geneid | 129080 |
---|---|
ensemblid | ENSG00000186998.16 |
hgncid | 18036 |
symbol | EMID1 |
name | EMI domain containing 1 |
refseq_nuc | NM_133455.4 |
refseq_prot | NP_597712.2 |
ensembl_nuc | ENST00000334018.11 |
ensembl_prot | ENSP00000335481.6 |
mane_status | MANE Select |
chr | chr22 |
start | 29205896 |
end | 29259597 |
strand | + |
ver | v1.2 |
region | chr22:29205896-29259597 |
region5000 | chr22:29200896-29264597 |
regionname0 | EMID1_chr22_29205896_29259597 |
regionname5000 | EMID1_chr22_29200896_29264597 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 443 | 144 | 55 | 13 | 65 | 1 | 10 | 47 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0002 | 1/1 | 443 | 143 | 19 | 28 | 52 | 9 | 33 | 40 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0003 | 0/0 | 443 | 37 | 16 | 2 | 19 | 0 | 0 | 16 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0004 | 0/0 | 443 | 22 | 3 | 7 | 12 | 0 | 0 | 11 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0005 | 0/0 | 443 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0006 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1332 | 142 | 19 | 28 | 52 | 9 | 32 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
c0002 | 0/0 | 1332 | 142 | 53 | 13 | 65 | 1 | 10 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
c0003 | 0/0 | 1332 | 37 | 16 | 2 | 19 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
c0004 | 0/0 | 1332 | 22 | 3 | 7 | 12 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
c0005 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
c0006 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
c0007 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
c0008 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
c0009 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 797 | 145 | 30 | 29 | 49 | 5 | 31 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
t0002 | 0/0 | 797 | 104 | 36 | 14 | 43 | 3 | 8 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
t0003 | 1/0 | 797 | 80 | 14 | 7 | 53 | 2 | 3 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
t0004 | 0/0 | 797 | 6 | 6 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
t0005 | 0/0 | 797 | 4 | 4 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
t0006 | 0/0 | 797 | 2 | 2 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
t0007 | 0/0 | 797 | 2 | 0 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
t0008 | 0/0 | 797 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
t0009 | 0/0 | 797 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
t0010 | 0/0 | 797 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
t0011 | 0/0 | 797 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
t0012 | 0/0 | 797 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0023 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0268 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 1332 | 142 | 53 | 13 | 65 | 1 | 10 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0001c0008 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0001c0009 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0002c0001 | 1/1 | 1332 | 142 | 19 | 28 | 52 | 9 | 32 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0002c0005 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0003c0003 | 0/0 | 1332 | 37 | 16 | 2 | 19 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0004c0004 | 0/0 | 1332 | 22 | 3 | 7 | 12 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0005c0006 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0006c0007 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 2128 | 53 | 19 | 5 | 21 | 0 | 8 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0001c0002t0002 | 0/0 | 2128 | 63 | 23 | 7 | 31 | 1 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0001c0002t0003 | 0/0 | 2128 | 17 | 2 | 1 | 13 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0001c0002t0004 | 0/0 | 2128 | 6 | 6 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0001c0002t0006 | 0/0 | 2128 | 2 | 2 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0001c0002t0011 | 0/0 | 2128 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0001c0008t0002 | 0/0 | 2128 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0001c0009t0001 | 0/0 | 2128 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0002c0001t0001 | 0/1 | 2128 | 79 | 4 | 20 | 27 | 5 | 22 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0002c0001t0002 | 0/0 | 2128 | 33 | 9 | 7 | 8 | 2 | 7 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0002c0001t0003 | 1/0 | 2128 | 24 | 5 | 1 | 14 | 2 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0002c0001t0007 | 0/0 | 2128 | 2 | 0 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0002c0001t0008 | 0/0 | 2128 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0002c0001t0009 | 0/0 | 2128 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0002c0001t0010 | 0/0 | 2128 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0002c0001t0012 | 0/0 | 2128 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0002c0005t0001 | 0/0 | 2128 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0003c0003t0001 | 0/0 | 2128 | 9 | 6 | 2 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0003c0003t0002 | 0/0 | 2128 | 4 | 2 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0003c0003t0003 | 0/0 | 2128 | 20 | 4 | 0 | 16 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0003c0003t0005 | 0/0 | 2128 | 4 | 4 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0004c0004t0001 | 0/0 | 2128 | 2 | 0 | 2 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0004c0004t0002 | 0/0 | 2128 | 3 | 1 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0004c0004t0003 | 0/0 | 2128 | 17 | 2 | 5 | 10 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0005c0006t0003 | 0/0 | 2128 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
a0006c0007t0003 | 0/0 | 2128 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | copy fasta | chr22 | 29200896 | 29264597 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0003g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0002t0011g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0008t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0001c0009t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0023 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0268 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0009g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0010g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0001t0012g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0002c0005t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0003c0003t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0004c0004t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0005c0006t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
a0006c0007t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0003 | g0339 | EUR | GBR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00099 | hp2 | a0002 | c0001 | t0002 | g0053 | EUR | GBR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00140 | hp1 | a0002 | c0001 | t0001 | g0092 | EUR | GBR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00140 | hp2 | a0002 | c0001 | t0001 | g0165 | EUR | GBR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0330 | EUR | FIN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00280 | hp2 | a0002 | c0001 | t0003 | g0217 | EUR | FIN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00423 | hp1 | a0002 | c0001 | t0002 | g0122 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00438 | hp1 | a0004 | c0004 | t0002 | g0119 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00544 | hp1 | a0002 | c0001 | t0001 | g0135 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00558 | hp2 | a0001 | c0002 | t0003 | g0061 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00597 | hp1 | a0001 | c0002 | t0003 | g0179 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00609 | hp1 | a0002 | c0001 | t0001 | g0090 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00609 | hp2 | a0002 | c0001 | t0003 | g0101 | EAS | CHS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00639 | hp1 | a0004 | c0004 | t0003 | g0215 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00639 | hp2 | a0002 | c0001 | t0002 | g0148 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00642 | hp1 | a0002 | c0001 | t0001 | g0039 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00642 | hp2 | a0004 | c0004 | t0003 | g0082 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00733 | hp1 | a0004 | c0004 | t0001 | g0213 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00733 | hp2 | a0002 | c0001 | t0001 | g0141 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00741 | hp1 | a0003 | c0003 | t0001 | g0226 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0094 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01070 | hp1 | a0002 | c0001 | t0001 | g0078 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01070 | hp2 | a0002 | c0001 | t0001 | g0293 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01074 | hp2 | a0004 | c0004 | t0003 | g0071 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01081 | hp2 | a0002 | c0001 | t0001 | g0010 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01099 | hp1 | a0002 | c0001 | t0003 | g0099 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0343 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01109 | hp1 | a0002 | c0001 | t0001 | g0009 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01109 | hp2 | a0002 | c0001 | t0002 | g0150 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01167 | hp1 | a0002 | c0001 | t0001 | g0166 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01167 | hp2 | a0004 | c0004 | t0003 | g0081 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01175 | hp1 | a0002 | c0001 | t0001 | g0080 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01175 | hp2 | a0004 | c0004 | t0003 | g0216 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0285 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0223 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01243 | hp1 | a0002 | c0001 | t0002 | g0286 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0304 | AMR | PUR | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01255 | hp1 | a0002 | c0001 | t0001 | g0140 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01256 | hp1 | a0002 | c0001 | t0001 | g0007 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01256 | hp2 | a0002 | c0001 | t0001 | g0068 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01257 | hp1 | a0002 | c0001 | t0001 | g0008 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01257 | hp2 | a0002 | c0001 | t0001 | g0048 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01258 | hp1 | a0002 | c0001 | t0001 | g0089 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01258 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01261 | hp2 | a0004 | c0004 | t0001 | g0057 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01346 | hp2 | a0002 | c0001 | t0001 | g0049 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01361 | hp1 | a0002 | c0001 | t0001 | g0270 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01361 | hp2 | a0002 | c0001 | t0002 | g0146 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01433 | hp1 | a0002 | c0001 | t0002 | g0120 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01433 | hp2 | a0002 | c0001 | t0001 | g0079 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01496 | hp1 | a0003 | c0003 | t0001 | g0320 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0197 | AMR | CLM | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01515 | hp1 | a0002 | c0001 | t0001 | g0272 | EUR | IBS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01515 | hp2 | a0002 | c0001 | t0001 | g0162 | EUR | IBS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01517 | hp1 | a0002 | c0001 | t0001 | g0273 | EUR | IBS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01517 | hp2 | a0002 | c0001 | t0002 | g0051 | EUR | IBS | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0291 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0192 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01891 | hp1 | a0003 | c0003 | t0003 | g0292 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01993 | hp1 | a0002 | c0001 | t0001 | g0087 | AMR | PEL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0228 | AMR | PEL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02004 | hp1 | a0002 | c0001 | t0002 | g0096 | AMR | PEL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0227 | AMR | PEL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02015 | hp1 | a0003 | c0003 | t0003 | g0260 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02015 | hp2 | a0002 | c0001 | t0001 | g0225 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02027 | hp2 | a0002 | c0001 | t0001 | g0163 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02040 | hp2 | a0002 | c0001 | t0003 | g0065 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0289 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02055 | hp2 | a0003 | c0003 | t0001 | g0319 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02071 | hp1 | a0002 | c0001 | t0012 | g0100 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02071 | hp2 | a0001 | c0002 | t0003 | g0261 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02080 | hp1 | a0002 | c0001 | t0001 | g0314 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02132 | hp1 | a0002 | c0001 | t0002 | g0073 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02132 | hp2 | a0001 | c0002 | t0003 | g0218 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02145 | hp1 | a0001 | c0002 | t0003 | g0316 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02145 | hp2 | a0003 | c0003 | t0005 | g0324 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02148 | hp1 | a0002 | c0001 | t0001 | g0341 | AMR | PEL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02148 | hp2 | a0002 | c0001 | t0002 | g0230 | AMR | PEL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02257 | hp1 | a0002 | c0001 | t0003 | g0337 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02257 | hp2 | a0002 | c0001 | t0002 | g0267 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02258 | hp1 | a0003 | c0003 | t0001 | g0333 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02258 | hp2 | a0002 | c0001 | t0002 | g0144 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0288 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0303 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0196 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02523 | hp1 | a0003 | c0003 | t0003 | g0205 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | KHV | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02572 | hp1 | a0002 | c0001 | t0003 | g0338 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02572 | hp2 | a0002 | c0001 | t0010 | g0310 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02602 | hp1 | a0002 | c0001 | t0001 | g0075 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0269 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02622 | hp1 | a0001 | c0008 | t0002 | g0047 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02622 | hp2 | a0002 | c0001 | t0002 | g0295 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02630 | hp2 | a0001 | c0002 | t0006 | g0198 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02647 | hp1 | a0001 | c0002 | t0004 | g0001 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02647 | hp2 | a0002 | c0001 | t0001 | g0284 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0340 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0255 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0331 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02698 | hp2 | a0002 | c0001 | t0002 | g0151 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0290 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02717 | hp2 | a0001 | c0002 | t0004 | g0001 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0038 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0305 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02738 | hp1 | a0002 | c0005 | t0001 | g0278 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02738 | hp2 | a0002 | c0001 | t0001 | g0275 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0297 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02818 | hp1 | a0006 | c0007 | t0003 | g0187 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0199 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0035 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02886 | hp2 | a0004 | c0004 | t0003 | g0306 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02895 | hp1 | a0002 | c0001 | t0002 | g0022 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02896 | hp1 | a0003 | c0003 | t0003 | g0016 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0190 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02897 | hp1 | a0002 | c0001 | t0002 | g0021 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02897 | hp2 | a0003 | c0003 | t0003 | g0015 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0200 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0204 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0238 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03017 | hp1 | a0002 | c0001 | t0001 | g0050 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03017 | hp2 | a0002 | c0001 | t0002 | g0280 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03041 | hp1 | a0004 | c0004 | t0002 | g0323 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03041 | hp2 | a0002 | c0001 | t0003 | g0336 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03098 | hp1 | a0001 | c0002 | t0011 | g0307 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03098 | hp2 | a0001 | c0002 | t0004 | g0026 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0300 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03130 | hp2 | a0002 | c0001 | t0002 | g0011 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03195 | hp1 | a0002 | c0001 | t0003 | g0311 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03209 | hp1 | a0002 | c0001 | t0001 | g0294 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0191 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03225 | hp1 | a0001 | c0002 | t0004 | g0025 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03225 | hp2 | a0003 | c0003 | t0001 | g0335 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03239 | hp1 | a0002 | c0001 | t0001 | g0149 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03239 | hp2 | a0002 | c0001 | t0001 | g0279 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03486 | hp1 | a0001 | c0002 | t0006 | g0020 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03486 | hp2 | a0002 | c0001 | t0002 | g0287 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03490 | hp1 | a0002 | c0001 | t0002 | g0054 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03490 | hp2 | a0002 | c0001 | t0001 | g0005 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03491 | hp1 | a0002 | c0001 | t0009 | g0243 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03491 | hp2 | a0002 | c0001 | t0002 | g0308 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03492 | hp1 | a0002 | c0001 | t0001 | g0005 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03492 | hp2 | a0002 | c0001 | t0002 | g0299 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0317 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0302 | AFR | ESN | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03540 | hp1 | a0002 | c0001 | t0003 | g0033 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03540 | hp2 | a0002 | c0001 | t0002 | g0220 | AFR | GWD | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03579 | hp1 | a0003 | c0003 | t0005 | g0322 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03579 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0237 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03654 | hp2 | a0002 | c0001 | t0001 | g0056 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0124 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03669 | hp2 | a0002 | c0001 | t0001 | g0164 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03704 | hp1 | a0002 | c0001 | t0001 | g0264 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03704 | hp2 | a0002 | c0001 | t0002 | g0069 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0256 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03710 | hp2 | a0002 | c0001 | t0001 | g0041 | SAS | PJL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03831 | hp1 | a0002 | c0001 | t0001 | g0074 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03831 | hp2 | a0002 | c0001 | t0001 | g0134 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03927 | hp1 | a0002 | c0001 | t0003 | g0109 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0271 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03942 | hp1 | a0002 | c0001 | t0002 | g0253 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03942 | hp2 | a0002 | c0001 | t0001 | g0098 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG04115 | hp1 | a0002 | c0001 | t0001 | g0274 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG04115 | hp2 | a0001 | c0002 | t0003 | g0259 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG04184 | hp1 | a0002 | c0001 | t0001 | g0276 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG04184 | hp2 | a0002 | c0001 | t0001 | g0265 | SAS | BEB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG04199 | hp1 | a0002 | c0001 | t0001 | g0115 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG04199 | hp2 | a0002 | c0001 | t0001 | g0064 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG04204 | hp1 | a0002 | c0001 | t0001 | g0257 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0236 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG04228 | hp1 | a0002 | c0001 | t0001 | g0342 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG04228 | hp2 | a0002 | c0001 | t0008 | g0263 | SAS | STU | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18522 | hp1 | a0003 | c0003 | t0005 | g0283 | AFR | YRI | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18522 | hp2 | a0003 | c0003 | t0002 | g0321 | AFR | YRI | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18612 | hp1 | a0002 | c0001 | t0001 | g0240 | EAS | CHB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18612 | hp2 | a0002 | c0001 | t0001 | g0070 | EAS | CHB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18747 | hp1 | a0001 | c0002 | t0003 | g0214 | EAS | CHB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18747 | hp2 | a0003 | c0003 | t0001 | g0210 | EAS | CHB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0301 | AFR | YRI | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18906 | hp2 | a0003 | c0003 | t0005 | g0282 | AFR | YRI | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18939 | hp1 | a0002 | c0001 | t0003 | g0107 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18939 | hp2 | a0002 | c0001 | t0002 | g0167 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18940 | hp1 | a0004 | c0004 | t0002 | g0145 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18942 | hp2 | a0002 | c0001 | t0001 | g0158 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18944 | hp2 | a0004 | c0004 | t0003 | g0113 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18945 | hp1 | a0003 | c0003 | t0003 | g0086 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18947 | hp1 | a0003 | c0003 | t0003 | g0139 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18947 | hp2 | a0002 | c0001 | t0001 | g0169 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18948 | hp2 | a0002 | c0001 | t0002 | g0246 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18951 | hp2 | a0002 | c0001 | t0001 | g0296 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18953 | hp1 | a0003 | c0003 | t0003 | g0067 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18953 | hp2 | a0003 | c0003 | t0003 | g0208 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18954 | hp1 | a0002 | c0001 | t0001 | g0154 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18954 | hp2 | a0003 | c0003 | t0003 | g0058 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18957 | hp1 | a0002 | c0001 | t0001 | g0153 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18957 | hp2 | a0002 | c0001 | t0002 | g0106 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18959 | hp2 | a0004 | c0004 | t0003 | g0221 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18960 | hp2 | a0003 | c0003 | t0003 | g0168 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18963 | hp1 | a0002 | c0001 | t0003 | g0129 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18964 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18964 | hp2 | a0002 | c0001 | t0001 | g0235 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18966 | hp1 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18966 | hp2 | a0002 | c0001 | t0003 | g0131 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18969 | hp1 | a0001 | c0002 | t0003 | g0121 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18969 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18970 | hp1 | a0002 | c0001 | t0007 | g0138 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18973 | hp2 | a0004 | c0004 | t0003 | g0185 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18974 | hp1 | a0004 | c0004 | t0003 | g0114 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18974 | hp2 | a0002 | c0001 | t0001 | g0329 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18977 | hp2 | a0002 | c0001 | t0003 | g0328 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18979 | hp1 | a0003 | c0003 | t0003 | g0084 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18979 | hp2 | a0002 | c0001 | t0003 | g0128 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18980 | hp1 | a0002 | c0001 | t0002 | g0062 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18980 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18981 | hp1 | a0001 | c0002 | t0003 | g0055 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18982 | hp2 | a0002 | c0001 | t0003 | g0241 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18985 | hp1 | a0003 | c0003 | t0003 | g0088 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18985 | hp2 | a0001 | c0002 | t0002 | g0332 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18986 | hp1 | a0002 | c0001 | t0003 | g0130 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18986 | hp2 | a0004 | c0004 | t0003 | g0118 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18990 | hp1 | a0003 | c0003 | t0003 | g0298 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18990 | hp2 | a0003 | c0003 | t0003 | g0181 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18993 | hp1 | a0004 | c0004 | t0003 | g0209 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18993 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18994 | hp1 | a0002 | c0001 | t0001 | g0262 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18994 | hp2 | a0002 | c0001 | t0007 | g0161 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18995 | hp2 | a0001 | c0002 | t0003 | g0233 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18998 | hp2 | a0004 | c0004 | t0003 | g0103 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19000 | hp2 | a0001 | c0002 | t0003 | g0142 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19004 | hp2 | a0003 | c0003 | t0003 | g0222 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19005 | hp2 | a0003 | c0003 | t0002 | g0085 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19009 | hp1 | a0002 | c0001 | t0001 | g0254 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19009 | hp2 | a0002 | c0001 | t0001 | g0327 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19010 | hp1 | a0004 | c0004 | t0003 | g0132 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19010 | hp2 | a0002 | c0001 | t0001 | g0110 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19011 | hp1 | a0002 | c0001 | t0003 | g0045 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19011 | hp2 | a0002 | c0001 | t0001 | g0171 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19012 | hp1 | a0004 | c0004 | t0003 | g0104 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19012 | hp2 | a0002 | c0001 | t0001 | g0156 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0242 | AFR | LWK | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0266 | AFR | LWK | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0277 | AFR | LWK | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19043 | hp2 | a0001 | c0009 | t0001 | g0281 | AFR | LWK | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19065 | hp1 | a0002 | c0001 | t0001 | g0136 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19065 | hp2 | a0002 | c0001 | t0003 | g0111 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19066 | hp1 | a0002 | c0001 | t0001 | g0176 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19066 | hp2 | a0002 | c0001 | t0001 | g0170 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19079 | hp1 | a0002 | c0001 | t0001 | g0157 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19081 | hp2 | a0003 | c0003 | t0002 | g0040 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19083 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19083 | hp2 | a0002 | c0001 | t0001 | g0155 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19084 | hp1 | a0002 | c0001 | t0003 | g0232 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19084 | hp2 | a0002 | c0001 | t0001 | g0133 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19085 | hp1 | a0004 | c0004 | t0003 | g0172 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19085 | hp2 | a0002 | c0001 | t0002 | g0102 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19087 | hp1 | a0002 | c0001 | t0001 | g0244 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19088 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19091 | hp1 | a0003 | c0003 | t0003 | g0180 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19091 | hp2 | a0002 | c0001 | t0002 | g0112 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19240 | hp1 | a0003 | c0003 | t0001 | g0028 | AFR | YRI | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | YRI | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA20129 | hp1 | a0003 | c0003 | t0001 | g0334 | AFR | ASW | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA20129 | hp2 | a0002 | c0001 | t0001 | g0312 | AFR | ASW | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA20905 | hp1 | a0002 | c0001 | t0001 | g0152 | SAS | GIH | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA20905 | hp2 | a0005 | c0006 | t0003 | g0066 | SAS | GIH | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0219 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02109 | hp2 | a0001 | c0002 | t0004 | g0027 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0032 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02486 | hp2 | a0004 | c0004 | t0003 | g0083 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0315 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG02559 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | ACB | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03471 | hp1 | a0002 | c0001 | t0002 | g0309 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG03471 | hp2 | a0003 | c0003 | t0002 | g0325 | AFR | MSL | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG06807 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | USA | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
HG06807 | hp2 | a0003 | c0003 | t0001 | g0318 | AFR | USA | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18955 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0147 | AFR | USA | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | USA | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA21309 | hp1 | a0003 | c0003 | t0003 | g0224 | AFR | LWK | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | LWK | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0001 | g0023 | REF | REF | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
homoSapiens_grch38 | hp1 | a0002 | c0001 | t0003 | g0268 | REF | REF | EMID1_chr22_29200896_29264597 | EMID1 | chr22 | 29200896 | 29264597 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:29225139
|
C | G | 4 | a0001a0003a0005others(1): Show | 183 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(180): Show |
missense_variant | MODERATE | c.326C>G | p.Ala109Gly | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/15 | 469/2128 | 326/1332 | 109/443 | chr22 | 29225139 | ||
chr22:29232285
|
C | T | 1 | a0006 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.706C>T | p.Arg236Trp | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/15 | 849/2128 | 706/1332 | 236/443 | chr22 | 29232285 | ||
chr22:29232304
|
C | T | 1 | a0005 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.725C>T | p.Thr242Ile | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/15 | 868/2128 | 725/1332 | 242/443 | chr22 | 29232304 | ||
chr22:29234348
|
G | A | 3 | a0003a0004a0005 | 60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
missense_variant&splice_region_variant | MODERATE | c.1073G>A | p.Arg358Gln | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/15 | 1216/2128 | 1073/1332 | 358/443 | chr22 | 29234348 | ||
chr22:29258907
|
G | A | 1 | a0006 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1295G>A | p.Arg432Gln | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 1438/2128 | 1295/1332 | 432/443 | chr22 | 29258907 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:29231121
|
C | T | 1 | a0001c0009 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.567C>T | p.Pro189Pro | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/15 | 710/2128 | 567/1332 | 189/443 | chr22 | 29231121 | ||
chr22:29231618
|
C | T | 1 | a0001c0008 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.612C>T | p.Pro204Pro | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 7/15 | 755/2128 | 612/1332 | 204/443 | chr22 | 29231618 | ||
chr22:29232275
|
G | A | 1 | a0002c0005 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.696G>A | p.Gly232Gly | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/15 | 839/2128 | 696/1332 | 232/443 | chr22 | 29232275 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:29205912
|
C | T | 2 | a0002c0001t0007a0002c0001t0012 | 3 | HG02071.hp1 NA18970.hp1 NA18994.hp2 |
5_prime_UTR_variant | MODIFIER | c.-127C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/15 | 127 | chr22 | 29205912 | |||||
chr22:29205916
|
C | T | 1 | a0001c0002t0011 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-123C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/15 | 123 | chr22 | 29205916 | |||||
chr22:29206020
|
G | A | 1 | a0001c0002t0004 | 6 | HG02109.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-19G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/15 | 19 | chr22 | 29206020 | |||||
chr22:29258957
|
C | T | 1 | a0001c0002t0006 | 2 | HG02630.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*13C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 13 | chr22 | 29258957 | |||||
chr22:29259272
|
G | C | 1 | a0002c0001t0008 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*328G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 328 | chr22 | 29259272 | |||||
chr22:29259320
|
C | G | 1 | a0002c0001t0010 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*376C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 376 | chr22 | 29259320 | |||||
chr22:29259382
|
C | T | 20 | a0001c0002t0001a0001c0002t0002a0001c0002t0004others(17): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*438C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 438 | chr22 | 29259382 | |||||
chr22:29259427
|
C | T | 13 | a0001c0002t0002a0001c0002t0004a0001c0002t0006others(10): Show | 121 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*483C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 483 | chr22 | 29259427 | |||||
chr22:29259506
|
G | A | 2 | a0001c0002t0011a0003c0003t0005 | 5 | HG02145.hp2 HG03098.hp1 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*562G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 562 | chr22 | 29259506 | |||||
chr22:29259550
|
G | A | 1 | a0002c0001t0009 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*606G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 15/15 | 606 | chr22 | 29259550 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:29206147
|
C | T | 6 | a0001c0002t0001g0340a0001c0002t0003g0343a0002c0001t0001g0005others(3): Show | 7 | HG00099.hp1 HG01099.hp2 HG02148.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.101+8C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206147 | ||||||
chr22:29206170
|
T | C | 5 | a0002c0001t0001g0006a0002c0001t0001g0007a0002c0001t0001g0008others(2): Show | 5 | HG01081.hp2 HG01109.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+31T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206170 | ||||||
chr22:29206250
|
T | TGAG | 12 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(9): Show | 12 | HG01081.hp1 HG01255.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.101+113_101+115dup others(3): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 29206250 | |||||
chr22:29206265
|
G | A | 1 | a0002c0001t0001g0023 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.101+126G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206265 | ||||||
chr22:29206500
|
C | T | 6 | a0002c0001t0003g0336a0002c0001t0003g0337a0002c0001t0003g0338others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+361C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206500 | ||||||
chr22:29206503
|
C | G | 7 | a0001c0002t0001g0326a0001c0002t0001g0331a0001c0002t0002g0330others(4): Show | 7 | HG00280.hp1 HG02698.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+364C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206503 | ||||||
chr22:29206663
|
