 HG01516.hp2 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1943C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 1943 | chr1 | 21218012 | |||||
chr1:21218108 | C | T | 28 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(25): Show | 104 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1847G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 1847 | chr1 | 21218108 | |||||
chr1:21218175 | C | G | 3 | a0001c0002t0011a0002c0006t0015a0002c0006t0016 | 4 | HG01074.hp2 HG01516.hp2 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1780G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 1780 | chr1 | 21218175 | |||||
chr1:21218233 | C | G | 1 | a0001c0002t0010 | 2 | HG03225.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1722G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 1722 | chr1 | 21218233 | |||||
chr1:21218242 | C | T | 10 | a0001c0001t0003a0001c0001t0018a0001c0001t0022others(7): Show | 49 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1713G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 1713 | chr1 | 21218242 | |||||
chr1:21218298 | T | C | 35 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(32): Show | 160 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*1657A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 1657 | chr1 | 21218298 | |||||
chr1:21218571 | G | A | 2 | a0001c0001t0007a0010c0018t0017 | 8 | HG01167.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1384C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 1384 | chr1 | 21218571 | |||||
chr1:21218611 | G | C | 1 | a0001c0001t0022 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1344C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 1344 | chr1 | 21218611 | |||||
chr1:21218747 | C | T | 1 | a0001c0001t0025 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1208G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 1208 | chr1 | 21218747 | |||||
chr1:21218803 | C | T | 1 | a0001c0001t0013 | 2 | HG01099.hp2 HG02148.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1152G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 1152 | chr1 | 21218803 | |||||
chr1:21218834 | G | A | 1 | a0001c0002t0009 | 3 | HG02818.hp1 HG02922.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1121C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 1121 | chr1 | 21218834 | |||||
chr1:21219089 | T | C | 2 | a0001c0002t0012a0001c0017t0020 | 3 | HG01884.hp2 HG02647.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*866A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 866 | chr1 | 21219089 | |||||
chr1:21219224 | CAG | C | 2 | a0001c0001t0008a0001c0001t0033 | 5 | NA18947.hp2 NA18954.hp1 NA18960.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*729_*730delCT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 729 | chr1 | 21219224 | |||||
chr1:21219240 | G | C | 2 | a0002c0006t0015a0002c0006t0016 | 2 | HG01074.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*715C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 715 | chr1 | 21219240 | |||||
chr1:21219285 | A | G | 18 | a0001c0001t0004a0001c0001t0007a0001c0001t0024others(15): Show | 54 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*670T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 670 | chr1 | 21219285 | |||||
chr1:21219396 | G | T | 1 | a0001c0001t0022 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*559C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 559 | chr1 | 21219396 | |||||
chr1:21219540 | A | T | 1 | a0004c0014t0021 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*415T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 415 | chr1 | 21219540 | |||||
chr1:21219623 | A | G | 1 | a0001c0017t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*332T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 332 | chr1 | 21219623 | |||||
chr1:21219653 | T | C | 1 | a0001c0002t0034 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*302A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 302 | chr1 | 21219653 | |||||
chr1:21219659 | C | T | 1 | a0001c0001t0019 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*296G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 296 | chr1 | 21219659 | |||||
chr1:21219787 | G | A | 1 | a0001c0001t0035 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*168C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 168 | chr1 | 21219787 | |||||
chr1:21219821 | C | T | 6 | a0001c0001t0007a0001c0001t0018a0001c0002t0005others(3): Show | 22 | HG01069.hp1 HG01167.hp2 HG02109.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*134G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 134 | chr1 | 21219821 | |||||
chr1:21219863 | G | T | 2 | a0002c0006t0015a0002c0006t0016 | 2 | HG01074.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*92C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 92 | chr1 | 21219863 | |||||
chr1:21219946 | G | A | 1 | a0001c0003t0036 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 19/19 | 9 | chr1 | 21219946 | |||||
chr1:21290439 | G | T | 3 | a0001c0001t0006a0002c0004t0006a0002c0006t0015 | 8 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-25C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 1/19 | 25 | chr1 | 21290439 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:21220264 | G | A | 5 | a0001c0001t0001g0040a0001c0003t0001g0216a0001c0003t0001g0217others(2): Show | 5 | NA18954.hp2 NA18959.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2137-133C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21220264 | ||||||
chr1:21220359 | G | C | 48 | a0001c0001t0004g0289a0001c0001t0007g0008a0001c0001t0007g0244others(45): Show | 50 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.2137-228C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21220359 | ||||||
chr1:21220468 | C | T | 1 | a0002c0004t0006g0010 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2137-337G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21220468 | ||||||
chr1:21220584 | G | A | 7 | a0001c0001t0003g0018a0001c0001t0003g0189a0001c0001t0003g0200others(4): Show | 7 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2137-453C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21220584 | ||||||
chr1:21220627 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2137-496A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21220627 | ||||||
chr1:21220653 | T | C | 3 | a0001c0002t0005g0104a0001c0002t0005g0231a0001c0002t0005g0232 | 3 | HG02717.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2137-522A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21220653 | ||||||
chr1:21220779 | G | A | 6 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(3): Show | 7 | HG01167.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.2137-648C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21220779 | ||||||
chr1:21220796 | C | T | 1 | a0001c0001t0035g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2137-665G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21220796 | ||||||
chr1:21221024 | G | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(22): Show | 27 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.2136+723C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21221024 | ||||||
chr1:21221120 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2136+627C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21221120 | ||||||
chr1:21221213 | G | A | 101 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0018others(98): Show | 105 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.2136+534C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21221213 | ||||||
chr1:21221226 | G | C | 3 | a0001c0002t0012g0108a0001c0002t0012g0234a0001c0017t0020g0235 | 3 | HG01884.hp2 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2136+521C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21221226 | ||||||
chr1:21221435 | G | T | 8 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(5): Show | 9 | HG01167.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136+312C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21221435 | ||||||
chr1:21221473 | G | A | 4 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(1): Show | 5 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2136+274C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21221473 | ||||||
chr1:21221575 | A | G | 41 | a0001c0001t0003g0004a0001c0001t0003g0007a0001c0001t0003g0028others(38): Show | 43 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.2136+172T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 18/18 | chr1 | 21221575 | ||||||
chr1:21221975 | G | C | 1 | a0001c0001t0001g0040 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2041-133C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21221975 | ||||||
chr1:21222174 | G | GCA | 4 | a0001c0002t0011g0016a0001c0002t0011g0241a0002c0006t0015g0011others(1): Show | 4 | HG01074.hp2 HG01516.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2041-334_2041-333d others(4): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21222174 | ||||||
chr1:21222314 | C | T | 2 | a0001c0003t0001g0145a0001c0003t0001g0188 | 2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2041-472G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21222314 | ||||||
chr1:21222841 | C | CA | 83 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0031others(80): Show | 83 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.2041-1000dupT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21222841 | ||||||
chr1:21222841 | C | CAA | 11 | a0001c0001t0002g0142a0001c0002t0009g0239a0001c0003t0002g0019others(8): Show | 11 | HG00558.hp1 HG01109.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2041-1001_2041-100 others(6): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21222841 | ||||||
chr1:21222841 | CA | C | 11 | a0001c0001t0002g0282a0001c0001t0002g0286a0001c0001t0002g0290others(8): Show | 11 | HG01099.hp1 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2041-1000delT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21222841 | ||||||
chr1:21223219 | T | C | 1 | a0001c0002t0005g0242 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2041-1377A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21223219 | ||||||
chr1:21223405 | C | A | 1 | a0001c0002t0011g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2041-1563G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21223405 | ||||||
chr1:21223753 | C | T | 1 | a0009c0009t0002g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2040+1497G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21223753 | ||||||
chr1:21223850 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2040+1400C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21223850 | ||||||
chr1:21223953 | A | C | 21 | a0001c0002t0004g0009a0001c0002t0004g0084a0001c0002t0004g0098others(18): Show | 22 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2040+1297T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21223953 | ||||||
chr1:21224326 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2040+924A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21224326 | ||||||
chr1:21224360 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2040+890T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21224360 | ||||||
chr1:21224459 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2040+791A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21224459 | ||||||
chr1:21224510 | G | T | 10 | a0001c0002t0005g0104a0001c0002t0005g0201a0001c0002t0005g0205others(7): Show | 10 | HG02257.hp2 HG02717.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2040+740C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21224510 | ||||||
chr1:21224620 | G | C | 7 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(4): Show | 8 | HG01167.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.2040+630C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21224620 | ||||||
chr1:21224773 | C | T | 1 | a0001c0001t0035g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2040+477G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21224773 | ||||||
chr1:21224848 | C | T | 44 | a0001c0001t0001g0168a0001c0001t0003g0004a0001c0001t0003g0007others(41): Show | 46 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.2040+402G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21224848 | ||||||
chr1:21224964 | A | G | 151 | a0001c0001t0001g0168a0001c0001t0001g0187a0001c0001t0002g0067others(148): Show | 154 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.2040+286T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21224964 | ||||||
chr1:21225057 | A | C | 55 | a0001c0001t0002g0067a0001c0001t0002g0105a0001c0001t0002g0109others(52): Show | 55 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.2040+193T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21225057 | ||||||
chr1:21225112 | C | T | 3 | a0001c0002t0005g0104a0001c0002t0005g0231a0001c0002t0005g0232 | 3 | HG02717.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2040+138G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21225112 | ||||||
chr1:21225121 | G | A | 4 | a0001c0002t0011g0016a0001c0002t0011g0241a0002c0006t0015g0011others(1): Show | 4 | HG01074.hp2 HG01516.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2040+129C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21225121 | ||||||
chr1:21225135 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2040+115C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21225135 | ||||||
chr1:21225185 | T | C | 1 | a0001c0001t0035g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2040+65A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21225185 | ||||||
chr1:21225200 | G | C | 1 | a0001c0001t0007g0273 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2040+50C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21225200 | ||||||
chr1:21225225 | C | T | 4 | a0001c0002t0011g0016a0001c0002t0011g0241a0002c0006t0015g0011others(1): Show | 4 | HG01074.hp2 HG01516.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2040+25G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 17/18 | chr1 | 21225225 | ||||||
chr1:21225524 | C | T | 2 | a0001c0002t0004g0098a0001c0007t0004g0215 | 2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1850-84G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21225524 | ||||||
chr1:21225618 | G | A | 1 | a0009c0009t0002g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1850-178C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21225618 | ||||||
chr1:21225656 | C | T | 8 | a0001c0001t0001g0107a0001c0001t0001g0116a0001c0001t0001g0117others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1850-216G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21225656 | ||||||
chr1:21225695 | C | CT | 56 | a0001c0001t0002g0067a0001c0001t0002g0105a0001c0001t0002g0109others(53): Show | 56 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1850-256dupA | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21225695 | ||||||
chr1:21225695 | CT | C | 47 | a0001c0001t0001g0113a0001c0001t0001g0159a0001c0001t0007g0008others(44): Show | 49 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.1850-256delA | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21225695 | ||||||
chr1:21225733 | T | C | 49 | a0001c0001t0003g0288a0001c0001t0007g0008a0001c0001t0007g0244others(46): Show | 51 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.1850-293A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21225733 | ||||||
chr1:21225863 | G | GT | 7 | a0001c0001t0001g0025a0001c0001t0002g0114a0001c0001t0025g0207others(4): Show | 7 | HG00323.hp1 HG01884.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1850-424dupA | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21225863 | ||||||
chr1:21225888 | T | A | 1 | a0001c0001t0035g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1850-448A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21225888 | ||||||
chr1:21225955 | A | G | 1 | a0001c0001t0002g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1850-515T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21225955 | ||||||
chr1:21226285 | G | A | 1 | a0001c0001t0035g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1850-845C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21226285 | ||||||
chr1:21226298 | C | T | 1 | a0001c0001t0024g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1850-858G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21226298 | ||||||
chr1:21226422 | T | C | 1 | a0001c0001t0002g0228 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1849+737A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21226422 | ||||||
chr1:21226468 | T | A | 2 | a0001c0001t0001g0032a0001c0001t0008g0052 | 2 | NA18959.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1849+691A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21226468 | ||||||
chr1:21226471 | G | T | 36 | a0001c0001t0002g0067a0001c0001t0002g0105a0001c0001t0002g0114others(33): Show | 36 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1849+688C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21226471 | ||||||
chr1:21226530 | G | A | 1 | a0001c0001t0007g0275 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1849+629C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21226530 | ||||||
chr1:21226585 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1849+574C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21226585 | ||||||
chr1:21226687 | C | T | 111 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0002g0067others(108): Show | 113 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1849+472G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21226687 | ||||||
chr1:21226767 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1849+392G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21226767 | ||||||
chr1:21226787 | G | A | 2 | a0001c0001t0003g0177a0009c0009t0002g0270 | 2 | HG03139.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1849+372C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21226787 | ||||||
chr1:21226812 | G | A | 2 | a0002c0006t0015g0011a0002c0006t0016g0172 | 2 | HG01074.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1849+347C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21226812 | ||||||
chr1:21226921 | G | A | 2 | a0001c0002t0010g0213a0001c0002t0010g0264 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1849+238C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 16/18 | chr1 | 21226921 | ||||||
chr1:21227230 | G | T | 4 | a0001c0002t0011g0016a0001c0002t0011g0241a0002c0006t0015g0011others(1): Show | 4 | HG01074.hp2 HG01516.hp2 HG02895.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1782-4C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 15/18 | chr1 | 21227230 | ||||||
chr1:21227440 | T | C | 159 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0187others(156): Show | 163 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1782-214A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 15/18 | chr1 | 21227440 | ||||||
chr1:21227480 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1782-254G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 15/18 | chr1 | 21227480 | ||||||
chr1:21227506 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1782-280C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 15/18 | chr1 | 21227506 | ||||||
chr1:21227640 | C | T | 2 | a0002c0006t0015g0011a0002c0006t0016g0172 | 2 | HG01074.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1781+291G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 15/18 | chr1 | 21227640 | ||||||
chr1:21227826 | A | G | 291 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(288): Show | 301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.1781+105T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 15/18 | chr1 | 21227826 | ||||||
chr1:21228080 | C | T | 3 | a0001c0001t0001g0079a0001c0001t0006g0012a0001c0001t0006g0015 | 3 | HG00323.hp2 HG03831.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1671-39G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228080 | ||||||
chr1:21228111 | C | T | 1 | a0001c0002t0005g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1671-70G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228111 | ||||||
chr1:21228126 | G | A | 5 | a0001c0001t0001g0040a0001c0003t0001g0216a0001c0003t0001g0217others(2): Show | 5 | NA18954.hp2 NA18959.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671-85C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228126 | ||||||
chr1:21228223 | A | T | 7 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(4): Show | 8 | HG01167.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1671-182T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228223 | ||||||
chr1:21228226 | G | T | 2 | a0001c0002t0005g0201a0001c0002t0005g0205 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1671-185C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228226 | ||||||
chr1:21228245 | G | C | 2 | a0001c0001t0002g0109a0001c0001t0002g0190 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1671-204C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228245 | ||||||
chr1:21228316 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1671-275G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228316 | ||||||
chr1:21228418 | G | A | 1 | a0001c0001t0006g0012 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1671-377C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228418 | ||||||
chr1:21228533 | C | A | 1 | a0001c0001t0003g0162 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1671-492G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228533 | ||||||
chr1:21228623 | C | T | 47 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(44): Show | 49 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.1671-582G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228623 | ||||||
chr1:21228631 | C | CA | 8 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(5): Show | 9 | HG01167.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1671-591dupT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228631 | ||||||
chr1:21228649 | C | A | 4 | a0001c0002t0011g0016a0001c0002t0011g0241a0002c0006t0015g0011others(1): Show | 4 | HG01074.hp2 HG01516.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1671-608G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228649 | ||||||
chr1:21228696 | C | T | 5 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(2): Show | 6 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1671-655G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228696 | ||||||
chr1:21228832 | A | T | 1 | a0001c0001t0002g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1671-791T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228832 | ||||||
chr1:21228844 | C | CT | 6 | a0001c0001t0001g0225a0001c0002t0004g0266a0001c0002t0011g0016others(3): Show | 6 | HG01074.hp2 HG01516.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1671-804dupA | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228844 | ||||||
chr1:21228868 | G | GT | 293 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(290): Show | 303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.1671-828_1671-827i others(3): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228868 | ||||||
chr1:21228986 | C | T | 2 | a0001c0002t0011g0016a0001c0002t0011g0241 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1671-945G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21228986 | ||||||
chr1:21229014 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1671-973A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21229014 | ||||||
chr1:21229060 | C | T | 1 | a0009c0009t0002g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1671-1019G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21229060 | ||||||
chr1:21229083 | C | T | 4 | a0001c0002t0011g0016a0001c0002t0011g0241a0002c0006t0015g0011others(1): Show | 4 | HG01074.hp2 HG01516.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1671-1042G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21229083 | ||||||
chr1:21229239 | G | A | 5 | a0001c0001t0002g0109a0001c0001t0002g0190a0001c0001t0002g0271others(2): Show | 5 | HG00639.hp2 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1671-1198C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21229239 | ||||||
chr1:21229453 | T | C | 2 | a0001c0002t0011g0016a0001c0002t0011g0241 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1671-1412A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21229453 | ||||||
chr1:21229577 | A | T | 1 | a0001c0001t0007g0244 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1671-1536T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21229577 | ||||||
chr1:21229663 | T | C | 1 | a0001c0001t0002g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1671-1622A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21229663 | ||||||
chr1:21229665 | G | A | 46 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(43): Show | 48 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.1671-1624C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21229665 | ||||||
chr1:21229679 | A | G | 52 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0003g0004others(49): Show | 54 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1671-1638T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21229679 | ||||||
chr1:21229679 | A | T | 38 | a0001c0002t0004g0009a0001c0002t0004g0084a0001c0002t0004g0098others(35): Show | 39 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1671-1638T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21229679 | ||||||
chr1:21229720 | A | T | 1 | a0001c0001t0001g0065 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1671-1679T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21229720 | ||||||
chr1:21229936 | C | T | 2 | a0001c0002t0011g0016a0001c0002t0011g0241 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1671-1895G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21229936 | ||||||
chr1:21229940 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1671-1899C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21229940 | ||||||
chr1:21230131 | A | G | 46 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(43): Show | 48 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.1671-2090T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21230131 | ||||||
chr1:21230144 | G | A | 1 | a0001c0001t0028g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1671-2103C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21230144 | ||||||
chr1:21230303 | G | A | 1 | a0001c0003t0001g0208 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1671-2262C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21230303 | ||||||
chr1:21230394 | T | G | 43 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(40): Show | 45 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.1671-2353A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21230394 | ||||||
chr1:21230486 | C | A | 8 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(5): Show | 9 | HG01167.hp2 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1671-2445G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21230486 | ||||||
chr1:21230839 | T | C | 4 | a0001c0001t0008g0204a0001c0001t0008g0247a0001c0001t0008g0248others(1): Show | 4 | NA18947.hp2 NA18954.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670+2719A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21230839 | ||||||
chr1:21230855 | T | A | 1 | a0001c0003t0001g0222 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1670+2703A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21230855 | ||||||
chr1:21230914 | T | C | 4 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0003t0003g0041others(1): Show | 4 | HG01515.hp1 HG01517.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670+2644A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21230914 | ||||||
chr1:21230922 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1670+2636C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21230922 | ||||||
chr1:21231054 | C | T | 4 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(1): Show | 5 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670+2504G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21231054 | ||||||
chr1:21231198 | G | T | 38 | a0001c0002t0004g0009a0001c0002t0004g0084a0001c0002t0004g0098others(35): Show | 39 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1670+2360C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21231198 | ||||||
chr1:21231434 | C | T | 1 | a0001c0003t0002g0195 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1670+2124G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21231434 | ||||||
chr1:21231498 | T | C | 1 | a0001c0001t0003g0138 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1670+2060A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21231498 | ||||||
chr1:21231588 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1670+1970G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21231588 | ||||||
chr1:21231735 | A | G | 2 | a0001c0002t0011g0016a0001c0002t0011g0241 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1670+1823T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21231735 | ||||||
chr1:21231878 | C | A | 1 | a0001c0008t0002g0194 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1670+1680G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21231878 | ||||||
chr1:21231900 | C | T | 6 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(3): Show | 7 | HG01167.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1670+1658G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21231900 | ||||||
chr1:21231997 | C | A | 158 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0002g0067others(155): Show | 162 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.1670+1561G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21231997 | ||||||
chr1:21232139 | C | T | 3 | a0001c0002t0005g0237a0001c0002t0005g0242a0001c0002t0005g0243 | 3 | HG01069.hp1 HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1670+1419G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21232139 | ||||||
chr1:21232233 | C | A | 1 | a0001c0001t0001g0090 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1670+1325G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21232233 | ||||||
chr1:21232308 | C | T | 4 | a0001c0001t0001g0124a0001c0001t0001g0128a0001c0001t0001g0185others(1): Show | 4 | HG01106.hp2 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670+1250G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21232308 | ||||||
chr1:21232349 | A | G | 1 | a0003c0016t0023g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1670+1209T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21232349 | ||||||
chr1:21232384 | G | A | 8 | a0001c0002t0005g0201a0001c0002t0005g0205a0001c0002t0005g0237others(5): Show | 8 | HG01069.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1670+1174C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21232384 | ||||||
chr1:21232457 | T | C | 45 | a0001c0002t0004g0009a0001c0002t0004g0084a0001c0002t0004g0098others(42): Show | 46 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.1670+1101A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21232457 | ||||||
chr1:21232488 | C | A | 5 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0158others(2): Show | 5 | HG00609.hp2 HG02027.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1670+1070G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21232488 | ||||||
chr1:21232673 | AT | A | 22 | a0001c0002t0004g0009a0001c0002t0004g0084a0001c0002t0004g0214others(19): Show | 23 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1670+884delA | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21232673 | ||||||
chr1:21232686 | TTTTGAGA others(23): Show |
T | 1 | a0001c0001t0035g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1670+842_1670+871d others(32): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21232686 | ||||||
chr1:21232740 | C | T | 1 | a0001c0001t0035g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1670+818G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21232740 | ||||||
chr1:21232757 | C | T | 7 | a0001c0002t0011g0016a0001c0002t0011g0241a0001c0002t0014g0229others(4): Show | 7 | HG01074.hp2 HG01516.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1670+801G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21232757 | ||||||
chr1:21232826 | C | T | 2 | a0001c0002t0004g0265a0001c0002t0004g0266 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1670+732G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21232826 | ||||||
chr1:21232870 | G | T | 4 | a0001c0002t0011g0016a0001c0002t0011g0241a0002c0006t0015g0011others(1): Show | 4 | HG01074.hp2 HG01516.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670+688C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21232870 | ||||||
chr1:21233163 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1670+395A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21233163 | ||||||
chr1:21233166 | G | C | 1 | a0001c0002t0005g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1670+392C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21233166 | ||||||
chr1:21233168 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1670+390G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21233168 | ||||||
chr1:21233206 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1670+352G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21233206 | ||||||
chr1:21233209 | C | A | 158 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0002g0067others(155): Show | 162 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.1670+349G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21233209 | ||||||
chr1:21233448 | G | T | 35 | a0001c0001t0035g0097a0001c0002t0004g0009a0001c0002t0004g0084others(32): Show | 36 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1670+110C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21233448 | ||||||
chr1:21233550 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03195.hp2 | splice_region_variant&intron_variant | LOW | c.1670+8C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 14/18 | chr1 | 21233550 | ||||||
chr1:21233760 | G | C | 55 | a0001c0001t0002g0067a0001c0001t0002g0105a0001c0001t0002g0109others(52): Show | 55 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1567-99C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21233760 | ||||||
chr1:21233962 | A | G | 7 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(4): Show | 8 | HG01167.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1567-301T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21233962 | ||||||
chr1:21233981 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1567-320G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21233981 | ||||||
chr1:21233996 | T | C | 5 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(2): Show | 6 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1567-335A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21233996 | ||||||
chr1:21234012 | G | T | 8 | a0001c0002t0011g0016a0001c0002t0011g0241a0001c0002t0012g0108others(5): Show | 8 | HG01074.hp2 HG01516.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1567-351C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21234012 | ||||||
chr1:21234154 | A | G | 35 | a0001c0001t0035g0097a0001c0002t0004g0009a0001c0002t0004g0084others(32): Show | 36 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1567-493T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21234154 | ||||||
chr1:21234193 | G | A | 1 | a0010c0018t0017g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1567-532C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21234193 | ||||||
chr1:21234286 | C | T | 36 | a0001c0001t0002g0067a0001c0001t0002g0105a0001c0001t0002g0114others(33): Show | 36 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1567-625G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21234286 | ||||||
chr1:21234395 | G | C | 1 | a0001c0001t0035g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1567-734C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21234395 | ||||||
chr1:21234447 | C | T | 1 | a0010c0018t0017g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1567-786G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21234447 | ||||||
chr1:21234547 | C | T | 1 | a0001c0001t0006g0012 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1567-886G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21234547 | ||||||
chr1:21234687 | C | T | 39 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0251others(36): Show | 40 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.1567-1026G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21234687 | ||||||
chr1:21234922 | A | G | 4 | a0001c0002t0011g0016a0001c0002t0011g0241a0002c0006t0015g0011others(1): Show | 4 | HG01074.hp2 HG01516.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1566+928T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21234922 | ||||||
chr1:21234955 | T | G | 1 | a0001c0002t0004g0263 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1566+895A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21234955 | ||||||
chr1:21235004 | C | T | 1 | a0010c0018t0017g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1566+846G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21235004 | ||||||
chr1:21235100 | A | T | 1 | a0001c0013t0004g0268 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1566+750T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21235100 | ||||||
chr1:21235400 | A | C | 1 | a0001c0001t0001g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1566+450T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21235400 | ||||||
chr1:21235448 | A | AGGTGGTG others(5): Show |
1 | a0001c0002t0004g0267 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1566+390_1566+401d others(14): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21235448 | ||||||
chr1:21235544 | T | A | 1 | a0001c0003t0002g0046 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1566+306A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21235544 | ||||||
chr1:21235747 | A | G | 4 | a0001c0002t0011g0016a0001c0002t0011g0241a0002c0006t0015g0011others(1): Show | 4 | HG01074.hp2 HG01516.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1566+103T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21235747 | ||||||
chr1:21235803 | T | C | 1 | a0001c0002t0011g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1566+47A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21235803 | ||||||
chr1:21235821 | C | T | 1 | a0001c0002t0004g0293 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1566+29G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 13/18 | chr1 | 21235821 | ||||||
chr1:21235955 | T | A | 1 | a0001c0001t0002g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1489-28A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 12/18 | chr1 | 21235955 | ||||||
chr1:21236382 | G | T | 2 | a0001c0001t0001g0040a0001c0003t0001g0222 | 2 | NA18970.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1488+364C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 12/18 | chr1 | 21236382 | ||||||
chr1:21236383 | C | A | 2 | a0001c0001t0001g0040a0001c0003t0001g0222 | 2 | NA18970.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1488+363G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 12/18 | chr1 | 21236383 | ||||||
chr1:21236385 | T | A | 2 | a0001c0001t0001g0040a0001c0003t0001g0222 | 2 | NA18970.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1488+361A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 12/18 | chr1 | 21236385 | ||||||
chr1:21236425 | C | G | 50 | a0001c0001t0001g0187a0001c0001t0001g0238a0001c0001t0001g0240others(47): Show | 51 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.1488+321G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 12/18 | chr1 | 21236425 | ||||||
chr1:21236509 | C | T | 1 | a0001c0002t0005g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1488+237G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 12/18 | chr1 | 21236509 | ||||||
chr1:21236541 | C | T | 17 | a0001c0001t0002g0109a0001c0001t0002g0190a0001c0001t0002g0254others(14): Show | 17 | HG00639.hp2 HG01099.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1488+205G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 12/18 | chr1 | 21236541 | ||||||
chr1:21236557 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1488+189C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 12/18 | chr1 | 21236557 | ||||||
chr1:21236636 | C | T | 2 | a0001c0001t0003g0288a0001c0003t0003g0099 | 2 | HG01106.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1488+110G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 12/18 | chr1 | 21236636 | ||||||
chr1:21236670 | G | A | 8 | a0001c0001t0001g0040a0001c0003t0001g0005a0001c0003t0001g0048others(5): Show | 9 | HG00738.hp1 HG01358.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.1488+76C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 12/18 | chr1 | 21236670 | ||||||
chr1:21236709 | G | A | 1 | a0001c0001t0003g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1488+37C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 12/18 | chr1 | 21236709 | ||||||
chr1:21237091 | G | A | 21 | a0001c0002t0004g0009a0001c0002t0004g0084a0001c0002t0004g0098others(18): Show | 22 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1390-247C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 11/18 | chr1 | 21237091 | ||||||
chr1:21237120 | C | T | 2 | a0002c0006t0015g0011a0002c0006t0016g0172 | 2 | HG01074.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1390-276G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 11/18 | chr1 | 21237120 | ||||||
chr1:21237201 | C | T | 19 | a0001c0002t0004g0009a0001c0002t0004g0084a0001c0002t0004g0214others(16): Show | 20 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1390-357G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 11/18 | chr1 | 21237201 | ||||||
chr1:21237234 | C | T | 1 | a0001c0001t0027g0115 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1390-390G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 11/18 | chr1 | 21237234 | ||||||
chr1:21237235 | G | A | 3 | a0001c0002t0005g0104a0001c0002t0005g0231a0001c0002t0005g0232 | 3 | HG02717.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1390-391C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 11/18 | chr1 | 21237235 | ||||||
chr1:21237260 | G | A | 2 | a0001c0002t0005g0201a0001c0002t0005g0205 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1390-416C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 11/18 | chr1 | 21237260 | ||||||
chr1:21237597 | G | T | 1 | a0006c0011t0003g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1389+537C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 11/18 | chr1 | 21237597 | ||||||
chr1:21237691 | G | A | 1 | a0001c0001t0013g0179 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1389+443C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 11/18 | chr1 | 21237691 | ||||||
chr1:21237700 | T | C | 8 | a0001c0001t0001g0187a0001c0002t0012g0108a0001c0002t0012g0234others(5): Show | 8 | HG01192.hp2 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1389+434A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 11/18 | chr1 | 21237700 | ||||||
chr1:21237724 | C | T | 1 | a0001c0001t0003g0062 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1389+410G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 11/18 | chr1 | 21237724 | ||||||
chr1:21237740 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1389+394G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 11/18 | chr1 | 21237740 | ||||||
chr1:21238001 | T | C | 1 | a0001c0001t0035g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1389+133A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 11/18 | chr1 | 21238001 | ||||||
chr1:21238270 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1279-26C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21238270 | ||||||
chr1:21238367 | C | T | 2 | a0001c0003t0002g0164a0004c0014t0021g0141 | 2 | HG01070.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1279-123G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21238367 | ||||||