A | G | 11 | a0001c0002t0001g0315a0001c0002t0002g0317a0001c0002t0003g0316others(8): Show | 11 | HG01496.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+524A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206663 | ||||||
chr22:29206700
|
C | T | 1 | a0002c0001t0001g0314 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.101+561C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206700 | ||||||
chr22:29206801
|
C | T | 1 | a0001c0002t0001g0313 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.101+662C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206801 | ||||||
chr22:29206930
|
T | C | 6 | a0001c0002t0004g0001a0001c0002t0004g0024a0001c0002t0004g0025others(3): Show | 7 | HG02109.hp2 HG02258.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+791T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206930 | ||||||
chr22:29206933
|
T | C | 11 | a0001c0002t0001g0030a0001c0002t0001g0036a0001c0002t0001g0037others(8): Show | 11 | HG02486.hp1 HG02723.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+794T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206933 | ||||||
chr22:29206982
|
G | A | 159 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0060others(156): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.101+843G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29206982 | ||||||
chr22:29207007
|
G | A | 1 | a0004c0004t0003g0185 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.101+868G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207007 | ||||||
chr22:29207079
|
G | A | 1 | a0001c0002t0002g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.101+940G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207079 | ||||||
chr22:29207092
|
C | A | 3 | a0001c0002t0001g0315a0001c0002t0002g0317a0001c0002t0003g0316 | 3 | HG02145.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.101+953C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207092 | ||||||
chr22:29207266
|
G | A | 6 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(3): Show | 6 | HG01884.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+1127G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207266 | ||||||
chr22:29207320
|
G | T | 1 | a0002c0001t0001g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101+1181G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207320 | ||||||
chr22:29207494
|
CTCAGAAA | C | 5 | a0001c0002t0004g0001a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 6 | HG02109.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.101+1358_101+1364d others(9): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 29207494 | |||||
chr22:29207552
|
G | A | 22 | a0001c0002t0002g0193a0001c0002t0002g0194a0001c0002t0002g0195others(19): Show | 22 | HG00408.hp1 HG00558.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.101+1413G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207552 | ||||||
chr22:29207622
|
A | G | 219 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0060others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.101+1483A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207622 | ||||||
chr22:29207636
|
A | G | 1 | a0003c0003t0001g0210 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.101+1497A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207636 | ||||||
chr22:29207644
|
G | T | 3 | a0002c0001t0002g0309a0002c0001t0003g0311a0002c0001t0010g0310 | 3 | HG02572.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.101+1505G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207644 | ||||||
chr22:29207757
|
C | T | 21 | a0001c0002t0002g0193a0001c0002t0002g0194a0001c0002t0002g0195others(18): Show | 21 | HG00408.hp1 HG00558.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.101+1618C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207757 | ||||||
chr22:29207807
|
G | A | 300 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(297): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.101+1668G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207807 | ||||||
chr22:29207875
|
G | A | 7 | a0001c0002t0001g0315a0001c0002t0002g0317a0001c0002t0003g0316others(4): Show | 7 | HG02145.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+1736G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207875 | ||||||
chr22:29207918
|
G | C | 10 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(7): Show | 10 | HG01081.hp1 HG01255.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+1779G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29207918 | ||||||
chr22:29208141
|
A | G | 56 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(53): Show | 57 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.101+2002A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208141 | ||||||
chr22:29208158
|
C | G | 6 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(3): Show | 6 | HG01884.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+2019C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208158 | ||||||
chr22:29208286
|
G | C | 181 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0060others(178): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.101+2147G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208286 | ||||||
chr22:29208321
|
C | T | 24 | a0001c0002t0001g0229a0001c0002t0001g0234a0001c0002t0002g0186others(21): Show | 24 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.101+2182C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208321 | ||||||
chr22:29208375
|
C | T | 1 | a0002c0001t0001g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.101+2236C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208375 | ||||||
chr22:29208572
|
G | A | 187 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0060others(184): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.101+2433G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208572 | ||||||
chr22:29208798
|
T | C | 243 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(240): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.101+2659T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208798 | ||||||
chr22:29208902
|
C | T | 1 | a0001c0002t0002g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.101+2763C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208902 | ||||||
chr22:29208983
|
C | T | 1 | a0002c0001t0001g0165 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.101+2844C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29208983 | ||||||
chr22:29209055
|
C | T | 1 | a0004c0004t0003g0209 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.101+2916C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209055 | ||||||
chr22:29209115
|
G | A | 1 | a0002c0001t0002g0011 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.101+2976G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209115 | ||||||
chr22:29209129
|
T | C | 4 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0001t0002g0021others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.101+2990T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209129 | ||||||
chr22:29209146
|
A | G | 1 | a0002c0001t0001g0164 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.101+3007A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209146 | ||||||
chr22:29209234
|
G | A | 1 | a0002c0001t0001g0039 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.101+3095G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209234 | ||||||
chr22:29209582
|
G | A | 24 | a0001c0002t0001g0229a0001c0002t0001g0234a0001c0002t0002g0186others(21): Show | 24 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.101+3443G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209582 | ||||||
chr22:29209633
|
A | G | 1 | a0001c0002t0002g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.101+3494A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209633 | ||||||
chr22:29209689
|
C | T | 1 | a0001c0002t0002g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.101+3550C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209689 | ||||||
chr22:29209735
|
A | G | 14 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(11): Show | 14 | HG01081.hp1 HG01255.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.101+3596A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209735 | ||||||
chr22:29209818
|
A | G | 4 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0002g0035others(1): Show | 4 | HG02723.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+3679A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209818 | ||||||
chr22:29209962
|
G | A | 1 | a0003c0003t0002g0040 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.101+3823G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29209962 | ||||||
chr22:29210168
|
C | G | 4 | a0003c0003t0001g0318a0003c0003t0001g0319a0003c0003t0001g0320others(1): Show | 4 | HG01496.hp1 HG02055.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.101+4029C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210168 | ||||||
chr22:29210168
|
C | T | 10 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(7): Show | 10 | HG01081.hp1 HG01255.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.101+4029C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210168 | ||||||
chr22:29210250
|
AT | A | 221 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0060others(218): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.101+4131delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 29210250 | |||||
chr22:29210254
|
T | C | 8 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(5): Show | 8 | HG01081.hp1 HG01255.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.101+4115T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210254 | ||||||
chr22:29210456
|
G | A | 1 | a0004c0004t0001g0213 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.101+4317G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210456 | ||||||
chr22:29210483
|
G | C | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.101+4344G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210483 | ||||||
chr22:29210593
|
C | T | 12 | a0001c0002t0001g0229a0001c0002t0002g0227a0001c0002t0002g0228others(9): Show | 12 | HG01074.hp1 HG01993.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.102-4333C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210593 | ||||||
chr22:29210877
|
G | A | 152 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0060others(149): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.102-4049G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210877 | ||||||
chr22:29210918
|
C | T | 19 | a0001c0002t0001g0234a0001c0002t0002g0186a0001c0002t0002g0219others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.102-4008C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29210918 | ||||||
chr22:29210957
|
A | AGT | 18 | a0001c0002t0001g0315a0001c0002t0002g0147a0001c0002t0002g0317others(15): Show | 18 | HG00639.hp2 HG01109.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.102-3956_102-3955d others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 29210957 | |||||
chr22:29211346
|
C | T | 5 | a0001c0002t0004g0001a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 6 | HG02109.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-3580C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211346 | ||||||
chr22:29211381
|
G | C | 1 | a0001c0002t0001g0236 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.102-3545G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211381 | ||||||
chr22:29211418
|
C | T | 197 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0060others(194): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.102-3508C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211418 | ||||||
chr22:29211467
|
C | T | 3 | a0001c0002t0001g0236a0002c0001t0001g0275a0002c0001t0001g0276 | 3 | HG02738.hp2 HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.102-3459C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211467 | ||||||
chr22:29211480
|
T | A | 12 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.102-3446T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211480 | ||||||
chr22:29211550
|
T | G | 2 | a0002c0001t0001g0041a0002c0001t0001g0164 | 2 | HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.102-3376T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211550 | ||||||
chr22:29211576
|
A | G | 1 | a0004c0004t0002g0145 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.102-3350A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211576 | ||||||
chr22:29211727
|
A | G | 1 | a0002c0001t0002g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.102-3199A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211727 | ||||||
chr22:29211938
|
TA | T | 24 | a0001c0002t0001g0297a0001c0002t0001g0300a0001c0002t0001g0301others(21): Show | 24 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.102-2987delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29211938 | ||||||
chr22:29212267
|
G | A | 17 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(14): Show | 18 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.102-2659G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212267 | ||||||
chr22:29212287
|
C | T | 243 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(240): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.102-2639C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212287 | ||||||
chr22:29212307
|
A | T | 1 | a0002c0001t0001g0010 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.102-2619A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212307 | ||||||
chr22:29212335
|
G | A | 242 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(239): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.102-2591G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212335 | ||||||
chr22:29212409
|
C | T | 1 | a0002c0001t0001g0274 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.102-2517C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212409 | ||||||
chr22:29212569
|
C | CT | 16 | a0001c0002t0001g0340a0001c0002t0003g0142a0001c0002t0003g0343others(13): Show | 17 | HG00099.hp1 HG00733.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.102-2345dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr22 | 29212569 | |||||
chr22:29212626
|
C | T | 19 | a0001c0002t0001g0234a0001c0002t0002g0186a0001c0002t0002g0219others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.102-2300C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212626 | ||||||
chr22:29212627
|
G | A | 1 | a0001c0002t0002g0042 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.102-2299G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212627 | ||||||
chr22:29212757
|
G | C | 2 | a0001c0002t0002g0290a0001c0002t0002g0291 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.102-2169G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212757 | ||||||
chr22:29212779
|
G | C | 4 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0001t0002g0021others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.102-2147G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212779 | ||||||
chr22:29212939
|
C | T | 1 | a0001c0002t0002g0291 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.102-1987C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212939 | ||||||
chr22:29212940
|
G | A | 3 | a0002c0001t0001g0006a0002c0001t0001g0007a0002c0001t0001g0008 | 3 | HG01256.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.102-1986G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29212940 | ||||||
chr22:29213396
|
A | G | 1 | a0002c0001t0001g0140 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.102-1530A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29213396 | ||||||
chr22:29213488
|
A | G | 2 | a0001c0002t0002g0288a0001c0002t0002g0289 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.102-1438A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29213488 | ||||||
chr22:29213586
|
G | A | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.102-1340G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29213586 | ||||||
chr22:29213598
|
G | A | 1 | a0001c0002t0001g0237 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.102-1328G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29213598 | ||||||
chr22:29214037
|
C | T | 7 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(4): Show | 7 | HG01884.hp2 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-889C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214037 | ||||||
chr22:29214149
|
A | G | 243 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(240): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.102-777A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214149 | ||||||
chr22:29214150
|
C | T | 5 | a0001c0002t0004g0001a0001c0002t0004g0024a0001c0002t0004g0025others(2): Show | 6 | HG02109.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-776C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214150 | ||||||
chr22:29214179
|
G | A | 5 | a0001c0002t0002g0043a0001c0002t0002g0044a0001c0002t0002g0159others(2): Show | 5 | NA18944.hp1 NA18966.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-747G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214179 | ||||||
chr22:29214248
|
T | G | 1 | a0002c0001t0001g0163 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.102-678T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214248 | ||||||
chr22:29214333
|
A | G | 1 | a0002c0001t0001g0293 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.102-593A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214333 | ||||||
chr22:29214343
|
T | C | 337 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(334): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.102-583T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214343 | ||||||
chr22:29214411
|
A | G | 12 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.102-515A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214411 | ||||||
chr22:29214654
|
C | T | 1 | a0002c0001t0007g0138 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.102-272C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 1/14 | chr22 | 29214654 | ||||||
chr22:29215247
|
T | C | 3 | a0001c0002t0001g0315a0001c0002t0002g0317a0001c0002t0003g0316 | 3 | HG02145.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.215+208T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 2/14 | chr22 | 29215247 | ||||||
chr22:29215360
|
G | T | 2 | a0001c0002t0002g0290a0001c0002t0002g0291 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.216-167G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 2/14 | chr22 | 29215360 | ||||||
chr22:29215876
|
A | G | 2 | a0001c0002t0001g0211a0001c0002t0001g0212 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.319+246A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29215876 | ||||||
chr22:29215917
|
G | T | 17 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(14): Show | 17 | HG00741.hp1 HG01081.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.319+287G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29215917 | ||||||
chr22:29215979
|
C | T | 16 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(13): Show | 16 | HG01070.hp2 HG01081.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.319+349C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29215979 | ||||||