chr1:21238394 | G | A | 2 | a0002c0006t0015g0011a0002c0006t0016g0172 | 2 | HG01074.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1279-150C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21238394 | ||||||
chr1:21238477 | T | C | 1 | a0001c0001t0006g0015 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1279-233A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21238477 | ||||||
chr1:21238700 | G | A | 5 | a0001c0001t0001g0040a0001c0003t0001g0216a0001c0003t0001g0217others(2): Show | 5 | NA18954.hp2 NA18959.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-456C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21238700 | ||||||
chr1:21238738 | G | A | 1 | a0001c0002t0004g0257 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1279-494C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21238738 | ||||||
chr1:21238857 | G | A | 1 | a0001c0001t0003g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1279-613C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21238857 | ||||||
chr1:21238877 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1279-633T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21238877 | ||||||
chr1:21238971 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1279-727A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21238971 | ||||||
chr1:21238998 | A | AT | 13 | a0001c0001t0001g0094a0001c0001t0001g0187a0001c0001t0003g0202others(10): Show | 13 | HG01074.hp2 HG01192.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.1279-755dupA | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21238998 | ||||||
chr1:21238998 | A | T | 2 | a0001c0001t0003g0173a0001c0001t0003g0174 | 2 | NA18747.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1279-754T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21238998 | ||||||
chr1:21239214 | C | T | 1 | a0001c0001t0035g0097 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1279-970G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21239214 | ||||||
chr1:21239265 | G | A | 1 | a0001c0001t0007g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1279-1021C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21239265 | ||||||
chr1:21239297 | C | T | 2 | a0002c0006t0015g0011a0002c0006t0016g0172 | 2 | HG01074.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1279-1053G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21239297 | ||||||
chr1:21239298 | G | A | 2 | a0001c0001t0003g0163a0001c0001t0003g0177 | 2 | NA18951.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1279-1054C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21239298 | ||||||
chr1:21239368 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1279-1124G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21239368 | ||||||
chr1:21239394 | C | A | 2 | a0001c0002t0010g0213a0001c0002t0010g0264 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1279-1150G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21239394 | ||||||
chr1:21239557 | T | C | 2 | a0001c0002t0011g0016a0001c0002t0011g0241 | 2 | HG02895.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1279-1313A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21239557 | ||||||
chr1:21239604 | C | A | 1 | a0001c0003t0002g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1279-1360G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21239604 | ||||||
chr1:21239632 | T | A | 1 | a0001c0002t0005g0243 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1279-1388A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21239632 | ||||||
chr1:21239671 | C | T | 3 | a0001c0002t0012g0108a0001c0002t0012g0234a0001c0017t0020g0235 | 3 | HG01884.hp2 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1279-1427G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21239671 | ||||||
chr1:21239695 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1279-1451A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21239695 | ||||||
chr1:21239731 | G | A | 2 | a0001c0001t0003g0288a0001c0003t0003g0099 | 2 | HG01106.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1279-1487C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21239731 | ||||||
chr1:21239772 | C | T | 1 | a0009c0009t0002g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1279-1528G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21239772 | ||||||
chr1:21239957 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1279-1713C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21239957 | ||||||
chr1:21240032 | G | A | 8 | a0001c0001t0002g0254a0001c0001t0002g0255a0001c0001t0002g0272others(5): Show | 8 | HG01243.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279-1788C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21240032 | ||||||
chr1:21240349 | T | C | 19 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0251others(16): Show | 19 | HG01069.hp1 HG01106.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1279-2105A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21240349 | ||||||
chr1:21240360 | A | C | 2 | a0002c0006t0015g0011a0002c0006t0016g0172 | 2 | HG01074.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1279-2116T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21240360 | ||||||
chr1:21240588 | CAAGA | C | 46 | a0001c0001t0001g0072a0001c0001t0001g0089a0001c0001t0001g0092others(43): Show | 48 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1279-2348_1279-234 others(8): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21240588 | ||||||
chr1:21240692 | C | T | 46 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0251others(43): Show | 47 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.1279-2448G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21240692 | ||||||
chr1:21240778 | G | A | 2 | a0001c0002t0004g0265a0001c0002t0004g0266 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1279-2534C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21240778 | ||||||
chr1:21241002 | C | T | 21 | a0001c0002t0004g0009a0001c0002t0004g0084a0001c0002t0004g0098others(18): Show | 22 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1279-2758G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241002 | ||||||
chr1:21241063 | C | T | 2 | a0001c0001t0003g0288a0001c0003t0003g0099 | 2 | HG01106.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1279-2819G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241063 | ||||||
chr1:21241091 | G | A | 2 | a0001c0001t0003g0288a0001c0003t0003g0099 | 2 | HG01106.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1279-2847C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241091 | ||||||
chr1:21241199 | G | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(22): Show | 27 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.1279-2955C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241199 | ||||||
chr1:21241233 | G | A | 2 | a0002c0006t0015g0011a0002c0006t0016g0172 | 2 | HG01074.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1279-2989C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241233 | ||||||
chr1:21241283 | G | A | 2 | a0001c0002t0005g0201a0001c0002t0005g0205 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1279-3039C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241283 | ||||||
chr1:21241412 | G | A | 1 | a0001c0001t0003g0047 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1279-3168C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241412 | ||||||
chr1:21241423 | G | GT | 77 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0053others(74): Show | 80 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.1279-3180dupA | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241423 | ||||||
chr1:21241423 | G | GTT | 6 | a0001c0001t0001g0238a0001c0002t0005g0237a0001c0002t0005g0242others(3): Show | 6 | HG01243.hp2 HG02109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279-3181_1279-318 others(6): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241423 | ||||||
chr1:21241459 | G | A | 4 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(1): Show | 5 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-3215C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241459 | ||||||
chr1:21241581 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1279-3337G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241581 | ||||||
chr1:21241665 | C | T | 1 | a0001c0003t0002g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1278+3324G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241665 | ||||||
chr1:21241782 | C | T | 2 | a0001c0001t0003g0288a0001c0003t0003g0099 | 2 | HG01106.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1278+3207G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241782 | ||||||
chr1:21241829 | T | C | 3 | a0001c0001t0002g0262a0001c0001t0002g0286a0001c0001t0002g0290 | 3 | HG01099.hp1 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1278+3160A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241829 | ||||||
chr1:21241872 | G | A | 1 | a0010c0018t0017g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1278+3117C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21241872 | ||||||
chr1:21242077 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1278+2912C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21242077 | ||||||
chr1:21242089 | G | A | 2 | a0001c0001t0003g0288a0001c0003t0003g0099 | 2 | HG01106.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1278+2900C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21242089 | ||||||
chr1:21242215 | G | A | 2 | a0001c0002t0005g0201a0001c0002t0005g0205 | 2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1278+2774C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21242215 | ||||||
chr1:21242437 | T | G | 2 | a0002c0006t0015g0011a0002c0006t0016g0172 | 2 | HG01074.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1278+2552A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21242437 | ||||||
chr1:21242855 | G | A | 1 | a0001c0003t0002g0021 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1278+2134C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21242855 | ||||||
chr1:21242860 | A | G | 68 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(65): Show | 71 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1278+2129T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21242860 | ||||||
chr1:21242937 | C | T | 3 | a0001c0002t0012g0108a0001c0002t0012g0234a0001c0017t0020g0235 | 3 | HG01884.hp2 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1278+2052G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21242937 | ||||||
chr1:21243098 | A | G | 1 | a0001c0002t0005g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1278+1891T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21243098 | ||||||
chr1:21243188 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1278+1801T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21243188 | ||||||
chr1:21243223 | G | A | 1 | a0001c0001t0003g0028 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1278+1766C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21243223 | ||||||
chr1:21243400 | TA | T | 27 | a0001c0001t0001g0058a0001c0001t0001g0064a0001c0001t0001g0238others(24): Show | 27 | HG01069.hp1 HG01109.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1278+1588delT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21243400 | ||||||
chr1:21243400 | TAA | T | 25 | a0001c0001t0002g0255a0001c0001t0002g0271a0001c0001t0002g0277others(22): Show | 26 | HG00639.hp2 HG01106.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1278+1587_1278+158 others(6): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21243400 | ||||||
chr1:21243400 | TAAA | T | 76 | a0001c0001t0002g0067a0001c0001t0002g0109a0001c0001t0002g0114others(73): Show | 79 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.1278+1586_1278+158 others(7): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21243400 | ||||||
chr1:21243518 | C | T | 1 | a0001c0001t0013g0179 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1278+1471G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21243518 | ||||||
chr1:21243618 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1278+1371A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21243618 | ||||||
chr1:21243654 | C | G | 4 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(1): Show | 5 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1278+1335G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21243654 | ||||||
chr1:21243916 | T | C | 4 | a0001c0001t0008g0204a0001c0001t0008g0247a0001c0001t0008g0248others(1): Show | 4 | NA18947.hp2 NA18954.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+1073A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21243916 | ||||||
chr1:21243933 | C | T | 25 | a0001c0001t0001g0191a0001c0001t0001g0238a0001c0001t0001g0240others(22): Show | 25 | HG01069.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1278+1056G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21243933 | ||||||
chr1:21243992 | C | T | 1 | a0001c0002t0011g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1278+997G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21243992 | ||||||
chr1:21244012 | C | T | 2 | a0001c0001t0035g0097a0001c0002t0004g0098 | 2 | HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1278+977G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21244012 | ||||||
chr1:21244128 | T | C | 1 | a0001c0003t0002g0050 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1278+861A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21244128 | ||||||
chr1:21244190 | T | C | 5 | a0002c0004t0006g0002a0002c0004t0006g0010a0002c0004t0006g0013others(2): Show | 6 | HG00140.hp1 HG01074.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1278+799A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21244190 | ||||||
chr1:21244300 | G | A | 1 | a0001c0001t0003g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1278+689C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21244300 | ||||||
chr1:21244366 | G | C | 2 | a0001c0001t0035g0097a0001c0002t0004g0098 | 2 | HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1278+623C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21244366 | ||||||
chr1:21244638 | G | A | 25 | a0001c0001t0001g0191a0001c0001t0001g0238a0001c0001t0001g0240others(22): Show | 25 | HG01069.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1278+351C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21244638 | ||||||
chr1:21244982 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG04115.hp1 | splice_region_variant&intron_variant | LOW | c.1278+7C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 10/18 | chr1 | 21244982 | ||||||
chr1:21245108 | G | A | 43 | a0001c0001t0002g0114a0001c0001t0002g0123a0001c0001t0002g0165others(40): Show | 44 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(41): Show |
splice_region_variant&intron_variant | LOW | c.1164-5C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21245108 | ||||||
chr1:21245152 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1164-49C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21245152 | ||||||
chr1:21245170 | G | C | 1 | a0001c0001t0001g0025 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1164-67C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21245170 | ||||||
chr1:21245399 | GC | G | 27 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(24): Show | 27 | HG00639.hp2 HG01099.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1164-297delG | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21245399 | ||||||
chr1:21245623 | C | T | 1 | a0001c0002t0005g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1164-520G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21245623 | ||||||
chr1:21245689 | C | A | 7 | a0001c0001t0003g0004a0001c0001t0003g0028a0001c0001t0003g0029others(4): Show | 8 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.1164-586G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21245689 | ||||||
chr1:21245715 | G | T | 13 | a0001c0001t0001g0053a0001c0001t0001g0089a0001c0001t0001g0092others(10): Show | 13 | HG02155.hp2 HG02257.hp2 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1164-612C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21245715 | ||||||
chr1:21245914 | A | T | 5 | a0002c0004t0006g0002a0002c0004t0006g0010a0002c0004t0006g0013others(2): Show | 6 | HG00140.hp1 HG01074.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1164-811T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21245914 | ||||||
chr1:21246016 | G | C | 7 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(4): Show | 8 | HG01167.hp2 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1164-913C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246016 | ||||||
chr1:21246082 | T | C | 19 | a0001c0001t0001g0191a0001c0001t0002g0272a0001c0001t0003g0018others(16): Show | 19 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1164-979A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246082 | ||||||
chr1:21246109 | T | A | 27 | a0001c0001t0001g0191a0001c0001t0001g0238a0001c0001t0001g0240others(24): Show | 27 | HG01069.hp1 HG01109.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1164-1006A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246109 | ||||||
chr1:21246110 | T | A | 8 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0251others(5): Show | 8 | HG01069.hp1 HG01109.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.1164-1007A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246110 | ||||||
chr1:21246135 | G | C | 1 | a0001c0002t0004g0265 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1164-1032C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246135 | ||||||
chr1:21246197 | T | A | 3 | a0001c0001t0002g0255a0001c0001t0002g0271a0001c0001t0002g0277 | 3 | HG00639.hp2 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1163+1024A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246197 | ||||||
chr1:21246303 | C | T | 3 | a0001c0002t0012g0108a0001c0002t0012g0234a0001c0017t0020g0235 | 3 | HG01884.hp2 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1163+918G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246303 | ||||||
chr1:21246356 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1163+865G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246356 | ||||||
chr1:21246391 | T | C | 1 | a0001c0001t0003g0068 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1163+830A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246391 | ||||||
chr1:21246404 | C | T | 43 | a0001c0001t0002g0114a0001c0001t0002g0123a0001c0001t0002g0165others(40): Show | 44 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1163+817G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246404 | ||||||
chr1:21246455 | C | T | 1 | a0001c0002t0005g0243 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1163+766G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246455 | ||||||
chr1:21246498 | C | CA | 69 | a0001c0001t0001g0020a0001c0001t0001g0045a0001c0001t0001g0059others(66): Show | 71 | HG00140.hp2 HG00558.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1163+722dupT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246498 | ||||||
chr1:21246498 | C | CAA | 31 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0027others(28): Show | 33 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1163+721_1163+722d others(4): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246498 | ||||||
chr1:21246498 | CA | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(58): Show | 64 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1163+722delT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246498 | ||||||
chr1:21246514 | AG | A | 7 | a0001c0001t0003g0258a0001c0001t0007g0008a0001c0001t0007g0246others(4): Show | 8 | HG01069.hp1 HG01167.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1163+706delC | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246514 | ||||||
chr1:21246515 | G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(78): Show | 84 | HG00323.hp2 HG00558.hp2 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.1163+706C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246515 | ||||||
chr1:21246582 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1163+639T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246582 | ||||||
chr1:21246614 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1163+607A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246614 | ||||||
chr1:21246806 | C | T | 7 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(4): Show | 8 | HG01167.hp2 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1163+415G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246806 | ||||||
chr1:21246851 | G | A | 2 | a0001c0001t0001g0251a0001c0002t0004g0084 | 2 | HG01109.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1163+370C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246851 | ||||||
chr1:21246878 | C | G | 49 | a0001c0001t0002g0114a0001c0001t0002g0123a0001c0001t0002g0165others(46): Show | 51 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.1163+343G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21246878 | ||||||
chr1:21247012 | C | T | 1 | a0001c0001t0003g0160 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1163+209G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21247012 | ||||||
chr1:21247075 | G | A | 1 | a0001c0001t0003g0162 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1163+146C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21247075 | ||||||
chr1:21247107 | G | C | 5 | a0002c0004t0006g0002a0002c0004t0006g0010a0002c0004t0006g0013others(2): Show | 6 | HG00140.hp1 HG01074.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1163+114C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21247107 | ||||||
chr1:21247110 | C | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(83): Show | 90 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.1163+111G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21247110 | ||||||
chr1:21247212 | T | G | 1 | a0001c0003t0002g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1163+9A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 9/18 | chr1 | 21247212 | ||||||
chr1:21247388 | C | T | 10 | a0001c0001t0002g0109a0001c0001t0002g0190a0001c0001t0002g0255others(7): Show | 10 | HG00639.hp2 HG01099.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1021-25G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21247388 | ||||||
chr1:21247503 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1021-140G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21247503 | ||||||
chr1:21247514 | G | A | 1 | a0001c0003t0001g0145 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1021-151C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21247514 | ||||||
chr1:21247694 | C | T | 7 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(4): Show | 8 | HG01167.hp2 HG02622.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021-331G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21247694 | ||||||
chr1:21247801 | T | G | 1 | a0001c0002t0011g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1021-438A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21247801 | ||||||
chr1:21247894 | G | C | 2 | a0001c0002t0005g0104a0001c0007t0004g0215 | 2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1021-531C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21247894 | ||||||
chr1:21248022 | T | C | 7 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0251others(4): Show | 7 | HG01069.hp1 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1021-659A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248022 | ||||||
chr1:21248093 | G | C | 2 | a0001c0001t0003g0163a0001c0001t0003g0177 | 2 | NA18951.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1021-730C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248093 | ||||||
chr1:21248205 | C | G | 2 | a0001c0001t0002g0254a0001c0002t0004g0281 | 2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1021-842G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248205 | ||||||
chr1:21248308 | T | A | 1 | a0001c0002t0014g0230 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1021-945A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248308 | ||||||
chr1:21248345 | C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(65): Show | 71 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.1021-982G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248345 | ||||||
chr1:21248429 | C | A | 1 | a0001c0003t0002g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1021-1066G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248429 | ||||||
chr1:21248552 | A | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(113): Show | 121 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1021-1189T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248552 | ||||||
chr1:21248659 | C | T | 1 | a0009c0009t0002g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1021-1296G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248659 | ||||||
chr1:21248727 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1021-1364G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248727 | ||||||
chr1:21248745 | C | A | 1 | a0006c0011t0003g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1021-1382G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248745 | ||||||
chr1:21248750 | T | G | 1 | a0006c0011t0003g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1021-1387A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248750 | ||||||
chr1:21248762 | T | C | 1 | a0006c0011t0003g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1021-1399A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248762 | ||||||
chr1:21248769 | T | C | 1 | a0006c0011t0003g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1021-1406A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248769 | ||||||
chr1:21248770 | G | A | 1 | a0006c0011t0003g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1021-1407C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248770 | ||||||
chr1:21248773 | A | T | 1 | a0006c0011t0003g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1021-1410T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248773 | ||||||
chr1:21248774 | G | A | 1 | a0006c0011t0003g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1021-1411C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248774 | ||||||
chr1:21248782 | T | G | 1 | a0006c0011t0003g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1021-1419A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248782 | ||||||
chr1:21248785 | T | C | 1 | a0006c0011t0003g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1021-1422A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248785 | ||||||
chr1:21248786 | G | A | 1 | a0006c0011t0003g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1021-1423C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248786 | ||||||
chr1:21248963 | C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(65): Show | 71 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.1021-1600G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248963 | ||||||
chr1:21248995 | C | T | 5 | a0001c0002t0009g0239a0001c0002t0010g0213a0001c0002t0010g0264others(2): Show | 5 | HG02280.hp2 HG02818.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1021-1632G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21248995 | ||||||
chr1:21249054 | T | C | 1 | a0001c0002t0011g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1021-1691A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249054 | ||||||
chr1:21249071 | C | T | 107 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(104): Show | 111 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1021-1708G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249071 | ||||||
chr1:21249329 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1021-1966G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249329 | ||||||
chr1:21249340 | C | G | 18 | a0001c0001t0002g0109a0001c0001t0002g0190a0001c0001t0002g0254others(15): Show | 18 | HG00639.hp2 HG01099.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1021-1977G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249340 | ||||||
chr1:21249465 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1021-2102C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249465 | ||||||
chr1:21249490 | G | C | 7 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0251others(4): Show | 7 | HG01069.hp1 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1021-2127C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249490 | ||||||
chr1:21249532 | CA | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(130): Show | 138 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1021-2170delT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249532 | ||||||
chr1:21249611 | G | A | 18 | a0001c0001t0002g0109a0001c0001t0002g0190a0001c0001t0002g0254others(15): Show | 18 | HG00639.hp2 HG01099.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1021-2248C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249611 | ||||||
chr1:21249614 | C | T | 4 | a0001c0001t0002g0282a0001c0001t0035g0097a0001c0002t0004g0084others(1): Show | 4 | HG01109.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021-2251G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249614 | ||||||
chr1:21249704 | G | A | 1 | a0001c0002t0011g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1021-2341C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249704 | ||||||
chr1:21249780 | T | G | 4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG02717.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021-2417A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249780 | ||||||
chr1:21249867 | G | A | 1 | a0003c0016t0023g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1021-2504C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249867 | ||||||
chr1:21249939 | A | ATT | 10 | a0001c0001t0001g0251a0001c0001t0001g0269a0001c0002t0005g0237others(7): Show | 11 | HG00140.hp1 HG01069.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1021-2578_1021-257 others(6): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249939 | ||||||
chr1:21249939 | A | ATTTT | 35 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(32): Show | 37 | HG00323.hp2 HG00558.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1021-2580_1021-257 others(8): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249939 | ||||||
chr1:21249939 | A | ATTTTT | 15 | a0001c0001t0001g0031a0001c0001t0001g0035a0001c0001t0002g0272others(12): Show | 15 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1021-2581_1021-257 others(9): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249939 | ||||||
chr1:21249939 | AT | A | 24 | a0001c0001t0001g0095a0001c0001t0001g0124a0001c0001t0001g0153others(21): Show | 24 | HG00639.hp2 HG01099.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.1021-2577delA | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21249939 | ||||||
chr1:21250211 | A | G | 1 | a0001c0003t0003g0099 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1021-2848T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250211 | ||||||
chr1:21250228 | G | T | 2 | a0001c0002t0005g0231a0001c0002t0005g0232 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1021-2865C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250228 | ||||||
chr1:21250298 | T | G | 2 | a0001c0002t0014g0229a0001c0002t0014g0230 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1021-2935A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250298 | ||||||
chr1:21250303 | C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(35): Show | 40 | HG00323.hp2 HG00558.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.1021-2940G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250303 | ||||||
chr1:21250408 | C | T | 2 | a0003c0016t0023g0233a0009c0009t0002g0270 | 2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1021-3045G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250408 | ||||||
chr1:21250427 | G | T | 7 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0251others(4): Show | 7 | HG01069.hp1 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1021-3064C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250427 | ||||||
chr1:21250666 | T | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(223): Show | 235 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1021-3303A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250666 | ||||||
chr1:21250709 | C | T | 5 | a0002c0004t0006g0002a0002c0004t0006g0010a0002c0004t0006g0013others(2): Show | 6 | HG00140.hp1 HG01074.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021-3346G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250709 | ||||||
chr1:21250710 | G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(106): Show | 113 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1021-3347C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250710 | ||||||
chr1:21250730 | G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(49): Show | 54 | HG00323.hp2 HG00558.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.1021-3367C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250730 | ||||||
chr1:21250736 | G | A | 1 | a0001c0005t0001g0043 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1021-3373C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250736 | ||||||
chr1:21250863 | C | T | 60 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(57): Show | 63 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1021-3500G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250863 | ||||||
chr1:21250872 | T | C | 3 | a0001c0001t0001g0220a0001c0001t0001g0221a0005c0010t0001g0073 | 3 | HG00673.hp1 NA18612.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1021-3509A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250872 | ||||||
chr1:21250924 | A | G | 2 | a0003c0016t0023g0233a0009c0009t0002g0270 | 2 | HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1021-3561T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250924 | ||||||
chr1:21250931 | C | T | 2 | a0001c0001t0001g0095a0001c0007t0004g0215 | 2 | HG02723.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1021-3568G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250931 | ||||||
chr1:21250972 | AC | A | 42 | a0001c0001t0001g0143a0001c0001t0002g0114a0001c0001t0002g0165others(39): Show | 43 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1021-3610delG | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250972 | ||||||
chr1:21250985 | C | T | 18 | a0001c0001t0002g0109a0001c0001t0002g0190a0001c0001t0002g0254others(15): Show | 18 | HG00639.hp2 HG01099.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1021-3622G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21250985 | ||||||
chr1:21251002 | G | A | 3 | a0001c0002t0012g0108a0001c0002t0012g0234a0001c0017t0020g0235 | 3 | HG01884.hp2 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1021-3639C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21251002 | ||||||
chr1:21251006 | C | CA | 29 | a0001c0001t0001g0092a0001c0001t0001g0107a0001c0001t0001g0238others(26): Show | 29 | HG00639.hp2 HG01069.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.1021-3644dupT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21251006 | ||||||
chr1:21251006 | CA | C | 41 | a0001c0001t0001g0143a0001c0001t0002g0114a0001c0001t0002g0165others(38): Show | 42 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1021-3644delT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21251006 | ||||||
chr1:21251117 | G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(48): Show | 54 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1021-3754C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21251117 | ||||||
chr1:21251395 | A | G | 27 | a0001c0001t0002g0109a0001c0001t0002g0190a0001c0001t0002g0254others(24): Show | 28 | HG00639.hp2 HG01099.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1021-4032T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21251395 | ||||||
chr1:21251423 | G | T | 1 | a0006c0011t0003g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1021-4060C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21251423 | ||||||
chr1:21251501 | C | T | 1 | a0009c0009t0002g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1021-4138G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21251501 | ||||||
chr1:21251602 | G | A | 18 | a0001c0001t0002g0109a0001c0001t0002g0190a0001c0001t0002g0254others(15): Show | 18 | HG00639.hp2 HG01099.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1021-4239C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21251602 | ||||||
chr1:21251621 | C | A | 3 | a0001c0002t0012g0108a0001c0002t0012g0234a0001c0017t0020g0235 | 3 | HG01884.hp2 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1021-4258G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21251621 | ||||||
chr1:21251729 | G | C | 5 | a0002c0004t0006g0002a0002c0004t0006g0010a0002c0004t0006g0013others(2): Show | 6 | HG00140.hp1 HG01074.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1020+4218C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21251729 | ||||||
chr1:21252258 | G | C | 1 | a0001c0002t0009g0239 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1020+3689C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21252258 | ||||||
chr1:21252335 | A | C | 1 | a0001c0001t0001g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1020+3612T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21252335 | ||||||
chr1:21252364 | C | T | 1 | a0001c0003t0001g0197 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1020+3583G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21252364 | ||||||
chr1:21252633 | T | G | 1 | a0005c0010t0001g0073 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1020+3314A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21252633 | ||||||
chr1:21252751 | A | C | 1 | a0001c0003t0003g0099 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1020+3196T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21252751 | ||||||
chr1:21252841 | G | A | 14 | a0001c0001t0001g0191a0001c0001t0002g0272a0001c0001t0003g0018others(11): Show | 14 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1020+3106C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21252841 | ||||||
chr1:21253034 | ATTATT | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(181): Show | 191 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1020+2908_1020+291 others(9): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253034 | ||||||
chr1:21253034 | ATTATTTT others(8): Show |
A | 3 | a0001c0002t0012g0108a0001c0002t0012g0234a0001c0017t0020g0235 | 3 | HG01884.hp2 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1020+2898_1020+291 others(19): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253034 | ||||||
chr1:21253079 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1020+2868G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253079 | ||||||
chr1:21253119 | T | C | 1 | a0001c0001t0019g0192 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1020+2828A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253119 | ||||||
chr1:21253308 | C | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(84): Show | 91 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1020+2639G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253308 | ||||||
chr1:21253402 | T | A | 1 | a0001c0002t0009g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1020+2545A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253402 | ||||||
chr1:21253488 | C | A | 1 | a0001c0001t0003g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1020+2459G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253488 | ||||||
chr1:21253500 | C | T | 4 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(1): Show | 5 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+2447G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253500 | ||||||
chr1:21253501 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1020+2446C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253501 | ||||||
chr1:21253528 | C | T | 5 | a0002c0004t0006g0002a0002c0004t0006g0010a0002c0004t0006g0013others(2): Show | 6 | HG00140.hp1 HG01074.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1020+2419G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253528 | ||||||
chr1:21253534 | G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(84): Show | 90 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.1020+2413C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253534 | ||||||
chr1:21253566 | T | G | 1 | a0001c0001t0026g0134 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1020+2381A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253566 | ||||||
chr1:21253656 | G | C | 4 | a0001c0001t0002g0282a0001c0001t0035g0097a0001c0002t0004g0084others(1): Show | 4 | HG01109.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1020+2291C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253656 | ||||||
chr1:21253659 | A | G | 41 | a0001c0001t0001g0143a0001c0001t0002g0114a0001c0001t0002g0165others(38): Show | 42 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1020+2288T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253659 | ||||||
chr1:21253741 | C | T | 1 | a0001c0003t0002g0164 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1020+2206G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253741 | ||||||
chr1:21253767 | T | TA | 90 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(87): Show | 94 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1020+2179dupT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253767 | ||||||
chr1:21253778 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1020+2169T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253778 | ||||||
chr1:21253852 | T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(220): Show | 232 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.1020+2095A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253852 | ||||||
chr1:21253866 | C | T | 1 | a0001c0008t0002g0194 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1020+2081G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253866 | ||||||
chr1:21253867 | G | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(81): Show | 88 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1020+2080C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253867 | ||||||
chr1:21253906 | T | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(58): Show | 64 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1020+2041A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253906 | ||||||
chr1:21253926 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1020+2021C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21253926 | ||||||
chr1:21254068 | CA | C | 11 | a0001c0001t0001g0072a0001c0001t0001g0107a0001c0001t0001g0116others(8): Show | 11 | HG01167.hp1 HG01256.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1020+1878delT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21254068 | ||||||
chr1:21254068 | CAA | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(108): Show | 115 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.1020+1877_1020+187 others(6): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21254068 | ||||||
chr1:21254068 | CAAA | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(61): Show | 67 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.1020+1876_1020+187 others(7): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21254068 | ||||||
chr1:21254068 | CAAAA | C | 6 | a0001c0003t0002g0046a0001c0003t0002g0080a0001c0003t0002g0082others(3): Show | 6 | HG00140.hp2 HG00558.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1020+1875_1020+187 others(8): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21254068 | ||||||
chr1:21254068 | CAAAAA | C | 35 | a0001c0001t0001g0143a0001c0001t0002g0114a0001c0001t0002g0165others(32): Show | 36 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1020+1874_1020+187 others(9): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21254068 | ||||||
chr1:21254068 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0090 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1020+1868_1020+187 others(15): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21254068 | ||||||