chr22:29216051
|
C | T | 1 | a0002c0001t0001g0265 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.319+421C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216051 | ||||||
chr22:29216321
|
A | G | 2 | a0002c0001t0001g0135a0002c0001t0001g0136 | 2 | HG00544.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.319+691A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216321 | ||||||
chr22:29216331
|
C | T | 1 | a0002c0001t0001g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.319+701C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216331 | ||||||
chr22:29216473
|
G | C | 14 | a0001c0002t0001g0315a0001c0002t0002g0012a0001c0002t0002g0317others(11): Show | 14 | HG01346.hp1 HG01496.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.319+843G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216473 | ||||||
chr22:29216484
|
G | A | 6 | a0003c0003t0002g0325a0003c0003t0005g0282a0003c0003t0005g0283others(3): Show | 6 | HG02145.hp2 HG03041.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.319+854G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216484 | ||||||
chr22:29216492
|
G | A | 157 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0060others(154): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.319+862G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216492 | ||||||
chr22:29216514
|
A | C | 1 | a0001c0002t0002g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.319+884A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216514 | ||||||
chr22:29216519
|
A | G | 50 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0001g0188others(47): Show | 51 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.319+889A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216519 | ||||||
chr22:29216579
|
G | A | 2 | a0001c0002t0001g0238a0001c0002t0001g0239 | 2 | HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.319+949G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216579 | ||||||
chr22:29216714
|
C | T | 1 | a0001c0002t0006g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.319+1084C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216714 | ||||||
chr22:29216747
|
G | A | 339 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(336): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.319+1117G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216747 | ||||||
chr22:29216912
|
G | A | 1 | a0002c0001t0001g0284 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.319+1282G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216912 | ||||||
chr22:29216945
|
G | A | 25 | a0001c0002t0001g0117a0001c0002t0001g0234a0001c0002t0002g0219others(22): Show | 26 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.319+1315G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216945 | ||||||
chr22:29216959
|
C | G | 3 | a0001c0009t0001g0281a0002c0001t0001g0294a0002c0001t0002g0295 | 3 | HG02622.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.319+1329C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29216959 | ||||||
chr22:29217012
|
G | A | 7 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(4): Show | 7 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+1382G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217012 | ||||||
chr22:29217108
|
G | A | 1 | a0002c0001t0002g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.319+1478G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217108 | ||||||
chr22:29217379
|
G | A | 16 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(13): Show | 16 | HG01884.hp2 HG01891.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.319+1749G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217379 | ||||||
chr22:29217386
|
T | A | 4 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0002g0035others(1): Show | 4 | HG02723.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.319+1756T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217386 | ||||||
chr22:29217450
|
C | T | 36 | a0001c0002t0001g0124a0001c0002t0001g0236a0001c0002t0001g0237others(33): Show | 36 | HG00423.hp2 HG01515.hp2 HG02015.hp1 others(33): Show |
intron_variant | MODIFIER | c.319+1820C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217450 | ||||||
chr22:29217452
|
G | T | 66 | a0001c0002t0001g0124a0001c0002t0001g0211a0001c0002t0001g0212others(63): Show | 67 | HG00423.hp2 HG01346.hp1 HG01496.hp1 others(64): Show |
intron_variant | MODIFIER | c.319+1822G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217452 | ||||||
chr22:29217462
|
G | A | 9 | a0001c0002t0001g0211a0001c0002t0001g0212a0002c0001t0003g0336others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.319+1832G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217462 | ||||||
chr22:29217531
|
A | C | 342 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(339): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.319+1901A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217531 | ||||||
chr22:29217606
|
G | A | 1 | a0002c0001t0001g0244 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.319+1976G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217606 | ||||||
chr22:29217878
|
C | G | 1 | a0001c0002t0001g0116 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.319+2248C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217878 | ||||||
chr22:29217941
|
A | G | 64 | a0001c0002t0001g0030a0001c0002t0001g0117a0001c0002t0001g0173others(61): Show | 67 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.319+2311A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217941 | ||||||
chr22:29217965
|
T | C | 9 | a0001c0002t0001g0300a0002c0001t0001g0006a0002c0001t0001g0007others(6): Show | 9 | HG01081.hp2 HG01109.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.319+2335T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29217965 | ||||||
chr22:29218001
|
G | A | 15 | a0001c0002t0001g0300a0001c0002t0001g0301a0001c0002t0001g0302others(12): Show | 15 | HG01081.hp2 HG01109.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.319+2371G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218001 | ||||||
chr22:29218054
|
TCTC | T | 10 | a0001c0002t0001g0315a0001c0002t0002g0012a0001c0002t0002g0317others(7): Show | 10 | HG01346.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.319+2428_319+2430d others(5): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29218054 | |||||
chr22:29218111
|
C | T | 1 | a0002c0001t0002g0286 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.319+2481C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218111 | ||||||
chr22:29218195
|
G | A | 1 | a0001c0002t0002g0242 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.319+2565G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218195 | ||||||
chr22:29218205
|
G | A | 1 | a0001c0008t0002g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.319+2575G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218205 | ||||||
chr22:29218314
|
C | T | 15 | a0001c0002t0001g0211a0001c0002t0001g0212a0001c0002t0001g0340others(12): Show | 16 | HG00099.hp1 HG01099.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.319+2684C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218314 | ||||||
chr22:29218362
|
C | G | 10 | a0001c0002t0002g0197a0001c0002t0002g0199a0001c0002t0002g0200others(7): Show | 10 | HG01496.hp2 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.319+2732C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218362 | ||||||
chr22:29218577
|
A | G | 7 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0002g0032others(4): Show | 7 | HG02486.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+2947A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218577 | ||||||
chr22:29218601
|
A | G | 1 | a0001c0002t0002g0271 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.319+2971A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218601 | ||||||
chr22:29218688
|
C | T | 2 | a0002c0001t0002g0299a0002c0001t0002g0308 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.319+3058C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218688 | ||||||
chr22:29218689
|
G | A | 145 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0060others(142): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.319+3059G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218689 | ||||||
chr22:29218775
|
T | A | 2 | a0001c0002t0001g0326a0002c0001t0001g0327 | 2 | NA18942.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.319+3145T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218775 | ||||||
chr22:29218940
|
T | C | 32 | a0001c0002t0001g0030a0001c0002t0001g0173a0001c0002t0001g0175others(29): Show | 33 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.319+3310T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29218940 | ||||||
chr22:29219059
|
A | G | 1 | a0002c0001t0001g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.319+3429A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219059 | ||||||
chr22:29219268
|
C | G | 1 | a0001c0002t0002g0034 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.319+3638C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219268 | ||||||
chr22:29219306
|
G | A | 6 | a0001c0002t0004g0001a0001c0002t0004g0024a0001c0002t0004g0025others(3): Show | 7 | HG02109.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.319+3676G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219306 | ||||||
chr22:29219375
|
C | T | 14 | a0001c0002t0001g0315a0001c0002t0002g0012a0001c0002t0002g0317others(11): Show | 14 | HG01346.hp1 HG01496.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.319+3745C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219375 | ||||||
chr22:29219377
|
C | T | 1 | a0001c0002t0004g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.319+3747C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219377 | ||||||
chr22:29219547
|
A | C | 6 | a0001c0002t0001g0340a0001c0002t0003g0343a0002c0001t0001g0005others(3): Show | 7 | HG00099.hp1 HG01099.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+3917A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219547 | ||||||
chr22:29219613
|
C | CA | 10 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0002g0032others(7): Show | 10 | HG00639.hp1 HG01175.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.319+3993dupA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29219613 | |||||
chr22:29219743
|
C | T | 179 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0060others(176): Show | 181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.319+4113C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219743 | ||||||
chr22:29219801
|
T | G | 4 | a0003c0003t0001g0028a0003c0003t0001g0318a0003c0003t0001g0319others(1): Show | 4 | HG01496.hp1 HG02055.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+4171T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219801 | ||||||
chr22:29219824
|
C | G | 3 | a0001c0002t0001g0315a0001c0002t0002g0317a0001c0002t0003g0316 | 3 | HG02145.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.319+4194C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29219824 | ||||||
chr22:29220025
|
A | G | 29 | a0001c0002t0001g0285a0001c0002t0001g0297a0001c0002t0001g0300others(26): Show | 30 | HG01081.hp2 HG01109.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.319+4395A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220025 | ||||||
chr22:29220037
|
C | G | 7 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(4): Show | 7 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+4407C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220037 | ||||||
chr22:29220188
|
G | A | 1 | a0002c0001t0001g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.319+4558G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220188 | ||||||
chr22:29220276
|
A | G | 185 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0052others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.319+4646A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220276 | ||||||
chr22:29220287
|
C | T | 8 | a0001c0002t0002g0012a0002c0001t0001g0133a0002c0001t0003g0002others(5): Show | 9 | HG01346.hp1 NA18955.hp1 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.319+4657C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220287 | ||||||
chr22:29220744
|
A | C | 3 | a0001c0002t0001g0315a0001c0002t0002g0317a0001c0002t0003g0316 | 3 | HG02145.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.320-4389A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220744 | ||||||
chr22:29220759
|
C | T | 1 | a0002c0001t0001g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.320-4374C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220759 | ||||||
chr22:29220957
|
G | A | 6 | a0001c0002t0001g0301a0001c0002t0001g0302a0001c0002t0001g0305others(3): Show | 6 | HG01243.hp2 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.320-4176G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220957 | ||||||
chr22:29220994
|
T | G | 8 | a0001c0002t0002g0031a0001c0002t0002g0242a0001c0002t0004g0001others(5): Show | 9 | HG02109.hp2 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.320-4139T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29220994 | ||||||
chr22:29221053
|
C | G | 1 | a0001c0002t0002g0192 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.320-4080C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29221053 | ||||||
chr22:29221066
|
C | CGT | 8 | a0001c0002t0004g0025a0001c0002t0004g0026a0001c0002t0004g0027others(5): Show | 8 | HG02109.hp2 HG02572.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.320-4010_320-4009d others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221066
|
C | CGTGT | 9 | a0001c0002t0001g0300a0001c0002t0002g0271a0002c0001t0001g0312others(6): Show | 9 | HG02145.hp2 HG02258.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.320-4012_320-4009d others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221066
|
CGT | C | 20 | a0001c0002t0001g0269a0001c0002t0002g0105a0001c0002t0003g0046others(17): Show | 21 | HG00609.hp2 HG01243.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.320-4010_320-4009d others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221066
|
CGTGT | C | 30 | a0001c0002t0001g0091a0001c0002t0001g0093a0001c0002t0001g0097others(27): Show | 30 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.320-4012_320-4009d others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221066
|
CGTGTGT | C | 50 | a0001c0002t0001g0239a0001c0002t0001g0315a0001c0002t0002g0012others(47): Show | 50 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.320-4014_320-4009d others(8): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221066
|
CGTGTGTG others(1): Show |
C | 25 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0063others(22): Show | 25 | HG00558.hp2 HG00597.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.320-4016_320-4009d others(10): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221066
|
CGTGTGTG others(3): Show |
C | 30 | a0001c0002t0001g0052a0001c0002t0001g0301a0001c0002t0001g0302others(27): Show | 30 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.320-4018_320-4009d others(12): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221066
|
CGTGTGTG others(5): Show |
C | 2 | a0002c0001t0002g0051a0003c0003t0003g0292 | 2 | HG01517.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.320-4020_320-4009d others(14): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221066
|
CGTGTGTG others(9): Show |
C | 11 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0001g0188others(8): Show | 11 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.320-4024_320-4009d others(18): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221066
|
CGTGTGTG others(11): Show |
C | 34 | a0001c0002t0001g0173a0001c0002t0001g0175a0001c0002t0001g0178others(31): Show | 35 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.320-4026_320-4009d others(20): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221066
|
CGTGTGTG others(13): Show |
C | 54 | a0001c0002t0001g0116a0001c0002t0001g0124a0001c0002t0001g0143others(51): Show | 56 | HG00423.hp2 HG01070.hp2 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.320-4028_320-4009d others(22): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221066
|
CGTGTGTG others(15): Show |
C | 42 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(39): Show | 43 | HG00558.hp1 HG00733.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.320-4030_320-4009d others(24): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221066
|
CGTGTGTG others(17): Show |
C | 12 | a0001c0002t0001g0234a0001c0002t0002g0219a0001c0002t0002g0332others(9): Show | 12 | HG00280.hp2 HG00639.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.320-4032_320-4009d others(26): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221066
|
CGTGTGTG others(19): Show |
C | 1 | a0002c0001t0003g0339 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.320-4034_320-4009d others(28): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221066
|
CGTGTGTG others(21): Show |
C | 1 | a0003c0003t0001g0226 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.320-4036_320-4009d others(30): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221066 | |||||
chr22:29221132
|
G | T | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.320-4001G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29221132 | ||||||
chr22:29221249
|
GGGA | G | 140 | a0001c0002t0001g0052a0001c0002t0001g0059a0001c0002t0001g0060others(137): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.320-3879_320-3877d others(5): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29221249 | |||||
chr22:29221331
|
A | G | 89 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(86): Show | 92 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.320-3802A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29221331 | ||||||
chr22:29221500
|
G | A | 1 | a0001c0002t0002g0174 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.320-3633G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29221500 | ||||||
chr22:29221756
|
G | A | 1 | a0003c0003t0003g0168 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.320-3377G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29221756 | ||||||
chr22:29221963
|
A | T | 1 | a0003c0003t0003g0292 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.320-3170A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29221963 | ||||||
chr22:29222011
|
G | A | 339 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(336): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.320-3122G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222011 | ||||||
chr22:29222043
|
A | G | 6 | a0001c0002t0001g0326a0001c0002t0001g0331a0001c0002t0002g0330others(3): Show | 6 | HG00280.hp1 HG02698.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-3090A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222043 | ||||||
chr22:29222118
|
T | A | 7 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0002g0032others(4): Show | 7 | HG02486.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.320-3015T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222118 | ||||||