chr1:21254262 | A | G | 18 | a0001c0001t0002g0109a0001c0001t0002g0190a0001c0001t0002g0254others(15): Show | 18 | HG00639.hp2 HG01099.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1020+1685T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21254262 | ||||||
chr1:21254407 | G | A | 1 | a0001c0001t0002g0165 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1020+1540C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21254407 | ||||||
chr1:21254528 | C | T | 43 | a0001c0001t0001g0143a0001c0001t0002g0114a0001c0001t0002g0165others(40): Show | 44 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1020+1419G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21254528 | ||||||
chr1:21254627 | C | T | 1 | a0003c0016t0023g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1020+1320G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21254627 | ||||||
chr1:21254722 | GAA | G | 61 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(58): Show | 64 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1020+1223_1020+122 others(6): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21254722 | ||||||
chr1:21254769 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1020+1178A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21254769 | ||||||
chr1:21255121 | C | A | 47 | a0001c0001t0001g0143a0001c0001t0002g0114a0001c0001t0002g0165others(44): Show | 49 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1020+826G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21255121 | ||||||
chr1:21255151 | G | T | 1 | a0001c0001t0001g0034 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1020+796C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21255151 | ||||||
chr1:21255272 | C | T | 85 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(82): Show | 89 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1020+675G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21255272 | ||||||
chr1:21255367 | C | T | 1 | a0001c0002t0004g0263 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1020+580G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21255367 | ||||||
chr1:21255392 | C | T | 1 | a0001c0002t0005g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1020+555G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21255392 | ||||||
chr1:21255486 | C | A | 48 | a0001c0001t0001g0143a0001c0001t0002g0114a0001c0001t0002g0165others(45): Show | 50 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.1020+461G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21255486 | ||||||
chr1:21255827 | C | T | 1 | a0001c0002t0010g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1020+120G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21255827 | ||||||
chr1:21255855 | T | C | 43 | a0001c0001t0001g0143a0001c0001t0002g0114a0001c0001t0002g0165others(40): Show | 44 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1020+92A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21255855 | ||||||
chr1:21255893 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1020+54A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21255893 | ||||||
chr1:21255932 | C | T | 38 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(35): Show | 40 | HG00323.hp2 HG00558.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.1020+15G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 8/18 | chr1 | 21255932 | ||||||
chr1:21256226 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.829-88G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256226 | ||||||
chr1:21256328 | G | T | 48 | a0001c0001t0001g0143a0001c0001t0002g0114a0001c0001t0002g0165others(45): Show | 50 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.829-190C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256328 | ||||||
chr1:21256377 | G | A | 1 | a0001c0002t0004g0285 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.829-239C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256377 | ||||||
chr1:21256381 | C | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(59): Show | 64 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.829-243G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256381 | ||||||
chr1:21256438 | C | T | 1 | a0009c0009t0002g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.829-300G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256438 | ||||||
chr1:21256510 | T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(223): Show | 235 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.829-372A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256510 | ||||||
chr1:21256511 | G | A | 1 | a0009c0009t0002g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.829-373C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256511 | ||||||
chr1:21256512 | T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(35): Show | 40 | HG00323.hp2 HG00558.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.829-374A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256512 | ||||||
chr1:21256615 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.829-477G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256615 | ||||||
chr1:21256670 | C | T | 7 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0251others(4): Show | 7 | HG01069.hp1 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.829-532G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256670 | ||||||
chr1:21256767 | C | A | 2 | a0001c0001t0003g0125a0001c0001t0007g0245 | 2 | HG02976.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.829-629G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256767 | ||||||
chr1:21256818 | T | C | 230 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(227): Show | 239 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.829-680A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256818 | ||||||
chr1:21256820 | A | T | 4 | a0001c0001t0001g0143a0001c0003t0001g0145a0001c0003t0001g0188others(1): Show | 4 | HG01255.hp1 HG02258.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.829-682T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256820 | ||||||
chr1:21256852 | C | T | 5 | a0002c0004t0006g0002a0002c0004t0006g0010a0002c0004t0006g0013others(2): Show | 6 | HG00140.hp1 HG01074.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.828+673G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256852 | ||||||
chr1:21256895 | T | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG01070.hp1 HG01071.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.828+630A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256895 | ||||||
chr1:21256998 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.828+527C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21256998 | ||||||
chr1:21257242 | T | C | 4 | a0001c0001t0002g0282a0001c0001t0035g0097a0001c0002t0004g0084others(1): Show | 4 | HG01109.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.828+283A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21257242 | ||||||
chr1:21257339 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.828+186A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21257339 | ||||||
chr1:21257373 | C | T | 16 | a0001c0001t0001g0191a0001c0001t0002g0272a0001c0001t0003g0018others(13): Show | 16 | HG01069.hp2 HG01071.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.828+152G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21257373 | ||||||
chr1:21257432 | C | T | 43 | a0001c0001t0001g0143a0001c0001t0002g0114a0001c0001t0002g0165others(40): Show | 44 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.828+93G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21257432 | ||||||
chr1:21257461 | G | T | 1 | a0001c0001t0028g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.828+64C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21257461 | ||||||
chr1:21257480 | A | G | 43 | a0001c0001t0001g0143a0001c0001t0002g0114a0001c0001t0002g0165others(40): Show | 44 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.828+45T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21257480 | ||||||
chr1:21257485 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.828+40G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21257485 | ||||||
chr1:21257517 | A | G | 7 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0251others(4): Show | 7 | HG01069.hp1 HG01243.hp2 HG02109.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.828+8T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 7/18 | chr1 | 21257517 | ||||||
chr1:21257665 | G | A | 1 | a0009c0009t0002g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.763-75C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 6/18 | chr1 | 21257665 | ||||||
chr1:21257755 | C | T | 1 | a0001c0003t0003g0099 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.763-165G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 6/18 | chr1 | 21257755 | ||||||
chr1:21257785 | G | GC | 42 | a0001c0001t0001g0006a0001c0001t0001g0143a0001c0001t0001g0187others(39): Show | 44 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.763-196dupG | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 6/18 | chr1 | 21257785 | ||||||
chr1:21257794 | C | CG | 4 | a0001c0003t0002g0080a0001c0003t0002g0082a0001c0003t0002g0083others(1): Show | 4 | HG00140.hp2 HG00558.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.763-205dupC | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 6/18 | chr1 | 21257794 | ||||||
chr1:21257794 | C | G | 1 | a0001c0003t0002g0046 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.763-204G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 6/18 | chr1 | 21257794 | ||||||
chr1:21258092 | A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(232): Show | 244 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.763-502T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 6/18 | chr1 | 21258092 | ||||||
chr1:21258330 | G | A | 1 | a0001c0002t0004g0293 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.762+363C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 6/18 | chr1 | 21258330 | ||||||
chr1:21258352 | T | C | 5 | a0001c0001t0003g0288a0001c0002t0004g0256a0001c0002t0004g0267others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.762+341A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 6/18 | chr1 | 21258352 | ||||||
chr1:21258448 | T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(232): Show | 245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.762+245A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 6/18 | chr1 | 21258448 | ||||||
chr1:21258521 | C | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(41): Show | 46 | HG00323.hp2 HG00558.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.762+172G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 6/18 | chr1 | 21258521 | ||||||
chr1:21258936 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.616-97C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/18 | chr1 | 21258936 | ||||||
chr1:21259087 | G | A | 1 | a0001c0001t0003g0007 | 2 | HG02004.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.616-248C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/18 | chr1 | 21259087 | ||||||
chr1:21259122 | G | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0110a0001c0001t0001g0111others(1): Show | 4 | HG01175.hp1 HG02055.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.616-283C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/18 | chr1 | 21259122 | ||||||
chr1:21259153 | G | A | 2 | a0001c0003t0001g0216a0001c0003t0001g0217 | 2 | NA18954.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.616-314C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/18 | chr1 | 21259153 | ||||||
chr1:21259168 | T | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(39): Show | 44 | HG00323.hp2 HG00558.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.616-329A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/18 | chr1 | 21259168 | ||||||
chr1:21259270 | T | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(64): Show | 69 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.616-431A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/18 | chr1 | 21259270 | ||||||
chr1:21259278 | T | A | 2 | a0001c0001t0001g0118a0001c0001t0027g0115 | 2 | HG01515.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.616-439A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/18 | chr1 | 21259278 | ||||||
chr1:21259305 | A | C | 1 | a0001c0001t0002g0287 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.616-466T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/18 | chr1 | 21259305 | ||||||
chr1:21259411 | G | A | 1 | a0001c0002t0009g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.616-572C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/18 | chr1 | 21259411 | ||||||
chr1:21259418 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.616-579A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/18 | chr1 | 21259418 | ||||||
chr1:21259637 | T | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(34): Show | 39 | HG00323.hp2 HG00558.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.615+634A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/18 | chr1 | 21259637 | ||||||
chr1:21259973 | C | T | 4 | a0001c0001t0003g0288a0001c0002t0004g0256a0001c0002t0004g0285others(1): Show | 4 | HG02145.hp2 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.615+298G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/18 | chr1 | 21259973 | ||||||
chr1:21260109 | A | G | 3 | a0001c0001t0007g0273a0001c0001t0007g0275a0001c0001t0028g0294 | 3 | HG01167.hp2 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.615+162T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/18 | chr1 | 21260109 | ||||||
chr1:21260212 | CA | C | 4 | a0001c0001t0002g0282a0001c0001t0035g0097a0001c0002t0004g0084others(1): Show | 4 | HG01109.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.615+58delT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 5/18 | chr1 | 21260212 | ||||||
chr1:21260685 | C | T | 3 | a0001c0002t0012g0108a0001c0002t0012g0234a0001c0017t0020g0235 | 3 | HG01884.hp2 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.494-293G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21260685 | ||||||
chr1:21260879 | G | C | 1 | a0001c0002t0011g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.494-487C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21260879 | ||||||
chr1:21260952 | C | G | 86 | a0001c0001t0001g0006a0001c0001t0001g0136a0001c0001t0001g0143others(83): Show | 90 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.494-560G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21260952 | ||||||
chr1:21261030 | G | T | 1 | a0001c0001t0002g0142 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.494-638C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21261030 | ||||||
chr1:21261062 | A | C | 5 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(2): Show | 6 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.494-670T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21261062 | ||||||
chr1:21261356 | G | A | 86 | a0001c0001t0001g0006a0001c0001t0001g0136a0001c0001t0001g0143others(83): Show | 90 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.494-964C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21261356 | ||||||
chr1:21261623 | G | A | 85 | a0001c0001t0001g0006a0001c0001t0001g0136a0001c0001t0001g0143others(82): Show | 89 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.494-1231C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21261623 | ||||||
chr1:21261758 | C | A | 1 | a0002c0006t0016g0172 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.494-1366G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21261758 | ||||||
chr1:21261785 | G | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(39): Show | 44 | HG00323.hp2 HG00558.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.494-1393C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21261785 | ||||||
chr1:21261797 | C | T | 1 | a0001c0008t0002g0194 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.494-1405G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21261797 | ||||||
chr1:21261846 | G | A | 1 | a0001c0001t0002g0183 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.494-1454C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21261846 | ||||||
chr1:21262068 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.494-1676A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21262068 | ||||||
chr1:21262072 | T | C | 3 | a0001c0002t0012g0108a0001c0002t0012g0234a0001c0017t0020g0235 | 3 | HG01884.hp2 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.494-1680A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21262072 | ||||||
chr1:21262109 | C | G | 1 | a0001c0002t0004g0293 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.494-1717G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21262109 | ||||||
chr1:21262110 | C | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(237): Show | 250 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.494-1718G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21262110 | ||||||
chr1:21262379 | A | T | 1 | a0001c0017t0020g0235 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.494-1987T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21262379 | ||||||
chr1:21262555 | G | A | 1 | a0001c0003t0002g0051 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.494-2163C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21262555 | ||||||
chr1:21262608 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.494-2216G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21262608 | ||||||
chr1:21262990 | C | T | 3 | a0001c0001t0035g0097a0001c0002t0004g0084a0001c0002t0004g0098 | 3 | HG01109.hp2 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.494-2598G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21262990 | ||||||
chr1:21262992 | C | T | 1 | a0001c0001t0003g0102 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.494-2600G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21262992 | ||||||
chr1:21263013 | G | A | 3 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245 | 4 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-2621C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263013 | ||||||
chr1:21263163 | C | T | 1 | a0001c0002t0011g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.494-2771G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263163 | ||||||
chr1:21263164 | T | C | 1 | a0001c0002t0009g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.494-2772A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263164 | ||||||
chr1:21263173 | G | A | 90 | a0001c0001t0001g0006a0001c0001t0001g0136a0001c0001t0001g0143others(87): Show | 94 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.494-2781C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263173 | ||||||
chr1:21263184 | T | A | 1 | a0001c0002t0011g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.494-2792A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263184 | ||||||
chr1:21263250 | T | C | 2 | a0001c0001t0001g0269a0001c0013t0004g0268 | 2 | HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.494-2858A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263250 | ||||||
chr1:21263327 | G | A | 6 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0251others(3): Show | 6 | HG01069.hp1 HG01243.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.494-2935C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263327 | ||||||
chr1:21263354 | T | C | 3 | a0001c0002t0011g0241a0003c0016t0023g0233a0009c0009t0002g0270 | 3 | HG03139.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.494-2962A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263354 | ||||||
chr1:21263361 | A | AT | 55 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(52): Show | 57 | HG00323.hp2 HG00558.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.494-2970dupA | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263361 | ||||||
chr1:21263361 | A | ATT | 7 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0251others(4): Show | 7 | HG01069.hp1 HG01106.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-2971_494-2970d others(4): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263361 | ||||||
chr1:21263361 | A | T | 71 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(68): Show | 73 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.494-2969T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263361 | ||||||
chr1:21263363 | T | TTA | 85 | a0001c0001t0001g0006a0001c0001t0001g0136a0001c0001t0001g0143others(82): Show | 89 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.494-2972_494-2971i others(4): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263363 | ||||||
chr1:21263388 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.494-2996G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263388 | ||||||
chr1:21263618 | T | C | 1 | a0001c0003t0003g0099 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.494-3226A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263618 | ||||||
chr1:21263636 | G | A | 14 | a0001c0001t0001g0269a0001c0001t0002g0261a0001c0001t0002g0286others(11): Show | 15 | HG01099.hp1 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.494-3244C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263636 | ||||||
chr1:21263662 | CT | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(225): Show | 237 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.494-3271delA | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263662 | ||||||
chr1:21263768 | C | T | 3 | a0001c0001t0007g0273a0001c0001t0007g0275a0001c0001t0028g0294 | 3 | HG01167.hp2 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.494-3376G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263768 | ||||||
chr1:21263828 | C | T | 1 | a0001c0002t0012g0108 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.494-3436G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263828 | ||||||
chr1:21263849 | G | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(68): Show | 73 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.494-3457C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263849 | ||||||
chr1:21263976 | G | A | 1 | a0001c0001t0002g0282 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.494-3584C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21263976 | ||||||
chr1:21264026 | G | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0026others(37): Show | 42 | HG00323.hp2 HG00558.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.494-3634C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264026 | ||||||
chr1:21264126 | G | A | 21 | a0001c0001t0001g0191a0001c0001t0002g0272a0001c0001t0003g0018others(18): Show | 22 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.494-3734C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264126 | ||||||
chr1:21264260 | C | T | 2 | a0001c0001t0003g0033a0001c0001t0003g0062 | 2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.494-3868G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264260 | ||||||
chr1:21264261 | A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 216 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.494-3869T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264261 | ||||||
chr1:21264274 | C | T | 1 | a0001c0001t0003g0125 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.494-3882G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264274 | ||||||
chr1:21264309 | T | TC | 21 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0096others(18): Show | 21 | HG00735.hp2 HG00738.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.494-3918dupG | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264309 | ||||||
chr1:21264312 | C | A | 1 | a0001c0002t0011g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.494-3920G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264312 | ||||||
chr1:21264313 | C | G | 1 | a0001c0002t0009g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.494-3921G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264313 | ||||||
chr1:21264317 | C | A | 4 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(1): Show | 5 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-3925G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264317 | ||||||
chr1:21264317 | C | CG | 3 | a0001c0001t0035g0097a0001c0002t0004g0084a0001c0002t0004g0098 | 3 | HG01109.hp2 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.494-3926_494-3925i others(3): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264317 | ||||||
chr1:21264318 | C | G | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 215 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.494-3926G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264318 | ||||||
chr1:21264319 | C | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0168 | 2 | HG02129.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.494-3927G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264319 | ||||||
chr1:21264319 | CCT | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(207): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.494-3929_494-3928d others(4): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264319 | ||||||
chr1:21264320 | C | T | 3 | a0001c0001t0035g0097a0001c0002t0004g0084a0001c0002t0004g0098 | 3 | HG01109.hp2 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.494-3928G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264320 | ||||||
chr1:21264321 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.494-3929A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264321 | ||||||
chr1:21264327 | T | G | 1 | a0001c0002t0005g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.494-3935A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264327 | ||||||
chr1:21264356 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.494-3964G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264356 | ||||||
chr1:21264380 | A | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 215 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.494-3988T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264380 | ||||||
chr1:21264551 | G | A | 14 | a0001c0001t0001g0191a0001c0001t0002g0272a0001c0001t0003g0018others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.494-4159C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264551 | ||||||
chr1:21264681 | G | A | 1 | a0001c0001t0003g0062 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.494-4289C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264681 | ||||||
chr1:21264840 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.494-4448G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21264840 | ||||||
chr1:21265157 | C | T | 1 | a0001c0003t0001g0145 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.494-4765G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21265157 | ||||||
chr1:21265387 | C | T | 12 | a0001c0001t0001g0191a0001c0001t0002g0272a0001c0001t0003g0018others(9): Show | 12 | HG01069.hp2 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.494-4995G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21265387 | ||||||
chr1:21265409 | G | A | 1 | a0001c0001t0003g0018 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.494-5017C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21265409 | ||||||
chr1:21265440 | A | G | 48 | a0001c0001t0001g0191a0001c0001t0001g0223a0001c0001t0001g0292others(45): Show | 49 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.494-5048T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21265440 | ||||||
chr1:21265486 | A | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(191): Show | 202 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.494-5094T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21265486 | ||||||
chr1:21265519 | G | A | 13 | a0001c0001t0001g0053a0001c0001t0001g0089a0001c0001t0001g0090others(10): Show | 13 | HG02257.hp2 HG02735.hp1 HG03130.hp1 others(10): Show |
intron_variant | MODIFIER | c.494-5127C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21265519 | ||||||
chr1:21265899 | A | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(236): Show | 249 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.494-5507T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21265899 | ||||||
chr1:21265978 | G | A | 1 | a0001c0002t0009g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.494-5586C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21265978 | ||||||
chr1:21266482 | G | A | 3 | a0001c0002t0014g0229a0001c0002t0014g0230a0001c0003t0003g0099 | 3 | HG01106.hp1 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.494-6090C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21266482 | ||||||
chr1:21266624 | C | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(235): Show | 248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.493+6075G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21266624 | ||||||
chr1:21266774 | G | A | 19 | a0001c0001t0001g0191a0001c0001t0001g0238a0001c0001t0001g0240others(16): Show | 19 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.493+5925C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21266774 | ||||||
chr1:21266937 | T | C | 5 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(2): Show | 6 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.493+5762A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21266937 | ||||||
chr1:21267210 | G | A | 35 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0001g0093others(32): Show | 35 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.493+5489C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21267210 | ||||||
chr1:21267280 | T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(217): Show | 229 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.493+5419A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21267280 | ||||||
chr1:21267292 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.493+5407A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21267292 | ||||||
chr1:21267447 | A | G | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0002c0004t0006g0010 | 3 | HG00323.hp2 HG02698.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.493+5252T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21267447 | ||||||
chr1:21267448 | G | C | 3 | a0001c0001t0006g0014a0001c0001t0006g0015a0002c0004t0006g0010 | 3 | HG00323.hp2 HG02698.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.493+5251C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21267448 | ||||||
chr1:21267475 | C | G | 2 | a0001c0003t0002g0021a0001c0003t0002g0022 | 2 | NA18994.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.493+5224G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21267475 | ||||||
chr1:21267509 | C | T | 9 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(6): Show | 10 | HG01109.hp2 HG02280.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.493+5190G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21267509 | ||||||
chr1:21267616 | G | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(108): Show | 117 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.493+5083C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21267616 | ||||||
chr1:21267774 | T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0170 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.493+4925A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21267774 | ||||||
chr1:21267817 | T | G | 1 | a0001c0001t0001g0094 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.493+4882A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21267817 | ||||||
chr1:21267907 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.493+4792G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21267907 | ||||||
chr1:21268115 | A | G | 3 | a0001c0002t0004g0084a0001c0002t0014g0229a0001c0002t0014g0230 | 3 | HG01109.hp2 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.493+4584T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21268115 | ||||||
chr1:21268169 | C | T | 8 | a0001c0001t0001g0212a0001c0001t0006g0012a0001c0001t0006g0014others(5): Show | 9 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.493+4530G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21268169 | ||||||
chr1:21268234 | T | C | 1 | a0003c0016t0023g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.493+4465A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21268234 | ||||||
chr1:21268329 | A | C | 1 | a0001c0001t0003g0062 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.493+4370T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21268329 | ||||||
chr1:21268361 | G | C | 1 | a0001c0001t0003g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.493+4338C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21268361 | ||||||
chr1:21268364 | GA | G | 4 | a0001c0002t0004g0084a0001c0002t0014g0229a0001c0002t0014g0230others(1): Show | 4 | HG01106.hp1 HG01109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+4334delT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21268364 | ||||||
chr1:21268469 | G | A | 4 | a0001c0002t0004g0084a0001c0002t0014g0229a0001c0002t0014g0230others(1): Show | 4 | HG01106.hp1 HG01109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+4230C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21268469 | ||||||
chr1:21268641 | C | T | 8 | a0001c0001t0001g0212a0001c0001t0006g0012a0001c0001t0006g0014others(5): Show | 9 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.493+4058G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21268641 | ||||||
chr1:21268688 | C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(70): Show | 77 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.493+4011G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21268688 | ||||||
chr1:21268763 | C | T | 1 | a0001c0002t0004g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.493+3936G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21268763 | ||||||
chr1:21268922 | C | T | 2 | a0001c0001t0001g0155a0001c0001t0003g0004 | 3 | NA18747.hp1 NA18975.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.493+3777G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21268922 | ||||||
chr1:21268965 | C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(70): Show | 77 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.493+3734G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21268965 | ||||||
chr1:21269060 | T | A | 36 | a0001c0001t0001g0292a0001c0001t0002g0228a0001c0001t0002g0254others(33): Show | 37 | HG00639.hp2 HG01099.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.493+3639A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21269060 | ||||||
chr1:21269062 | T | C | 1 | a0001c0001t0028g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.493+3637A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21269062 | ||||||
chr1:21269071 | C | T | 19 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(16): Show | 19 | HG01175.hp1 HG02257.hp2 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.493+3628G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21269071 | ||||||
chr1:21269118 | T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(160): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.493+3581A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21269118 | ||||||
chr1:21269168 | T | C | 1 | a0001c0002t0010g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.493+3531A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21269168 | ||||||
chr1:21269324 | T | C | 1 | a0009c0009t0002g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.493+3375A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21269324 | ||||||
chr1:21269798 | G | C | 1 | a0001c0002t0012g0108 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.493+2901C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21269798 | ||||||
chr1:21270303 | A | C | 36 | a0001c0001t0001g0292a0001c0001t0002g0228a0001c0001t0002g0254others(33): Show | 37 | HG00639.hp2 HG01099.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.493+2396T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21270303 | ||||||
chr1:21270324 | G | A | 5 | a0001c0001t0002g0228a0001c0001t0003g0288a0001c0002t0004g0256others(2): Show | 5 | HG02145.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+2375C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21270324 | ||||||
chr1:21270413 | T | C | 1 | a0001c0002t0011g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.493+2286A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21270413 | ||||||
chr1:21270852 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.493+1847G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21270852 | ||||||
chr1:21270920 | G | C | 1 | a0001c0001t0003g0154 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.493+1779C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21270920 | ||||||
chr1:21270921 | C | A | 1 | a0001c0001t0003g0154 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.493+1778G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21270921 | ||||||
chr1:21270953 | C | T | 1 | a0001c0002t0004g0084 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.493+1746G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21270953 | ||||||
chr1:21270982 | C | T | 1 | a0001c0001t0028g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.493+1717G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21270982 | ||||||
chr1:21270988 | A | G | 2 | a0001c0001t0035g0097a0001c0002t0004g0098 | 2 | HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.493+1711T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21270988 | ||||||
chr1:21271249 | C | T | 4 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(1): Show | 5 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+1450G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21271249 | ||||||
chr1:21271327 | T | A | 1 | a0001c0001t0003g0154 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.493+1372A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21271327 | ||||||
chr1:21271351 | G | A | 1 | a0001c0001t0002g0228 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.493+1348C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21271351 | ||||||
chr1:21271409 | A | G | 2 | a0001c0002t0005g0237a0001c0002t0005g0242 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.493+1290T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21271409 | ||||||
chr1:21271422 | T | G | 1 | a0001c0001t0001g0133 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.493+1277A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21271422 | ||||||
chr1:21271448 | T | G | 1 | a0001c0001t0031g0101 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.493+1251A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21271448 | ||||||
chr1:21271643 | C | T | 7 | a0001c0001t0006g0012a0001c0001t0006g0014a0001c0001t0006g0015others(4): Show | 8 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.493+1056G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21271643 | ||||||
chr1:21271667 | C | T | 1 | a0002c0006t0016g0172 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.493+1032G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21271667 | ||||||
chr1:21271741 | G | C | 1 | a0001c0001t0026g0134 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.493+958C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21271741 | ||||||
chr1:21271779 | G | T | 2 | a0001c0002t0004g0265a0001c0002t0004g0266 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.493+920C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21271779 | ||||||
chr1:21271841 | G | A | 2 | a0001c0001t0002g0228a0001c0002t0009g0227 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.493+858C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21271841 | ||||||
chr1:21271879 | G | A | 9 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0182others(6): Show | 9 | HG01081.hp2 HG02055.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.493+820C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21271879 | ||||||
chr1:21271884 | C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(69): Show | 76 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.493+815G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21271884 | ||||||
chr1:21271957 | T | C | 2 | a0001c0001t0002g0228a0001c0002t0009g0227 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.493+742A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21271957 | ||||||
chr1:21272440 | C | T | 3 | a0001c0001t0001g0251a0001c0002t0004g0249a0001c0002t0004g0250 | 3 | HG01069.hp2 HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.493+259G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 4/18 | chr1 | 21272440 | ||||||
chr1:21272973 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.281-62T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21272973 | ||||||
chr1:21273112 | C | G | 6 | a0001c0001t0003g0004a0001c0001t0003g0028a0001c0001t0003g0029others(3): Show | 7 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.281-201G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273112 | ||||||
chr1:21273151 | C | A | 1 | a0001c0001t0001g0090 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.281-240G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273151 | ||||||
chr1:21273306 | T | C | 19 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(16): Show | 19 | HG01175.hp1 HG02257.hp2 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.281-395A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273306 | ||||||
chr1:21273338 | CGTGTGTG others(7): Show |
C | 1 | a0001c0002t0011g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.281-441_281-428del others(14): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273338 | ||||||
chr1:21273338 | CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0031g0101 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.281-443_281-428del others(16): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273338 | ||||||
chr1:21273338 | CGTGTGTG others(11): Show |
C | 34 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0092others(31): Show | 34 | HG01081.hp2 HG01175.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.281-445_281-428del others(18): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273338 | ||||||
chr1:21273338 | CGTGTGTG others(13): Show |
C | 3 | a0001c0001t0001g0090a0001c0001t0035g0097a0001c0002t0004g0098 | 3 | HG03516.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.281-447_281-428del others(20): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273338 | ||||||
chr1:21273338 | CGTGTGTG others(19): Show |
C | 1 | a0001c0001t0001g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.281-453_281-428del others(26): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273338 | ||||||
chr1:21273346 | C | CGT | 69 | a0001c0001t0001g0119a0001c0001t0001g0124a0001c0001t0001g0136others(66): Show | 71 | HG00323.hp1 HG00408.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.281-437_281-436dup others(2): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273346 | ||||||
chr1:21273346 | C | CGTGT | 8 | a0001c0001t0002g0109a0001c0001t0003g0086a0001c0001t0013g0017others(5): Show | 8 | HG00735.hp1 HG01099.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-439_281-436dup others(4): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273346 | ||||||
chr1:21273346 | C | CGTGTGTG others(3): Show |
1 | a0001c0001t0002g0228 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.281-436_281-435ins others(10): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273346 | ||||||
chr1:21273346 | C | CGTGTGTG others(7): Show |
1 | a0001c0003t0002g0180 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.281-449_281-436dup others(14): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273346 | ||||||
chr1:21273346 | C | T | 1 | a0001c0001t0028g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.281-435G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273346 | ||||||
chr1:21273346 | CGT | C | 33 | a0001c0001t0001g0027a0001c0001t0001g0058a0001c0001t0001g0071others(30): Show | 33 | HG00323.hp2 HG00639.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.281-437_281-436del others(2): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273346 | ||||||
chr1:21273346 | CGTGT | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(78): Show | 86 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.281-439_281-436del others(4): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273346 | ||||||