chr22:29222204
|
C | T | 2 | a0001c0002t0001g0211a0001c0002t0001g0212 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.320-2929C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222204 | ||||||
chr22:29222237
|
G | A | 7 | a0001c0002t0002g0031a0001c0002t0002g0242a0001c0002t0004g0001others(4): Show | 8 | HG02109.hp2 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.320-2896G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222237 | ||||||
chr22:29222329
|
A | G | 1 | a0001c0002t0002g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.320-2804A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222329 | ||||||
chr22:29222386
|
G | T | 6 | a0001c0002t0001g0340a0001c0002t0003g0343a0002c0001t0001g0005others(3): Show | 7 | HG00099.hp1 HG01099.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.320-2747G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222386 | ||||||
chr22:29222406
|
CT | C | 284 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(281): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.320-2708delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29222406 | |||||
chr22:29222406
|
CTT | C | 42 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0001g0117others(39): Show | 43 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.320-2709_320-2708d others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29222406 | |||||
chr22:29222524
|
C | G | 32 | a0001c0002t0001g0116a0001c0002t0001g0173a0001c0002t0001g0175others(29): Show | 33 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.320-2609C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222524 | ||||||
chr22:29222595
|
G | A | 2 | a0001c0002t0001g0211a0001c0002t0001g0212 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.320-2538G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222595 | ||||||
chr22:29222610
|
G | T | 1 | a0003c0003t0003g0088 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.320-2523G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222610 | ||||||
chr22:29222656
|
G | A | 3 | a0001c0002t0001g0108a0003c0003t0002g0040a0003c0003t0003g0058 | 3 | NA18954.hp2 NA19081.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.320-2477G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222656 | ||||||
chr22:29222916
|
C | G | 1 | a0001c0002t0002g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.320-2217C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29222916 | ||||||
chr22:29223009
|
T | C | 22 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(19): Show | 22 | HG01070.hp2 HG01081.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.320-2124T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223009 | ||||||
chr22:29223016
|
A | G | 2 | a0002c0001t0001g0056a0004c0004t0001g0057 | 2 | HG01261.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.320-2117A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223016 | ||||||
chr22:29223022
|
C | T | 2 | a0002c0001t0001g0294a0002c0001t0002g0295 | 2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.320-2111C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223022 | ||||||
chr22:29223028
|
T | C | 12 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(9): Show | 12 | HG01884.hp2 HG02145.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.320-2105T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223028 | ||||||
chr22:29223047
|
C | T | 26 | a0001c0002t0001g0117a0001c0002t0001g0234a0001c0002t0002g0219others(23): Show | 27 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.320-2086C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223047 | ||||||
chr22:29223476
|
G | C | 2 | a0002c0001t0002g0299a0002c0001t0002g0308 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.320-1657G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223476 | ||||||
chr22:29223600
|
T | C | 1 | a0001c0002t0001g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.320-1533T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223600 | ||||||
chr22:29223604
|
A | C | 26 | a0001c0002t0001g0117a0001c0002t0001g0234a0001c0002t0002g0219others(23): Show | 27 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.320-1529A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223604 | ||||||
chr22:29223745
|
A | AG | 7 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0002g0035others(4): Show | 7 | HG02258.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.320-1387dupG | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr22 | 29223745 | |||||
chr22:29223778
|
C | A | 1 | a0001c0002t0002g0201 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.320-1355C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29223778 | ||||||
chr22:29224079
|
C | T | 2 | a0002c0001t0002g0106a0002c0001t0003g0107 | 2 | NA18939.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.320-1054C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224079 | ||||||
chr22:29224135
|
G | C | 1 | a0001c0002t0003g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.320-998G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224135 | ||||||
chr22:29224186
|
C | T | 1 | a0002c0001t0002g0280 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.320-947C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224186 | ||||||
chr22:29224187
|
G | A | 30 | a0001c0002t0001g0124a0001c0002t0001g0236a0001c0002t0001g0237others(27): Show | 30 | HG00423.hp2 HG01515.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.320-946G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224187 | ||||||
chr22:29224243
|
C | T | 155 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0063others(152): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.320-890C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224243 | ||||||
chr22:29224316
|
C | T | 3 | a0001c0002t0002g0223a0003c0003t0003g0224a0004c0004t0001g0213 | 3 | HG00733.hp1 HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.320-817C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224316 | ||||||
chr22:29224336
|
A | C | 79 | a0001c0002t0001g0019a0001c0002t0001g0117a0001c0002t0001g0124others(76): Show | 81 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.320-797A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224336 | ||||||
chr22:29224396
|
C | T | 2 | a0001c0002t0001g0137a0001c0002t0001g0143 | 2 | NA18943.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.320-737C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224396 | ||||||
chr22:29224469
|
G | C | 6 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(3): Show | 6 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-664G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224469 | ||||||
chr22:29224472
|
T | C | 29 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(26): Show | 30 | HG01070.hp2 HG01081.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.320-661T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224472 | ||||||
chr22:29224499
|
G | T | 1 | a0001c0002t0002g0242 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320-634G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224499 | ||||||
chr22:29224573
|
T | A | 38 | a0001c0002t0001g0091a0001c0002t0001g0173a0001c0002t0001g0175others(35): Show | 40 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.320-560T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224573 | ||||||
chr22:29224575
|
A | G | 332 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(329): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.320-558A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224575 | ||||||
chr22:29224625
|
C | T | 1 | a0002c0001t0007g0161 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.320-508C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224625 | ||||||
chr22:29224690
|
G | C | 1 | a0001c0002t0002g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.320-443G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224690 | ||||||
chr22:29224911
|
C | T | 7 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.320-222C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224911 | ||||||
chr22:29224913
|
C | T | 1 | a0001c0002t0002g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.320-220C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29224913 | ||||||
chr22:29225072
|
CA | C | 21 | a0001c0002t0001g0014a0001c0002t0001g0234a0001c0002t0001g0238others(18): Show | 21 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.320-60delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29225072 | ||||||
chr22:29225079
|
G | A | 1 | a0002c0001t0001g0092 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.320-54G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 3/14 | chr22 | 29225079 | ||||||
chr22:29225414
|
C | T | 1 | a0001c0002t0002g0159 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.403+198C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29225414 | ||||||
chr22:29225488
|
C | T | 336 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(333): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.403+272C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29225488 | ||||||
chr22:29225594
|
G | T | 1 | a0002c0001t0008g0263 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.403+378G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29225594 | ||||||
chr22:29225656
|
G | A | 2 | a0002c0001t0002g0021a0002c0001t0002g0022 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.403+440G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29225656 | ||||||
chr22:29225872
|
T | C | 337 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(334): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.404-618T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29225872 | ||||||
chr22:29225911
|
G | A | 1 | a0002c0001t0002g0106 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.404-579G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29225911 | ||||||
chr22:29225999
|
C | T | 1 | a0001c0002t0004g0026 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.404-491C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29225999 | ||||||
chr22:29226000
|
G | A | 24 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(21): Show | 24 | HG01346.hp1 HG01891.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.404-490G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226000 | ||||||
chr22:29226019
|
C | A | 1 | a0001c0002t0001g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.404-471C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226019 | ||||||
chr22:29226139
|
G | A | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.404-351G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226139 | ||||||
chr22:29226175
|
C | T | 2 | a0001c0002t0002g0191a0001c0002t0002g0277 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.404-315C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226175 | ||||||
chr22:29226178
|
C | A | 1 | a0004c0004t0003g0071 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.404-312C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226178 | ||||||
chr22:29226178
|
C | T | 4 | a0003c0003t0001g0028a0003c0003t0001g0318a0003c0003t0001g0319others(1): Show | 4 | HG01496.hp1 HG02055.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-312C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226178 | ||||||
chr22:29226265
|
G | C | 15 | a0001c0002t0001g0285a0001c0002t0002g0191a0001c0002t0002g0197others(12): Show | 15 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.404-225G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226265 | ||||||
chr22:29226322
|
C | T | 3 | a0001c0002t0002g0193a0001c0002t0002g0194a0001c0002t0002g0195 | 3 | NA18955.hp2 NA19005.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.404-168C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226322 | ||||||
chr22:29226387
|
A | G | 16 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(13): Show | 17 | HG01496.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-103A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226387 | ||||||
chr22:29226415
|
C | T | 1 | a0001c0002t0002g0182 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.404-75C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 4/14 | chr22 | 29226415 | ||||||
chr22:29226647
|
A | G | 23 | a0001c0002t0001g0019a0001c0002t0001g0036a0001c0002t0001g0037others(20): Show | 23 | HG01081.hp2 HG01109.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.465+96A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29226647 | ||||||
chr22:29226674
|
G | A | 3 | a0002c0001t0001g0169a0002c0001t0001g0170a0002c0001t0001g0171 | 3 | NA18947.hp2 NA19011.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.465+123G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29226674 | ||||||
chr22:29226716
|
C | T | 2 | a0002c0001t0001g0068a0002c0001t0001g0089 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.465+165C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29226716 | ||||||
chr22:29226833
|
G | T | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.465+282G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29226833 | ||||||
chr22:29226941
|
C | T | 15 | a0001c0002t0001g0285a0001c0002t0002g0191a0001c0002t0002g0197others(12): Show | 15 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.465+390C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29226941 | ||||||
chr22:29226988
|
T | A | 183 | a0001c0002t0001g0019a0001c0002t0001g0030a0001c0002t0001g0036others(180): Show | 184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.465+437T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29226988 | ||||||
chr22:29227000
|
C | A | 14 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(11): Show | 15 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.465+449C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227000 | ||||||
chr22:29227045
|
A | T | 1 | a0001c0002t0002g0258 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.465+494A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227045 | ||||||
chr22:29227394
|
C | CTT | 15 | a0001c0002t0001g0285a0001c0002t0002g0191a0001c0002t0002g0197others(12): Show | 15 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.465+856_465+857dup others(2): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29227394 | |||||
chr22:29227409
|
A | G | 1 | a0001c0002t0003g0343 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.465+858A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227409 | ||||||
chr22:29227414
|
A | G | 1 | a0001c0008t0002g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.465+863A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227414 | ||||||
chr22:29227436
|
G | A | 1 | a0001c0002t0003g0259 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.465+885G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227436 | ||||||
chr22:29227449
|
A | G | 13 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0091others(10): Show | 13 | HG00558.hp1 HG00609.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.465+898A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227449 | ||||||
chr22:29227478
|
G | A | 1 | a0003c0003t0001g0320 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.465+927G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227478 | ||||||
chr22:29227704
|
C | CA | 7 | a0001c0002t0002g0072a0001c0002t0002g0160a0002c0001t0001g0155others(4): Show | 7 | HG00544.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.465+1176dupA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29227704 | |||||
chr22:29227704
|
CA | C | 52 | a0001c0002t0001g0019a0001c0002t0001g0030a0001c0002t0001g0052others(49): Show | 54 | HG00099.hp1 HG00280.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.465+1176delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29227704 | |||||
chr22:29227704
|
CAA | C | 86 | a0001c0002t0001g0190a0001c0002t0001g0211a0001c0002t0001g0212others(83): Show | 87 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.465+1175_465+1176d others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29227704 | |||||
chr22:29227704
|
CAAA | C | 22 | a0001c0002t0001g0018a0001c0002t0001g0117a0002c0001t0001g0023others(19): Show | 22 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.465+1174_465+1176d others(5): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29227704 | |||||
chr22:29227725
|
A | AAC | 7 | a0001c0002t0001g0091a0001c0002t0001g0108a0001c0002t0002g0013others(4): Show | 7 | HG00558.hp1 HG00609.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.465+1175_465+1176i others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29227725 | |||||
chr22:29227725
|
A | AC | 37 | a0001c0002t0001g0014a0001c0002t0001g0036a0001c0002t0001g0037others(34): Show | 38 | HG01346.hp1 HG01891.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.465+1174_465+1175i others(3): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227725 | ||||||
chr22:29227725
|
A | C | 117 | a0001c0002t0001g0019a0001c0002t0001g0052a0001c0002t0001g0060others(114): Show | 119 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.465+1174A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227725 | ||||||
chr22:29227782
|
G | A | 1 | a0003c0003t0003g0208 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.465+1231G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227782 | ||||||
chr22:29227786
|
C | T | 1 | a0001c0002t0002g0195 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.465+1235C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227786 | ||||||
chr22:29227839
|
C | A | 3 | a0003c0003t0001g0333a0003c0003t0001g0334a0003c0003t0001g0335 | 3 | HG02258.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.465+1288C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227839 | ||||||
chr22:29227859
|
C | G | 5 | a0001c0002t0002g0032a0001c0002t0002g0034a0003c0003t0001g0333others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+1308C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227859 | ||||||
chr22:29227871
|
C | T | 4 | a0001c0002t0002g0076a0001c0002t0002g0077a0001c0002t0002g0160others(1): Show | 4 | HG00408.hp1 HG00438.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+1320C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227871 | ||||||
chr22:29227930
|
C | T | 3 | a0001c0002t0001g0255a0001c0002t0001g0256a0002c0001t0001g0257 | 3 | HG02683.hp2 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.465+1379C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227930 | ||||||
chr22:29227931
|
G | A | 1 | a0003c0003t0003g0292 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.465+1380G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227931 | ||||||
chr22:29227970
|
A | G | 2 | a0001c0002t0002g0197a0002c0001t0001g0029 | 2 | HG01496.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.465+1419A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227970 | ||||||
chr22:29227994
|
A | G | 106 | a0001c0002t0001g0014a0001c0002t0001g0019a0001c0002t0001g0036others(103): Show | 108 | HG00280.hp1 HG00558.hp1 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.465+1443A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29227994 | ||||||