chr1:21273346 | CGTGTGTG others(3): Show |
C | 1 | a0001c0002t0005g0242 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.281-445_281-436del others(10): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273346 | ||||||
chr1:21273348 | T | C | 1 | a0001c0001t0028g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.281-437A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273348 | ||||||
chr1:21273356 | T | C | 1 | a0001c0003t0003g0099 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.281-445A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273356 | ||||||
chr1:21273383 | A | C | 3 | a0001c0001t0003g0029a0001c0001t0003g0057a0001c0001t0030g0056 | 3 | HG00544.hp1 HG00673.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.281-472T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273383 | ||||||
chr1:21273496 | T | C | 1 | a0001c0002t0010g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.281-585A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273496 | ||||||
chr1:21273609 | T | C | 1 | a0001c0001t0033g0091 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.281-698A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273609 | ||||||
chr1:21273700 | C | T | 1 | a0001c0002t0009g0239 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.281-789G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273700 | ||||||
chr1:21273701 | G | A | 2 | a0001c0001t0002g0228a0001c0002t0009g0227 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.281-790C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273701 | ||||||
chr1:21273770 | G | A | 3 | a0001c0001t0001g0251a0001c0002t0004g0249a0001c0002t0004g0250 | 3 | HG01069.hp2 HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.281-859C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273770 | ||||||
chr1:21273843 | G | A | 2 | a0001c0001t0035g0097a0001c0002t0004g0098 | 2 | HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.281-932C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273843 | ||||||
chr1:21273942 | C | T | 1 | a0001c0002t0009g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.281-1031G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21273942 | ||||||
chr1:21274184 | G | A | 38 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(35): Show | 38 | HG01081.hp2 HG01175.hp1 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.281-1273C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21274184 | ||||||
chr1:21274393 | T | C | 2 | a0001c0001t0002g0228a0001c0002t0009g0227 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.281-1482A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21274393 | ||||||
chr1:21274605 | C | T | 2 | a0001c0001t0002g0228a0001c0002t0009g0227 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.281-1694G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21274605 | ||||||
chr1:21274742 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.281-1831T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21274742 | ||||||
chr1:21274804 | A | G | 3 | a0001c0001t0003g0288a0001c0002t0004g0256a0001c0002t0004g0285 | 3 | HG02145.hp2 HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.281-1893T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21274804 | ||||||
chr1:21274833 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.281-1922T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21274833 | ||||||
chr1:21275065 | T | C | 1 | a0003c0016t0023g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.281-2154A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21275065 | ||||||
chr1:21275245 | G | C | 1 | a0008c0015t0001g0030 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.281-2334C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21275245 | ||||||
chr1:21275255 | C | T | 7 | a0001c0001t0002g0228a0001c0001t0028g0294a0001c0002t0004g0084others(4): Show | 7 | HG01106.hp1 HG01109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.281-2344G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21275255 | ||||||
chr1:21275393 | G | C | 2 | a0001c0001t0003g0102a0001c0001t0003g0103 | 2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.281-2482C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21275393 | ||||||
chr1:21275452 | A | C | 6 | a0001c0001t0001g0191a0001c0001t0002g0109a0001c0001t0002g0190others(3): Show | 6 | HG02809.hp2 HG02922.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.281-2541T>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21275452 | ||||||
chr1:21275485 | C | G | 1 | a0001c0001t0018g0055 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.281-2574G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21275485 | ||||||
chr1:21275519 | C | T | 5 | a0001c0001t0002g0282a0001c0001t0007g0008a0001c0001t0007g0244others(2): Show | 6 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.281-2608G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21275519 | ||||||
chr1:21275550 | G | A | 5 | a0001c0001t0003g0148a0001c0001t0028g0294a0001c0002t0004g0084others(2): Show | 5 | HG01109.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-2639C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21275550 | ||||||
chr1:21275552 | G | A | 2 | a0001c0001t0002g0228a0001c0002t0009g0227 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.281-2641C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21275552 | ||||||
chr1:21275771 | T | C | 1 | a0006c0011t0003g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.281-2860A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21275771 | ||||||
chr1:21276026 | C | CT | 81 | a0001c0001t0001g0031a0001c0001t0001g0065a0001c0001t0001g0088others(78): Show | 82 | HG00639.hp1 HG00639.hp2 HG01099.hp2 others(79): Show |
intron_variant | MODIFIER | c.281-3116dupA | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276026 | ||||||
chr1:21276026 | C | CTT | 18 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0107others(15): Show | 18 | HG01069.hp2 HG01071.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.281-3117_281-3116d others(4): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276026 | ||||||
chr1:21276142 | C | T | 8 | a0001c0001t0001g0212a0001c0001t0006g0012a0001c0001t0006g0014others(5): Show | 9 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+3049G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276142 | ||||||
chr1:21276243 | C | G | 1 | a0001c0002t0012g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.280+2948G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276243 | ||||||
chr1:21276352 | C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0076 | 2 | HG01081.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.280+2839G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276352 | ||||||
chr1:21276370 | T | TA | 8 | a0001c0001t0001g0212a0001c0001t0006g0012a0001c0001t0006g0014others(5): Show | 9 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+2820dupT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276370 | ||||||
chr1:21276429 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.280+2762G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276429 | ||||||
chr1:21276532 | G | A | 1 | a0001c0003t0002g0171 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+2659C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276532 | ||||||
chr1:21276627 | G | A | 1 | a0002c0006t0016g0172 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.280+2564C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276627 | ||||||
chr1:21276680 | CTTT | C | 3 | a0001c0002t0004g0084a0001c0002t0014g0229a0001c0002t0014g0230 | 3 | HG01109.hp2 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.280+2508_280+2510d others(5): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276680 | ||||||
chr1:21276684 | C | A | 3 | a0001c0002t0004g0084a0001c0002t0014g0229a0001c0002t0014g0230 | 3 | HG01109.hp2 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.280+2507G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276684 | ||||||
chr1:21276684 | C | T | 1 | a0001c0001t0028g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.280+2507G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276684 | ||||||
chr1:21276684 | CT | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0136others(78): Show | 84 | HG00323.hp1 HG00609.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.280+2506delA | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276684 | ||||||
chr1:21276802 | C | T | 5 | a0001c0001t0001g0143a0001c0003t0001g0145a0001c0003t0001g0188others(2): Show | 5 | HG00735.hp1 HG01255.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+2389G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276802 | ||||||
chr1:21276874 | C | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(127): Show | 135 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.280+2317G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276874 | ||||||
chr1:21276905 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.280+2286G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21276905 | ||||||
chr1:21277007 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.280+2184A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277007 | ||||||
chr1:21277013 | C | T | 6 | a0001c0001t0003g0121a0001c0001t0007g0008a0001c0001t0007g0244others(3): Show | 7 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.280+2178G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277013 | ||||||
chr1:21277022 | T | C | 1 | a0007c0012t0003g0054 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.280+2169A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277022 | ||||||
chr1:21277050 | G | A | 4 | a0001c0001t0028g0294a0001c0002t0004g0084a0001c0002t0014g0229others(1): Show | 4 | HG01109.hp2 HG02280.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+2141C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277050 | ||||||
chr1:21277139 | C | T | 1 | a0001c0003t0002g0080 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.280+2052G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277139 | ||||||
chr1:21277164 | T | C | 1 | a0001c0001t0007g0275 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.280+2027A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277164 | ||||||
chr1:21277196 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.280+1995C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277196 | ||||||
chr1:21277332 | C | T | 5 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(2): Show | 6 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+1859G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277332 | ||||||
chr1:21277388 | T | C | 30 | a0001c0001t0001g0292a0001c0001t0002g0228a0001c0001t0002g0254others(27): Show | 31 | HG00639.hp2 HG01099.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.280+1803A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277388 | ||||||
chr1:21277570 | A | AAC | 6 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(3): Show | 7 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.280+1619_280+1620d others(4): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277570 | ||||||
chr1:21277604 | C | A | 3 | a0001c0001t0001g0251a0001c0002t0004g0249a0001c0002t0004g0250 | 3 | HG01069.hp2 HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.280+1587G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277604 | ||||||
chr1:21277617 | C | T | 1 | a0004c0014t0021g0141 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.280+1574G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277617 | ||||||
chr1:21277637 | C | G | 2 | a0001c0001t0035g0097a0001c0002t0004g0098 | 2 | HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.280+1554G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277637 | ||||||
chr1:21277678 | A | T | 1 | a0001c0001t0001g0140 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.280+1513T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277678 | ||||||
chr1:21277894 | C | G | 13 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0269others(10): Show | 13 | HG01069.hp1 HG01243.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.280+1297G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21277894 | ||||||
chr1:21278174 | T | C | 7 | a0001c0001t0003g0004a0001c0001t0003g0028a0001c0001t0003g0029others(4): Show | 8 | HG00544.hp1 HG00621.hp2 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.280+1017A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21278174 | ||||||
chr1:21278301 | T | C | 1 | a0001c0001t0002g0283 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.280+890A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21278301 | ||||||
chr1:21278316 | A | G | 3 | a0001c0003t0002g0120a0001c0003t0002g0139a0001c0003t0002g0211 | 3 | HG01258.hp1 HG02615.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.280+875T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21278316 | ||||||
chr1:21278486 | C | T | 1 | a0001c0002t0011g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.280+705G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21278486 | ||||||
chr1:21278547 | T | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(69): Show | 76 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.280+644A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21278547 | ||||||
chr1:21278604 | C | G | 1 | a0001c0001t0003g0173 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.280+587G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21278604 | ||||||
chr1:21278609 | G | C | 8 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0269others(5): Show | 8 | HG01069.hp1 HG01243.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.280+582C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21278609 | ||||||
chr1:21278706 | G | A | 1 | a0001c0001t0003g0203 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.280+485C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21278706 | ||||||
chr1:21278723 | T | C | 2 | a0001c0001t0002g0228a0001c0002t0009g0227 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.280+468A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21278723 | ||||||
chr1:21278830 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.280+361G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21278830 | ||||||
chr1:21278831 | G | C | 1 | a0001c0001t0028g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.280+360C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21278831 | ||||||
chr1:21278904 | T | C | 1 | a0009c0009t0002g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.280+287A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21278904 | ||||||
chr1:21278948 | G | A | 7 | a0001c0001t0002g0228a0001c0001t0028g0294a0001c0002t0004g0084others(4): Show | 7 | HG01106.hp1 HG01109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.280+243C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21278948 | ||||||
chr1:21279102 | G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060 | 3 | HG01952.hp2 HG02040.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.280+89C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 3/18 | chr1 | 21279102 | ||||||
chr1:21279497 | G | C | 1 | a0001c0001t0003g0061 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.139-165C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21279497 | ||||||
chr1:21279697 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.139-365C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21279697 | ||||||
chr1:21279788 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.139-456G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21279788 | ||||||
chr1:21279811 | C | T | 7 | a0001c0001t0006g0012a0001c0001t0006g0014a0001c0001t0006g0015others(4): Show | 8 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.139-479G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21279811 | ||||||
chr1:21279906 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.139-574C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21279906 | ||||||
chr1:21279923 | A | G | 1 | a0001c0001t0028g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.139-591T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21279923 | ||||||
chr1:21280289 | C | T | 10 | a0001c0001t0001g0251a0001c0001t0002g0228a0001c0001t0028g0294others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-957G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21280289 | ||||||
chr1:21280290 | G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(67): Show | 74 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.139-958C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21280290 | ||||||
chr1:21280414 | C | T | 1 | a0001c0002t0004g0257 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.139-1082G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21280414 | ||||||
chr1:21280417 | G | A | 1 | a0001c0001t0028g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.139-1085C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21280417 | ||||||
chr1:21280574 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.139-1242A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21280574 | ||||||
chr1:21280706 | G | C | 1 | a0001c0001t0003g0062 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.139-1374C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21280706 | ||||||
chr1:21280768 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.139-1436C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21280768 | ||||||
chr1:21280788 | G | A | 2 | a0001c0001t0002g0228a0001c0002t0009g0227 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.139-1456C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21280788 | ||||||
chr1:21280872 | A | G | 36 | a0001c0001t0001g0251a0001c0001t0001g0292a0001c0001t0002g0228others(33): Show | 37 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.139-1540T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21280872 | ||||||
chr1:21280931 | G | A | 1 | a0001c0001t0003g0138 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.139-1599C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21280931 | ||||||
chr1:21281025 | C | T | 1 | a0001c0001t0007g0275 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.139-1693G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281025 | ||||||
chr1:21281062 | C | A | 4 | a0001c0002t0004g0084a0001c0002t0014g0229a0001c0002t0014g0230others(1): Show | 4 | HG01106.hp1 HG01109.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-1730G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281062 | ||||||
chr1:21281082 | C | T | 1 | a0001c0001t0002g0276 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.139-1750G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281082 | ||||||
chr1:21281117 | G | C | 2 | a0001c0001t0002g0228a0001c0002t0009g0227 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.139-1785C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281117 | ||||||
chr1:21281131 | A | G | 3 | a0001c0001t0001g0251a0001c0002t0004g0249a0001c0002t0004g0250 | 3 | HG01069.hp2 HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.139-1799T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281131 | ||||||
chr1:21281168 | C | A | 1 | a0010c0018t0017g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.139-1836G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281168 | ||||||
chr1:21281184 | C | T | 3 | a0001c0001t0001g0251a0001c0002t0004g0249a0001c0002t0004g0250 | 3 | HG01069.hp2 HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.139-1852G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281184 | ||||||
chr1:21281191 | G | GAAAAC | 9 | a0001c0001t0001g0063a0001c0001t0001g0251a0001c0001t0002g0282others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-1864_139-1860d others(7): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281191 | ||||||
chr1:21281191 | G | GAAAACAA others(3): Show |
2 | a0001c0001t0028g0294a0001c0003t0003g0099 | 2 | HG01106.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.139-1869_139-1860d others(12): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281191 | ||||||
chr1:21281191 | G | GAAAACAA others(8): Show |
3 | a0001c0002t0004g0084a0001c0002t0014g0229a0001c0002t0014g0230 | 3 | HG01109.hp2 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.139-1874_139-1860d others(17): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281191 | ||||||
chr1:21281191 | G | GAAAACAA others(13): Show |
1 | a0001c0002t0009g0227 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.139-1879_139-1860d others(22): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281191 | ||||||
chr1:21281191 | G | GAAAACAA others(18): Show |
1 | a0001c0001t0002g0228 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.139-1884_139-1860d others(27): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281191 | ||||||
chr1:21281191 | GAAAACAA others(3): Show |
G | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG01256.hp2 HG01258.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-1869_139-1860d others(12): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281191 | ||||||
chr1:21281226 | C | G | 4 | a0001c0002t0011g0016a0001c0002t0012g0108a0001c0002t0012g0234others(1): Show | 4 | HG01884.hp2 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-1894G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281226 | ||||||
chr1:21281412 | G | A | 1 | a0001c0001t0002g0287 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.139-2080C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281412 | ||||||
chr1:21281563 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.139-2231C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281563 | ||||||
chr1:21281651 | T | C | 1 | a0001c0001t0028g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.139-2319A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281651 | ||||||
chr1:21281684 | G | GTGTTT | 4 | a0001c0001t0001g0006a0001c0001t0024g0210a0001c0002t0004g0256others(1): Show | 5 | HG01516.hp1 HG01517.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-2357_139-2353d others(7): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281684 | ||||||