chr22:29228051
|
G | A | 20 | a0001c0002t0001g0229a0001c0002t0001g0285a0001c0002t0002g0191others(17): Show | 21 | HG00099.hp1 HG01074.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.465+1500G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228051 | ||||||
chr22:29228104
|
C | T | 1 | a0003c0003t0001g0210 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.465+1553C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228104 | ||||||
chr22:29228150
|
C | T | 3 | a0001c0002t0003g0003a0001c0002t0003g0214a0002c0001t0003g0232 | 4 | NA18747.hp1 NA18964.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+1599C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228150 | ||||||
chr22:29228156
|
C | CA | 49 | a0001c0002t0001g0014a0001c0002t0001g0036a0001c0002t0001g0037others(46): Show | 51 | HG00558.hp1 HG00609.hp1 HG01192.hp1 others(48): Show |
intron_variant | MODIFIER | c.465+1626dupA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29228156 | |||||
chr22:29228156
|
C | CAA | 10 | a0001c0002t0001g0173a0001c0002t0001g0175a0001c0002t0002g0123others(7): Show | 10 | HG03017.hp2 HG03491.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.465+1625_465+1626d others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29228156 | |||||
chr22:29228156
|
CA | C | 13 | a0001c0002t0001g0305a0001c0002t0002g0258a0002c0001t0001g0078others(10): Show | 13 | HG00733.hp1 HG01070.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.465+1626delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29228156 | |||||
chr22:29228178
|
T | A | 1 | a0002c0001t0002g0295 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.465+1627T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228178 | ||||||
chr22:29228329
|
A | G | 2 | a0001c0002t0001g0124a0002c0001t0001g0341 | 2 | HG02148.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.465+1778A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228329 | ||||||
chr22:29228593
|
T | C | 45 | a0001c0002t0001g0014a0001c0002t0001g0036a0001c0002t0001g0037others(42): Show | 46 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.465+2042T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228593 | ||||||
chr22:29228856
|
G | A | 1 | a0001c0002t0001g0305 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.466-2164G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228856 | ||||||
chr22:29228892
|
A | T | 51 | a0001c0002t0001g0014a0001c0002t0001g0036a0001c0002t0001g0037others(48): Show | 52 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(49): Show |
intron_variant | MODIFIER | c.466-2128A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228892 | ||||||
chr22:29228898
|
G | A | 1 | a0002c0001t0001g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.466-2122G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29228898 | ||||||
chr22:29229077
|
C | T | 1 | a0001c0002t0001g0305 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.466-1943C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229077 | ||||||
chr22:29229278
|
G | A | 1 | a0001c0002t0003g0343 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.466-1742G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229278 | ||||||
chr22:29229310
|
G | T | 3 | a0003c0003t0003g0015a0003c0003t0003g0016a0004c0004t0003g0306 | 3 | HG02886.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.466-1710G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229310 | ||||||
chr22:29229318
|
G | A | 5 | a0001c0002t0001g0297a0002c0001t0001g0312a0002c0001t0003g0336others(2): Show | 5 | HG02257.hp1 HG02572.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-1702G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229318 | ||||||
chr22:29229369
|
C | T | 1 | a0001c0002t0002g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.466-1651C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229369 | ||||||
chr22:29229414
|
C | T | 1 | a0002c0001t0001g0023 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.466-1606C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229414 | ||||||
chr22:29229643
|
C | CA | 102 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0036others(99): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.466-1361dupA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29229643 | |||||
chr22:29229643
|
CA | C | 7 | a0001c0002t0002g0105a0002c0001t0001g0158a0003c0003t0003g0016others(4): Show | 7 | HG00639.hp1 HG01175.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.466-1361delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29229643 | |||||
chr22:29229657
|
A | G | 2 | a0001c0002t0002g0317a0001c0002t0003g0316 | 2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.466-1363A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229657 | ||||||
chr22:29229917
|
C | T | 1 | a0001c0002t0002g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.466-1103C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229917 | ||||||
chr22:29229922
|
G | A | 207 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(204): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.466-1098G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229922 | ||||||
chr22:29229957
|
T | C | 1 | a0002c0001t0001g0342 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.466-1063T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29229957 | ||||||
chr22:29230091
|
G | A | 1 | a0002c0001t0001g0039 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.466-929G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230091 | ||||||
chr22:29230201
|
C | T | 20 | a0001c0002t0001g0229a0001c0002t0001g0285a0001c0002t0002g0191others(17): Show | 21 | HG00099.hp1 HG01074.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.466-819C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230201 | ||||||
chr22:29230336
|
GA | G | 179 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(176): Show | 180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.466-672delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr22 | 29230336 | |||||
chr22:29230338
|
A | G | 87 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0036others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.466-682A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230338 | ||||||
chr22:29230342
|
A | C | 2 | a0001c0009t0001g0281a0002c0001t0002g0102 | 2 | NA19043.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.466-678A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230342 | ||||||
chr22:29230347
|
A | C | 5 | a0003c0003t0002g0085a0003c0003t0003g0067a0003c0003t0003g0084others(2): Show | 5 | NA18945.hp1 NA18947.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-673A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230347 | ||||||
chr22:29230348
|
A | C | 1 | a0003c0003t0002g0321 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.466-672A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230348 | ||||||
chr22:29230525
|
C | T | 1 | a0001c0002t0001g0305 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.466-495C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230525 | ||||||
chr22:29230526
|
G | A | 5 | a0001c0002t0001g0229a0002c0001t0001g0005a0002c0001t0001g0276others(2): Show | 6 | HG00099.hp1 HG01074.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-494G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230526 | ||||||
chr22:29230624
|
C | T | 207 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(204): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.466-396C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230624 | ||||||
chr22:29230794
|
A | T | 1 | a0001c0002t0003g0343 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.466-226A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230794 | ||||||
chr22:29230804
|
A | T | 54 | a0001c0002t0001g0030a0001c0002t0001g0305a0001c0002t0003g0343others(51): Show | 55 | HG00438.hp1 HG00639.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.466-216A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230804 | ||||||
chr22:29230813
|
A | G | 188 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(185): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.466-207A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230813 | ||||||
chr22:29230871
|
G | A | 50 | a0003c0003t0001g0028a0003c0003t0001g0210a0003c0003t0001g0226others(47): Show | 51 | HG00438.hp1 HG00639.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.466-149G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230871 | ||||||
chr22:29230885
|
G | A | 1 | a0001c0002t0003g0343 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.466-135G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230885 | ||||||
chr22:29230904
|
G | A | 1 | a0001c0002t0001g0305 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.466-116G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230904 | ||||||
chr22:29230926
|
G | A | 1 | a0001c0002t0001g0247 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.466-94G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29230926 | ||||||
chr22:29231000
|
G | A | 1 | a0001c0002t0001g0188 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.466-20G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 5/14 | chr22 | 29231000 | ||||||
chr22:29231298
|
C | T | 4 | a0003c0003t0002g0040a0003c0003t0003g0058a0003c0003t0003g0260others(1): Show | 4 | HG00438.hp1 HG02015.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+158C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231298 | ||||||
chr22:29231349
|
G | C | 2 | a0002c0001t0003g0217a0002c0001t0003g0241 | 2 | HG00280.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.586+209G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231349 | ||||||
chr22:29231441
|
T | A | 1 | a0001c0002t0001g0315 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.587-152T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231441 | ||||||
chr22:29231442
|
AC | A | 41 | a0001c0002t0001g0014a0001c0002t0001g0030a0001c0002t0001g0059others(38): Show | 41 | HG00558.hp1 HG00609.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.587-143delC | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr22 | 29231442 | |||||
chr22:29231448
|
C | T | 1 | a0001c0002t0003g0179 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.587-145C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231448 | ||||||
chr22:29231450
|
C | G | 4 | a0001c0002t0001g0030a0001c0002t0001g0305a0001c0002t0003g0343others(1): Show | 4 | HG01099.hp2 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-143C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231450 | ||||||
chr22:29231462
|
G | C | 3 | a0001c0002t0001g0255a0001c0002t0001g0256a0002c0001t0001g0257 | 3 | HG02683.hp2 HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.587-131G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231462 | ||||||
chr22:29231502
|
C | T | 1 | a0001c0002t0002g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.587-91C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231502 | ||||||
chr22:29231543
|
G | T | 2 | a0001c0002t0001g0305a0001c0009t0001g0281 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.587-50G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231543 | ||||||
chr22:29231547
|
C | G | 20 | a0001c0002t0001g0229a0001c0002t0001g0285a0001c0002t0002g0191others(17): Show | 21 | HG00099.hp1 HG01074.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.587-46C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231547 | ||||||
chr22:29231588
|
C | G | 5 | a0001c0002t0002g0032a0001c0002t0002g0034a0003c0003t0001g0333others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG03225.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.587-5C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 6/14 | chr22 | 29231588 | ||||||
chr22:29231888
|
C | A | 1 | a0002c0001t0001g0080 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.676+206C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 7/14 | chr22 | 29231888 | ||||||
chr22:29231955
|
C | G | 6 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(3): Show | 7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.676+273C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 7/14 | chr22 | 29231955 | ||||||
chr22:29232107
|
C | G | 137 | a0001c0002t0001g0063a0001c0002t0001g0093a0001c0002t0001g0097others(134): Show | 139 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.677-149C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 7/14 | chr22 | 29232107 | ||||||
chr22:29232195
|
A | G | 2 | a0001c0002t0001g0301a0001c0002t0001g0302 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.677-61A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 7/14 | chr22 | 29232195 | ||||||
chr22:29232233
|
A | G | 1 | a0001c0002t0001g0285 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.677-23A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 7/14 | chr22 | 29232233 | ||||||
chr22:29232542
|
C | T | 2 | a0002c0001t0002g0054a0002c0001t0002g0069 | 2 | HG03490.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.823+140C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29232542 | ||||||
chr22:29232626
|
G | A | 135 | a0001c0002t0001g0063a0001c0002t0001g0093a0001c0002t0001g0097others(132): Show | 137 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.823+224G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29232626 | ||||||
chr22:29232681
|
G | C | 5 | a0003c0003t0001g0028a0003c0003t0001g0318a0003c0003t0001g0319others(2): Show | 5 | HG01496.hp1 HG02055.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.823+279G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29232681 | ||||||
chr22:29232703
|
T | G | 1 | a0001c0002t0001g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.823+301T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29232703 | ||||||
chr22:29232752
|
C | T | 34 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0239others(31): Show | 34 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.823+350C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29232752 | ||||||
chr22:29232817
|
G | A | 56 | a0003c0003t0001g0028a0003c0003t0001g0210a0003c0003t0001g0226others(53): Show | 57 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.823+415G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29232817 | ||||||
chr22:29232909
|
TCTC | T | 8 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.824-468_824-466del others(3): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr22 | 29232909 | |||||
chr22:29233024
|
G | C | 4 | a0002c0001t0001g0078a0002c0001t0001g0080a0002c0001t0001g0140others(1): Show | 4 | HG00733.hp2 HG01070.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.824-355G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29233024 | ||||||
chr22:29233174
|
G | T | 1 | a0001c0002t0002g0317 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.824-205G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29233174 | ||||||
chr22:29233240
|
G | T | 2 | a0001c0002t0002g0258a0002c0001t0001g0254 | 2 | NA18959.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.824-139G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 8/14 | chr22 | 29233240 | ||||||
chr22:29233737
|
C | T | 9 | a0001c0002t0001g0313a0001c0002t0002g0125a0001c0002t0002g0126others(6): Show | 9 | NA18948.hp1 NA18959.hp1 NA18977.hp2 others(6): Show |
intron_variant | MODIFIER | c.966+71C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 10/14 | chr22 | 29233737 | ||||||
chr22:29234226
|
G | A | 1 | a0001c0002t0001g0300 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1029+27G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 11/14 | chr22 | 29234226 | ||||||
chr22:29234280
|
C | T | 1 | a0001c0002t0001g0340 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1030-25C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 11/14 | chr22 | 29234280 | ||||||
chr22:29234292
|
C | T | 1 | a0001c0002t0001g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1030-13C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 11/14 | chr22 | 29234292 | ||||||
chr22:29234360
|
C | T | 2 | a0003c0003t0001g0028a0003c0003t0001g0320 | 2 | HG01496.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1074+11C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29234360 | ||||||
chr22:29234509
|
T | C | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1074+160T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29234509 | ||||||
chr22:29234575
|
C | T | 299 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(296): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1074+226C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29234575 | ||||||
chr22:29234633
|
G | A | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1074+284G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29234633 | ||||||
chr22:29234833
|
C | G | 294 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(291): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1074+484C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29234833 | ||||||
chr22:29234902
|
A | G | 42 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(39): Show | 43 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1074+553A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29234902 | ||||||
chr22:29234995
|
G | A | 1 | a0001c0002t0002g0013 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1074+646G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29234995 | ||||||
chr22:29235046
|
A | T | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1074+697A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29235046 | ||||||
chr22:29235103
|
T | C | 67 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(64): Show | 70 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1074+754T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29235103 | ||||||
chr22:29235158
|
G | A | 1 | a0001c0002t0001g0108 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1074+809G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29235158 | ||||||
chr22:29235348
|
C | CA | 10 | a0001c0002t0001g0093a0001c0002t0002g0094a0001c0002t0002g0125others(7): Show | 10 | HG00741.hp2 HG01099.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1074+1019dupA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235348 | |||||
chr22:29235348
|
CA | C | 26 | a0001c0002t0001g0097a0001c0002t0001g0234a0001c0002t0001g0331others(23): Show | 26 | HG00099.hp2 HG00408.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1074+1019delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235348 | |||||
chr22:29235348
|
CAA | C | 89 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0239others(86): Show | 90 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1074+1018_1074+101 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235348 | |||||
chr22:29235348
|
CAAA | C | 62 | a0001c0002t0001g0014a0001c0002t0001g0030a0001c0002t0001g0059others(59): Show | 64 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1074+1017_1074+101 others(7): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235348 | |||||
chr22:29235616
|
A | G | 3 | a0001c0002t0002g0223a0002c0001t0001g0068a0002c0001t0001g0089 | 3 | HG01192.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1074+1267A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29235616 | ||||||
chr22:29235780
|
C | CT | 64 | a0001c0002t0001g0063a0001c0002t0001g0116a0001c0002t0001g0117others(61): Show | 64 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1074+1458dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235780 | |||||
chr22:29235780
|
C | CTT | 12 | a0001c0002t0001g0236a0001c0002t0002g0094a0001c0002t0002g0125others(9): Show | 12 | HG00741.hp2 HG02071.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.1074+1457_1074+145 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235780 | |||||
chr22:29235780
|
CT | C | 10 | a0001c0002t0001g0239a0001c0002t0001g0269a0001c0002t0001g0305others(7): Show | 10 | HG01167.hp2 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1074+1458delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235780 | |||||
chr22:29235780
|
CTT | C | 24 | a0001c0002t0001g0059a0001c0002t0001g0285a0001c0002t0002g0031others(21): Show | 25 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1074+1457_1074+145 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235780 | |||||
chr22:29235780
|
CTTT | C | 48 | a0001c0002t0001g0019a0001c0002t0001g0036a0001c0002t0001g0037others(45): Show | 49 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1074+1456_1074+145 others(7): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235780 | |||||
chr22:29235780
|
CTTTT | C | 20 | a0001c0002t0001g0014a0001c0002t0001g0173a0001c0002t0001g0175others(17): Show | 20 | HG00741.hp1 HG01081.hp2 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1074+1455_1074+145 others(8): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235780 | |||||
chr22:29235780
|
CTTTTT | C | 47 | a0003c0003t0001g0028a0003c0003t0001g0210a0003c0003t0001g0318others(44): Show | 48 | HG00438.hp1 HG00639.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.1074+1454_1074+145 others(9): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29235780 | |||||
chr22:29235793
|
T | C | 6 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(3): Show | 7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1074+1444T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29235793 | ||||||
chr22:29235814
|
G | T | 1 | a0001c0002t0006g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1074+1465G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29235814 | ||||||
chr22:29236063
|
A | T | 1 | a0002c0001t0001g0244 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1074+1714A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236063 | ||||||
chr22:29236122
|
A | G | 1 | a0001c0002t0001g0239 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1074+1773A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236122 | ||||||
chr22:29236269
|
A | C | 94 | a0001c0002t0001g0018a0001c0002t0001g0030a0001c0002t0001g0117others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1074+1920A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236269 | ||||||
chr22:29236407
|
T | C | 23 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0091others(20): Show | 24 | HG00558.hp1 HG00609.hp1 HG02080.hp1 others(21): Show |
intron_variant | MODIFIER | c.1074+2058T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236407 | ||||||
chr22:29236418
|
C | T | 35 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(32): Show | 35 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.1074+2069C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236418 | ||||||
chr22:29236465
|
G | T | 1 | a0001c0002t0001g0143 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1074+2116G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236465 | ||||||
chr22:29236506
|
C | T | 3 | a0003c0003t0001g0333a0003c0003t0001g0334a0003c0003t0001g0335 | 3 | HG02258.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1074+2157C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236506 | ||||||
chr22:29236519
|
C | T | 7 | a0001c0002t0001g0326a0001c0002t0001g0331a0001c0002t0002g0330others(4): Show | 7 | HG00280.hp1 HG02698.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.1074+2170C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236519 | ||||||
chr22:29236568
|
G | A | 200 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(197): Show | 204 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.1074+2219G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236568 | ||||||
chr22:29236607
|
C | T | 125 | a0001c0002t0001g0063a0001c0002t0001g0093a0001c0002t0001g0097others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1074+2258C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236607 | ||||||
chr22:29236742
|
T | C | 59 | a0003c0003t0001g0028a0003c0003t0001g0210a0003c0003t0001g0226others(56): Show | 60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1074+2393T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236742 | ||||||
chr22:29236749
|
A | G | 34 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0239others(31): Show | 34 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.1074+2400A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236749 | ||||||
chr22:29236798
|
T | C | 7 | a0001c0002t0001g0014a0001c0002t0001g0315a0001c0002t0002g0013others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074+2449T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236798 | ||||||
chr22:29236837
|
C | T | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1074+2488C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236837 | ||||||
chr22:29236883
|
G | A | 1 | a0002c0001t0001g0049 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1074+2534G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236883 | ||||||
chr22:29236893
|
A | T | 35 | a0001c0002t0001g0018a0001c0002t0001g0030a0001c0002t0001g0117others(32): Show | 35 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1074+2544A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29236893 | ||||||
chr22:29237040
|
C | T | 1 | a0003c0003t0003g0004 | 2 | NA18969.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1074+2691C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237040 | ||||||
chr22:29237041
|
G | A | 1 | a0002c0001t0001g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1074+2692G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237041 | ||||||
chr22:29237070
|
C | T | 94 | a0001c0002t0001g0018a0001c0002t0001g0030a0001c0002t0001g0117others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1074+2721C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237070 | ||||||
chr22:29237086
|
C | G | 93 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0239others(90): Show | 94 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1074+2737C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237086 | ||||||
chr22:29237097
|
TATTTTCT others(2297): Show |
T | 69 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(66): Show | 72 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1074+2752_1075-404 others(4): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29237097 | |||||
chr22:29237245
|
T | C | 93 | a0001c0002t0001g0018a0001c0002t0001g0030a0001c0002t0001g0117others(90): Show | 94 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1074+2896T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237245 | ||||||
chr22:29237378
|
A | G | 1 | a0002c0001t0003g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1074+3029A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237378 | ||||||
chr22:29237499
|
T | C | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1074+3150T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237499 | ||||||
chr22:29237615
|
G | A | 1 | a0001c0002t0001g0239 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1074+3266G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237615 | ||||||
chr22:29237800
|
C | CA | 127 | a0001c0002t0001g0063a0001c0002t0001g0093a0001c0002t0001g0097others(124): Show | 128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1074+3459dupA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29237800 | |||||
chr22:29237800
|
C | G | 23 | a0001c0002t0001g0019a0001c0002t0001g0036a0001c0002t0001g0037others(20): Show | 23 | HG01081.hp2 HG01109.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1074+3451C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237800 | ||||||
chr22:29237837
|
C | T | 94 | a0001c0002t0001g0018a0001c0002t0001g0030a0001c0002t0001g0117others(91): Show | 95 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1074+3488C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237837 | ||||||
chr22:29237907
|
C | T | 6 | a0001c0002t0003g0046a0001c0002t0003g0218a0001c0002t0003g0233others(3): Show | 6 | HG00280.hp2 HG02132.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+3558C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237907 | ||||||
chr22:29237946
|
G | A | 34 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0239others(31): Show | 34 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.1074+3597G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29237946 | ||||||
chr22:29238154
|
G | C | 1 | a0001c0002t0002g0317 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1074+3805G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238154 | ||||||
chr22:29238254
|
A | AATT | 10 | a0001c0002t0001g0036a0001c0002t0002g0077a0001c0002t0002g0258others(7): Show | 10 | HG00438.hp2 HG01515.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1074+3952_1074+395 others(7): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238254 | |||||
chr22:29238254
|
AATT | A | 55 | a0001c0002t0001g0030a0001c0002t0001g0117a0001c0002t0001g0137others(52): Show | 55 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1074+3952_1074+395 others(7): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238254 | |||||
chr22:29238254
|
AATTATT | A | 26 | a0001c0002t0001g0093a0001c0002t0001g0188a0001c0002t0001g0189others(23): Show | 26 | HG00642.hp2 HG01070.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.1074+3949_1074+395 others(10): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238254 | |||||
chr22:29238254
|
AATTATTA others(2): Show |
A | 50 | a0001c0002t0001g0018a0001c0002t0001g0234a0001c0002t0002g0186others(47): Show | 51 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1074+3946_1074+395 others(13): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238254 | |||||
chr22:29238254
|
AATTATTA others(5): Show |
A | 17 | a0001c0002t0001g0019a0001c0002t0002g0177a0001c0002t0003g0343others(14): Show | 17 | HG01081.hp2 HG01099.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1074+3943_1074+395 others(16): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238254 | |||||
chr22:29238254
|
AATTATTA others(8): Show |
A | 2 | a0001c0002t0001g0052a0001c0008t0002g0047 | 2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1074+3940_1074+395 others(19): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238254 | |||||
chr22:29238254
|
AATTATTA others(14): Show |
A | 3 | a0001c0002t0002g0193a0001c0002t0002g0194a0001c0002t0002g0195 | 3 | NA18955.hp2 NA19005.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1074+3934_1074+395 others(25): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238254 | |||||
chr22:29238362
|
C | A | 4 | a0001c0002t0001g0211a0001c0002t0001g0212a0001c0002t0001g0301others(1): Show | 4 | HG03139.hp2 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+4013C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238362 | ||||||
chr22:29238424
|
T | C | 56 | a0001c0002t0002g0192a0003c0003t0001g0028a0003c0003t0001g0210others(53): Show | 57 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1074+4075T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238424 | ||||||
chr22:29238489
|
C | G | 1 | a0001c0002t0001g0247 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1074+4140C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238489 | ||||||
chr22:29238513
|
G | A | 49 | a0001c0002t0001g0093a0001c0002t0001g0124a0001c0002t0001g0236others(46): Show | 49 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.1074+4164G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238513 | ||||||
chr22:29238715
|
G | A | 130 | a0001c0002t0001g0063a0001c0002t0001g0093a0001c0002t0001g0097others(127): Show | 131 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.1074+4366G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238715 | ||||||
chr22:29238719
|
AT | A | 64 | a0001c0002t0001g0030a0001c0002t0001g0305a0001c0002t0002g0077others(61): Show | 65 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1074+4390delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238719 | |||||
chr22:29238719
|
ATT | A | 125 | a0001c0002t0001g0063a0001c0002t0001g0093a0001c0002t0001g0097others(122): Show | 126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1074+4389_1074+439 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29238719 | |||||
chr22:29238739
|
T | A | 1 | a0002c0001t0001g0270 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1074+4390T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238739 | ||||||
chr22:29238778
|
G | T | 59 | a0001c0002t0002g0192a0003c0003t0001g0028a0003c0003t0001g0210others(56): Show | 60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1074+4429G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29238778 | ||||||
chr22:29239299
|
AT | A | 129 | a0001c0002t0001g0063a0001c0002t0001g0093a0001c0002t0001g0097others(126): Show | 130 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1075-4137delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29239299 | |||||
chr22:29239300
|
T | A | 1 | a0002c0001t0002g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1075-4145T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239300 | ||||||
chr22:29239322
|
G | A | 130 | a0001c0002t0001g0063a0001c0002t0001g0093a0001c0002t0001g0097others(127): Show | 131 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.1075-4123G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239322 | ||||||
chr22:29239323
|
G | T | 2 | a0001c0002t0001g0030a0001c0009t0001g0281 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1075-4122G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239323 | ||||||
chr22:29239413
|
G | A | 1 | a0002c0001t0001g0141 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1075-4032G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239413 | ||||||
chr22:29239430
|
C | T | 198 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1075-4015C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239430 | ||||||
chr22:29239456
|
C | T | 1 | a0004c0004t0003g0221 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1075-3989C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239456 | ||||||
chr22:29239468
|
C | A | 1 | a0004c0004t0003g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1075-3977C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239468 | ||||||
chr22:29239692
|
C | G | 1 | a0001c0002t0002g0242 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1075-3753C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239692 | ||||||
chr22:29239745
|
A | G | 1 | a0003c0003t0003g0205 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1075-3700A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239745 | ||||||
chr22:29239761
|
C | CT | 39 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0239others(36): Show | 39 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1075-3670dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29239761 | |||||
chr22:29239786
|
C | G | 1 | a0005c0006t0003g0066 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1075-3659C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239786 | ||||||
chr22:29239869
|
C | T | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1075-3576C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239869 | ||||||
chr22:29239873
|
CATCAACC others(45): Show |
C | 59 | a0001c0002t0002g0192a0003c0003t0001g0028a0003c0003t0001g0210others(56): Show | 60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1075-3537_1075-348 others(56): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29239873 | |||||
chr22:29239879
|
C | T | 6 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(3): Show | 7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-3566C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239879 | ||||||
chr22:29239904
|
C | T | 1 | a0001c0002t0001g0236 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1075-3541C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29239904 | ||||||
chr22:29240013
|
G | A | 198 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1075-3432G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240013 | ||||||
chr22:29240121
|
A | G | 3 | a0001c0002t0002g0223a0002c0001t0001g0068a0002c0001t0001g0089 | 3 | HG01192.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1075-3324A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240121 | ||||||
chr22:29240152
|
T | A | 198 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1075-3293T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240152 | ||||||
chr22:29240274
|
T | C | 1 | a0002c0001t0002g0246 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1075-3171T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240274 | ||||||
chr22:29240394
|
AAG | A | 127 | a0001c0002t0001g0063a0001c0002t0001g0093a0001c0002t0001g0097others(124): Show | 128 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.1075-3048_1075-304 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29240394 | |||||
chr22:29240397
|
A | G | 1 | a0001c0002t0003g0055 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1075-3048A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240397 | ||||||
chr22:29240567
|
G | C | 4 | a0001c0002t0001g0211a0001c0002t0001g0212a0001c0002t0001g0301others(1): Show | 4 | HG03139.hp2 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1075-2878G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240567 | ||||||
chr22:29240692
|
G | A | 6 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(3): Show | 7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-2753G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240692 | ||||||
chr22:29240724
|
T | A | 62 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0002t0003g0343others(59): Show | 63 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1075-2721T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240724 | ||||||
chr22:29240767
|
G | A | 2 | a0001c0002t0001g0030a0001c0009t0001g0281 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1075-2678G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240767 | ||||||
chr22:29240841
|
T | C | 62 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0002t0003g0343others(59): Show | 63 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1075-2604T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240841 | ||||||
chr22:29240852
|
A | T | 7 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(4): Show | 7 | HG02109.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-2593A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240852 | ||||||