chr1:21281762 | T | C | 8 | a0001c0001t0003g0200a0001c0001t0003g0202a0001c0001t0003g0203others(5): Show | 8 | HG02257.hp1 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.139-2430A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281762 | ||||||
chr1:21281765 | C | T | 3 | a0001c0001t0001g0251a0001c0002t0004g0249a0001c0002t0004g0250 | 3 | HG01069.hp2 HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.139-2433G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281765 | ||||||
chr1:21281857 | C | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(169): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.139-2525G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281857 | ||||||
chr1:21281975 | G | A | 1 | a0001c0001t0002g0228 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.139-2643C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21281975 | ||||||
chr1:21282035 | T | G | 1 | a0001c0002t0004g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.139-2703A>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282035 | ||||||
chr1:21282301 | A | G | 1 | a0001c0001t0003g0029 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.139-2969T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282301 | ||||||
chr1:21282332 | A | T | 1 | a0001c0001t0004g0289 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.139-3000T>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282332 | ||||||
chr1:21282519 | T | C | 2 | a0001c0001t0002g0105a0001c0001t0003g0106 | 2 | HG01081.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.139-3187A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282519 | ||||||
chr1:21282581 | C | T | 2 | a0001c0001t0002g0254a0001c0001t0002g0283 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.139-3249G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282581 | ||||||
chr1:21282588 | G | GA | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(153): Show | 162 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.139-3257dupT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282588 | ||||||
chr1:21282588 | G | GAA | 11 | a0001c0001t0001g0026a0001c0001t0001g0212a0001c0001t0002g0282others(8): Show | 12 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.139-3258_139-3257d others(4): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282588 | ||||||
chr1:21282768 | C | T | 2 | a0001c0002t0004g0256a0001c0002t0004g0285 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.139-3436G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282768 | ||||||
chr1:21282892 | C | G | 2 | a0001c0002t0004g0256a0001c0002t0004g0285 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.139-3560G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282892 | ||||||
chr1:21282937 | AT | A | 92 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0072others(89): Show | 95 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.139-3606delA | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282937 | ||||||
chr1:21282937 | ATT | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(158): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.139-3607_139-3606d others(4): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282937 | ||||||
chr1:21282940 | T | A | 1 | a0001c0001t0001g0178 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.139-3608A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282940 | ||||||
chr1:21282941 | T | A | 2 | a0001c0001t0013g0179a0001c0003t0002g0180 | 2 | HG01175.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.139-3609A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282941 | ||||||
chr1:21282942 | T | A | 28 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0107others(25): Show | 28 | HG01069.hp2 HG01071.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.139-3610A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282942 | ||||||
chr1:21282965 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.139-3633C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21282965 | ||||||
chr1:21283033 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.139-3701G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21283033 | ||||||
chr1:21283034 | C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0077 | 3 | HG00609.hp1 NA19062.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.139-3702G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21283034 | ||||||
chr1:21283158 | G | T | 8 | a0001c0001t0001g0212a0001c0001t0006g0012a0001c0001t0006g0014others(5): Show | 9 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-3826C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21283158 | ||||||
chr1:21283263 | GAATTTTT others(4): Show |
G | 8 | a0001c0001t0001g0212a0001c0001t0006g0012a0001c0001t0006g0014others(5): Show | 9 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-3942_139-3932d others(13): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21283263 | ||||||
chr1:21283273 | T | A | 8 | a0001c0001t0035g0097a0001c0002t0004g0084a0001c0002t0004g0098others(5): Show | 8 | HG01106.hp1 HG01109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.139-3941A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21283273 | ||||||
chr1:21283310 | G | A | 3 | a0001c0001t0001g0107a0001c0001t0002g0109a0001c0002t0012g0108 | 3 | HG02647.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.139-3978C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21283310 | ||||||
chr1:21283389 | G | T | 2 | a0001c0002t0005g0237a0001c0002t0005g0242 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.139-4057C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21283389 | ||||||
chr1:21283530 | C | A | 2 | a0001c0001t0002g0255a0001c0001t0003g0288 | 2 | HG02145.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.139-4198G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21283530 | ||||||
chr1:21283632 | C | G | 1 | a0009c0009t0002g0270 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.139-4300G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21283632 | ||||||
chr1:21283673 | C | A | 14 | a0001c0001t0001g0107a0001c0001t0001g0110a0001c0001t0001g0111others(11): Show | 14 | HG01081.hp2 HG02055.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.139-4341G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21283673 | ||||||
chr1:21283729 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.139-4397G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21283729 | ||||||
chr1:21283961 | A | G | 1 | a0001c0002t0012g0234 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.139-4629T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21283961 | ||||||
chr1:21284181 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.139-4849C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21284181 | ||||||
chr1:21284434 | G | A | 1 | a0010c0018t0017g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.139-5102C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21284434 | ||||||
chr1:21284533 | G | A | 9 | a0001c0001t0002g0254a0001c0001t0002g0271a0001c0001t0002g0276others(6): Show | 9 | HG00639.hp2 HG01243.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-5201C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21284533 | ||||||
chr1:21284712 | T | C | 26 | a0001c0001t0001g0292a0001c0001t0002g0254a0001c0001t0002g0255others(23): Show | 27 | HG00639.hp2 HG01099.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.138+5358A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21284712 | ||||||
chr1:21284774 | G | A | 2 | a0001c0001t0002g0183a0001c0001t0003g0184 | 2 | NA18975.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.138+5296C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21284774 | ||||||
chr1:21285075 | A | G | 1 | a0001c0002t0010g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.138+4995T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285075 | ||||||
chr1:21285184 | C | T | 7 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0002t0005g0237others(4): Show | 7 | HG01069.hp1 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.138+4886G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285184 | ||||||
chr1:21285329 | T | C | 3 | a0001c0001t0001g0251a0001c0002t0004g0249a0001c0002t0004g0250 | 3 | HG01069.hp2 HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.138+4741A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285329 | ||||||
chr1:21285398 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.138+4672C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285398 | ||||||
chr1:21285573 | C | A | 2 | a0001c0002t0004g0256a0001c0002t0004g0285 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.138+4497G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285573 | ||||||
chr1:21285689 | C | CA | 109 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0024others(106): Show | 114 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.138+4380dupT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285689 | ||||||
chr1:21285689 | C | CAA | 22 | a0001c0001t0001g0020a0001c0001t0001g0065a0001c0001t0001g0072others(19): Show | 22 | HG00621.hp2 HG01069.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.138+4379_138+4380d others(4): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285689 | ||||||
chr1:21285689 | CA | C | 19 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(16): Show | 19 | HG01175.hp1 HG02257.hp2 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.138+4380delT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285689 | ||||||
chr1:21285709 | A | AG | 5 | a0001c0001t0001g0251a0001c0002t0004g0214a0001c0002t0005g0231others(2): Show | 5 | HG02723.hp2 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+4360dupC | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285709 | ||||||
chr1:21285709 | A | G | 23 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(20): Show | 23 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.138+4361T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285709 | ||||||
chr1:21285758 | G | A | 3 | a0001c0001t0001g0292a0001c0001t0002g0290a0001c0002t0004g0291 | 3 | HG02055.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.138+4312C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285758 | ||||||
chr1:21285844 | T | C | 24 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(21): Show | 24 | HG01175.hp1 HG02257.hp2 HG02717.hp2 others(21): Show |
intron_variant | MODIFIER | c.138+4226A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285844 | ||||||
chr1:21285861 | G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0070a0001c0001t0001g0071others(2): Show | 5 | HG02040.hp1 HG02135.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+4209C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285861 | ||||||
chr1:21285905 | T | C | 4 | a0001c0002t0004g0214a0001c0002t0005g0231a0001c0002t0005g0232others(1): Show | 4 | HG02723.hp2 HG02965.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+4165A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285905 | ||||||
chr1:21285990 | C | CA | 12 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0079others(9): Show | 13 | HG01261.hp1 HG01884.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.138+4079dupT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285990 | ||||||
chr1:21285990 | C | CAA | 8 | a0001c0001t0001g0212a0001c0001t0006g0012a0001c0001t0006g0014others(5): Show | 9 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+4078_138+4079d others(4): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285990 | ||||||
chr1:21285990 | CA | C | 7 | a0001c0001t0001g0023a0001c0001t0001g0113a0001c0001t0002g0114others(4): Show | 7 | HG00323.hp1 HG00639.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.138+4079delT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21285990 | ||||||
chr1:21286463 | A | G | 2 | a0001c0002t0004g0265a0001c0002t0004g0266 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.138+3607T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21286463 | ||||||
chr1:21286515 | A | G | 2 | a0002c0004t0006g0002a0002c0004t0006g0010 | 3 | HG00140.hp1 HG02683.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.138+3555T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21286515 | ||||||
chr1:21286579 | G | C | 1 | a0001c0003t0003g0099 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.138+3491C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21286579 | ||||||
chr1:21286723 | G | A | 15 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0007g0008others(12): Show | 16 | HG01069.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.138+3347C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21286723 | ||||||
chr1:21286839 | T | A | 11 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0002t0005g0237others(8): Show | 11 | HG01069.hp1 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.138+3231A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21286839 | ||||||
chr1:21286915 | CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0010g0264 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.138+3142_138+3154d others(15): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21286915 | ||||||
chr1:21286924 | G | GA | 26 | a0001c0001t0001g0292a0001c0001t0002g0254a0001c0001t0002g0255others(23): Show | 27 | HG00639.hp2 HG01099.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.138+3145dupT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21286924 | ||||||
chr1:21287003 | C | T | 2 | a0001c0003t0002g0021a0001c0003t0002g0022 | 2 | NA18994.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.138+3067G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287003 | ||||||
chr1:21287170 | T | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0076 | 2 | HG01081.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.138+2900A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287170 | ||||||
chr1:21287252 | G | C | 2 | a0001c0001t0002g0228a0001c0002t0009g0227 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.138+2818C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287252 | ||||||
chr1:21287439 | T | C | 1 | a0010c0018t0017g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.138+2631A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287439 | ||||||
chr1:21287481 | G | A | 1 | a0001c0001t0028g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.138+2589C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287481 | ||||||
chr1:21287581 | C | T | 1 | a0010c0018t0017g0236 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.138+2489G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287581 | ||||||
chr1:21287622 | T | C | 1 | a0001c0003t0001g0208 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.138+2448A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287622 | ||||||
chr1:21287695 | T | C | 5 | a0001c0001t0007g0008a0001c0001t0007g0244a0001c0001t0007g0245others(2): Show | 6 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+2375A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287695 | ||||||
chr1:21287738 | G | A | 3 | a0001c0002t0004g0084a0001c0002t0014g0229a0001c0002t0014g0230 | 3 | HG01109.hp2 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.138+2332C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287738 | ||||||
chr1:21287960 | G | GA | 15 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(12): Show | 16 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.138+2109dupT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287960 | ||||||
chr1:21287960 | GA | G | 44 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(41): Show | 44 | HG01081.hp2 HG01106.hp1 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.138+2109delT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287960 | ||||||
chr1:21287961 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.138+2109T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287961 | ||||||
chr1:21287962 | A | G | 23 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(20): Show | 23 | HG01106.hp1 HG01175.hp1 HG02717.hp2 others(20): Show |
intron_variant | MODIFIER | c.138+2108T>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287962 | ||||||
chr1:21287971 | A | AC | 3 | a0001c0002t0004g0256a0001c0002t0012g0234a0001c0017t0020g0235 | 3 | HG01884.hp2 HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.138+2098_138+2099i others(3): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287971 | ||||||
chr1:21287971 | AAAC | A | 6 | a0001c0001t0001g0251a0001c0002t0004g0084a0001c0002t0004g0249others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+2096_138+2098d others(5): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21287971 | ||||||
chr1:21288088 | T | C | 5 | a0001c0002t0004g0214a0001c0002t0005g0231a0001c0002t0005g0232others(2): Show | 5 | HG02723.hp2 HG02965.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+1982A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21288088 | ||||||
chr1:21288190 | T | C | 7 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0003t0001g0216others(4): Show | 7 | HG00673.hp1 NA18612.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.138+1880A>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21288190 | ||||||
chr1:21288228 | G | A | 4 | a0001c0003t0002g0080a0001c0003t0002g0082a0001c0003t0002g0083others(1): Show | 4 | HG00140.hp2 HG00558.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+1842C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21288228 | ||||||
chr1:21288238 | C | T | 4 | a0001c0001t0003g0086a0001c0001t0003g0087a0001c0003t0001g0005others(1): Show | 5 | HG00738.hp1 HG01934.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+1832G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21288238 | ||||||
chr1:21288477 | C | T | 3 | a0001c0002t0004g0084a0001c0002t0014g0229a0001c0002t0014g0230 | 3 | HG01109.hp2 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.138+1593G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21288477 | ||||||
chr1:21288546 | C | A | 16 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0007g0008others(13): Show | 17 | HG01069.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.138+1524G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21288546 | ||||||
chr1:21288567 | G | C | 6 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG02717.hp2 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+1503C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21288567 | ||||||
chr1:21288681 | G | C | 2 | a0001c0002t0014g0229a0001c0002t0014g0230 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.138+1389C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21288681 | ||||||
chr1:21288686 | G | C | 2 | a0001c0002t0005g0231a0001c0002t0005g0232 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.138+1384C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21288686 | ||||||
chr1:21288732 | T | A | 16 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0007g0008others(13): Show | 17 | HG01069.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.138+1338A>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21288732 | ||||||
chr1:21288839 | C | A | 10 | a0001c0001t0001g0292a0001c0001t0002g0255a0001c0001t0002g0286others(7): Show | 11 | HG01099.hp1 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.138+1231G>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21288839 | ||||||
chr1:21288897 | CA | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0020others(65): Show | 72 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.138+1172delT | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21288897 | ||||||
chr1:21289021 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.138+1049G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21289021 | ||||||
chr1:21289051 | A | AAGAGGCG others(23): Show |
1 | a0001c0003t0002g0019 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.138+989_138+1018du others(31): Show |
ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21289051 | ||||||
chr1:21289066 | G | A | 15 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0007g0008others(12): Show | 16 | HG01069.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.138+1004C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21289066 | ||||||
chr1:21289192 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138+878G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21289192 | ||||||
chr1:21289436 | C | G | 1 | a0001c0001t0003g0018 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.138+634G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21289436 | ||||||
chr1:21289481 | G | T | 1 | a0001c0001t0002g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.138+589C>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21289481 | ||||||
chr1:21289594 | G | C | 2 | a0001c0001t0008g0247a0001c0001t0008g0248 | 2 | NA18960.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.138+476C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21289594 | ||||||
chr1:21289695 | C | G | 1 | a0001c0001t0013g0017 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.138+375G>C | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21289695 | ||||||
chr1:21289768 | C | T | 1 | a0001c0002t0011g0016 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.138+302G>A | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21289768 | ||||||
chr1:21289860 | G | A | 3 | a0001c0001t0001g0251a0001c0002t0004g0249a0001c0002t0004g0250 | 3 | HG01069.hp2 HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.138+210C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21289860 | ||||||
chr1:21289920 | G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.138+150C>T | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21289920 | ||||||
chr1:21289940 | G | C | 41 | a0001c0001t0001g0269a0001c0001t0001g0292a0001c0001t0002g0254others(38): Show | 42 | HG00639.hp2 HG01099.hp1 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.138+130C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21289940 | ||||||
chr1:21290031 | G | C | 1 | a0001c0001t0028g0294 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.138+39C>G | ECE1 | ENSG00000117298.16 | transcript | ENST00000374893.11 | protein_coding | 2/18 | chr1 | 21290031 |