chr22:29240879
|
G | A | 2 | a0001c0002t0002g0032a0001c0002t0002g0034 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1075-2566G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240879 | ||||||
chr22:29240884
|
C | A | 1 | a0002c0001t0001g0133 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1075-2561C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240884 | ||||||
chr22:29240996
|
C | T | 59 | a0001c0002t0002g0192a0003c0003t0001g0028a0003c0003t0001g0210others(56): Show | 60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1075-2449C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29240996 | ||||||
chr22:29241104
|
C | CTA | 62 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0002t0003g0343others(59): Show | 63 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1075-2340_1075-233 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29241104 | |||||
chr22:29241150
|
T | G | 8 | a0002c0001t0001g0110a0002c0001t0001g0153a0002c0001t0001g0154others(5): Show | 8 | NA18612.hp1 NA18942.hp2 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.1075-2295T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241150 | ||||||
chr22:29241255
|
T | C | 46 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(43): Show | 47 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(44): Show |
intron_variant | MODIFIER | c.1075-2190T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241255 | ||||||
chr22:29241292
|
G | T | 6 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(3): Show | 7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-2153G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241292 | ||||||
chr22:29241361
|
CTTG | C | 6 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(3): Show | 7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-2078_1075-207 others(7): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29241361 | |||||
chr22:29241568
|
T | G | 7 | a0003c0003t0003g0088a0004c0004t0002g0145a0004c0004t0003g0103others(4): Show | 7 | NA18940.hp1 NA18944.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-1877T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241568 | ||||||
chr22:29241578
|
G | GA | 59 | a0001c0002t0002g0192a0003c0003t0001g0028a0003c0003t0001g0210others(56): Show | 60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1075-1867_1075-186 others(5): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241578 | ||||||
chr22:29241622
|
C | T | 1 | a0001c0002t0002g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1075-1823C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241622 | ||||||
chr22:29241631
|
C | T | 3 | a0001c0002t0002g0200a0001c0002t0002g0303a0001c0002t0002g0304 | 3 | HG01243.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1075-1814C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241631 | ||||||
chr22:29241635
|
C | T | 51 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0229others(48): Show | 52 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.1075-1810C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241635 | ||||||
chr22:29241636
|
G | A | 82 | a0001c0002t0001g0019a0001c0002t0001g0036a0001c0002t0001g0037others(79): Show | 83 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.1075-1809G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241636 | ||||||
chr22:29241669
|
G | C | 34 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0239others(31): Show | 34 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.1075-1776G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241669 | ||||||
chr22:29241793
|
A | AT | 51 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0229others(48): Show | 52 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.1075-1645dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29241793 | |||||
chr22:29241899
|
G | A | 2 | a0001c0002t0001g0269a0001c0002t0002g0271 | 2 | HG02602.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1075-1546G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241899 | ||||||
chr22:29241950
|
A | G | 163 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(160): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1075-1495A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29241950 | ||||||
chr22:29242028
|
A | G | 1 | a0005c0006t0003g0066 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1075-1417A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29242028 | ||||||
chr22:29242220
|
C | T | 2 | a0001c0002t0002g0094a0001c0002t0002g0227 | 2 | HG00741.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1075-1225C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29242220 | ||||||
chr22:29242398
|
A | T | 62 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0002t0003g0343others(59): Show | 63 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1075-1047A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29242398 | ||||||
chr22:29242481
|
G | A | 30 | a0001c0002t0001g0018a0001c0002t0001g0117a0002c0001t0001g0023others(27): Show | 30 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.1075-964G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29242481 | ||||||
chr22:29242507
|
A | G | 1 | a0001c0002t0003g0343 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1075-938A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29242507 | ||||||
chr22:29243015
|
C | A | 1 | a0001c0002t0002g0191 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1075-430C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243015 | ||||||
chr22:29243047
|
C | T | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1075-398C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243047 | ||||||
chr22:29243072
|
C | T | 1 | a0001c0002t0003g0142 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1075-373C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243072 | ||||||
chr22:29243101
|
C | T | 59 | a0001c0002t0002g0192a0003c0003t0001g0028a0003c0003t0001g0210others(56): Show | 60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1075-344C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243101 | ||||||
chr22:29243126
|
T | C | 1 | a0001c0002t0002g0201 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1075-319T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243126 | ||||||
chr22:29243146
|
CT | C | 163 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(160): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1075-297delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr22 | 29243146 | |||||
chr22:29243172
|
A | G | 60 | a0001c0002t0001g0030a0001c0002t0002g0192a0003c0003t0001g0028others(57): Show | 61 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.1075-273A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243172 | ||||||
chr22:29243203
|
C | T | 163 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(160): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1075-242C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243203 | ||||||
chr22:29243389
|
G | A | 6 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(3): Show | 7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1075-56G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 12/14 | chr22 | 29243389 | ||||||
chr22:29243725
|
C | T | 1 | a0002c0001t0001g0257 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1119+236C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29243725 | ||||||
chr22:29243838
|
A | G | 1 | a0002c0001t0002g0286 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1119+349A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29243838 | ||||||
chr22:29243960
|
G | A | 1 | a0001c0002t0001g0248 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1119+471G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29243960 | ||||||
chr22:29244013
|
A | G | 4 | a0003c0003t0005g0282a0003c0003t0005g0283a0003c0003t0005g0322others(1): Show | 4 | HG02145.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+524A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244013 | ||||||
chr22:29244030
|
C | T | 59 | a0001c0002t0002g0192a0003c0003t0001g0028a0003c0003t0001g0210others(56): Show | 60 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1119+541C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244030 | ||||||
chr22:29244245
|
A | G | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1119+756A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244245 | ||||||
chr22:29244262
|
C | T | 4 | a0003c0003t0001g0028a0003c0003t0001g0318a0003c0003t0001g0319others(1): Show | 4 | HG01496.hp1 HG02055.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+773C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244262 | ||||||
chr22:29244320
|
G | A | 60 | a0001c0002t0001g0030a0001c0002t0002g0192a0003c0003t0001g0028others(57): Show | 61 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.1119+831G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244320 | ||||||
chr22:29244378
|
G | T | 6 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(3): Show | 7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119+889G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244378 | ||||||
chr22:29244383
|
G | A | 1 | a0002c0001t0001g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1119+894G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244383 | ||||||
chr22:29244524
|
A | C | 51 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0229others(48): Show | 52 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.1119+1035A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244524 | ||||||
chr22:29244650
|
AAG | A | 47 | a0003c0003t0001g0028a0003c0003t0001g0210a0003c0003t0001g0226others(44): Show | 48 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.1119+1163_1119+116 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29244650 | |||||
chr22:29244651
|
AG | A | 11 | a0001c0002t0002g0192a0003c0003t0001g0333a0003c0003t0003g0016others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1119+1163delG | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244651 | ||||||
chr22:29244657
|
G | A | 61 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0009t0001g0281others(58): Show | 62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1168G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244657 | ||||||
chr22:29244662
|
G | A | 61 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0009t0001g0281others(58): Show | 62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1173G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244662 | ||||||
chr22:29244667
|
T | C | 31 | a0001c0002t0001g0019a0001c0002t0001g0036a0001c0002t0001g0037others(28): Show | 31 | HG01081.hp2 HG01099.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1119+1178T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244667 | ||||||
chr22:29244667
|
T | G | 61 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0009t0001g0281others(58): Show | 62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1178T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244667 | ||||||
chr22:29244716
|
G | A | 39 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0229others(36): Show | 40 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.1119+1227G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244716 | ||||||
chr22:29244731
|
T | A | 61 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0009t0001g0281others(58): Show | 62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1242T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244731 | ||||||
chr22:29244748
|
C | T | 6 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(3): Show | 7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119+1259C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244748 | ||||||
chr22:29244757
|
A | AAGACG | 39 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0229others(36): Show | 40 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.1119+1271_1119+127 others(9): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29244757 | |||||
chr22:29244840
|
G | A | 1 | a0001c0002t0001g0018 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1119+1351G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244840 | ||||||
chr22:29244856
|
G | A | 1 | a0002c0001t0001g0079 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1119+1367G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244856 | ||||||
chr22:29244912
|
G | T | 1 | a0002c0001t0001g0341 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1119+1423G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29244912 | ||||||
chr22:29245029
|
T | C | 61 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0009t0001g0281others(58): Show | 62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1540T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245029 | ||||||
chr22:29245069
|
C | CT | 61 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0009t0001g0281others(58): Show | 62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1581dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29245069 | |||||
chr22:29245106
|
C | G | 61 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0009t0001g0281others(58): Show | 62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1617C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245106 | ||||||
chr22:29245188
|
C | T | 1 | a0001c0002t0001g0305 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1119+1699C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245188 | ||||||
chr22:29245189
|
G | A | 2 | a0003c0003t0003g0015a0003c0003t0003g0016 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1119+1700G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245189 | ||||||
chr22:29245289
|
A | G | 61 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0009t0001g0281others(58): Show | 62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1800A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245289 | ||||||
chr22:29245338
|
T | C | 61 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0009t0001g0281others(58): Show | 62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+1849T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245338 | ||||||
chr22:29245405
|
C | A | 6 | a0001c0002t0001g0173a0001c0002t0001g0175a0001c0002t0002g0123others(3): Show | 6 | NA18939.hp2 NA18943.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+1916C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245405 | ||||||
chr22:29245451
|
G | A | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1119+1962G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245451 | ||||||
chr22:29245479
|
C | A | 5 | a0001c0002t0001g0229a0002c0001t0001g0005a0002c0001t0001g0276others(2): Show | 6 | HG00099.hp1 HG01074.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+1990C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245479 | ||||||
chr22:29245562
|
T | C | 61 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0009t0001g0281others(58): Show | 62 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1119+2073T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245562 | ||||||
chr22:29245566
|
G | A | 1 | a0002c0001t0001g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1119+2077G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245566 | ||||||
chr22:29245579
|
G | A | 1 | a0002c0001t0001g0149 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1119+2090G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245579 | ||||||
chr22:29245672
|
T | C | 1 | a0002c0001t0001g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1119+2183T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245672 | ||||||
chr22:29245706
|
C | T | 58 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0009t0001g0281others(55): Show | 59 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1119+2217C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245706 | ||||||
chr22:29245750
|
G | A | 42 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0229others(39): Show | 43 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(40): Show |
intron_variant | MODIFIER | c.1119+2261G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245750 | ||||||
chr22:29245752
|
G | T | 56 | a0001c0002t0002g0192a0003c0003t0001g0028a0003c0003t0001g0210others(53): Show | 57 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1119+2263G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245752 | ||||||
chr22:29245758
|
G | C | 7 | a0001c0002t0001g0014a0001c0002t0001g0315a0001c0002t0002g0013others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1119+2269G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245758 | ||||||
chr22:29245868
|
C | T | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1119+2379C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245868 | ||||||
chr22:29245941
|
C | T | 2 | a0001c0002t0001g0059a0001c0002t0001g0060 | 2 | NA18952.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1119+2452C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29245941 | ||||||
chr22:29246008
|
A | G | 164 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1119+2519A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246008 | ||||||
chr22:29246023
|
A | G | 5 | a0004c0004t0001g0057a0004c0004t0003g0071a0004c0004t0003g0081others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119+2534A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246023 | ||||||
chr22:29246109
|
G | A | 1 | a0001c0002t0001g0315 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1119+2620G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246109 | ||||||
chr22:29246111
|
A | C | 2 | a0004c0004t0003g0215a0004c0004t0003g0216 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1119+2622A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246111 | ||||||
chr22:29246122
|
A | G | 58 | a0001c0002t0001g0030a0001c0002t0002g0192a0001c0009t0001g0281others(55): Show | 59 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1119+2633A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246122 | ||||||
chr22:29246148
|
T | C | 1 | a0001c0002t0003g0214 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1119+2659T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246148 | ||||||
chr22:29246275
|
G | A | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1119+2786G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246275 | ||||||
chr22:29246310
|
A | C | 4 | a0001c0002t0002g0125a0001c0002t0002g0126a0001c0002t0002g0127others(1): Show | 4 | NA18948.hp1 NA19000.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+2821A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246310 | ||||||
chr22:29246376
|
G | A | 129 | a0001c0002t0001g0063a0001c0002t0001g0093a0001c0002t0001g0097others(126): Show | 130 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1119+2887G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246376 | ||||||
chr22:29246384
|
C | T | 1 | a0002c0001t0001g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1119+2895C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246384 | ||||||
chr22:29246394
|
T | C | 3 | a0004c0004t0003g0118a0004c0004t0003g0185a0004c0004t0003g0209 | 3 | NA18973.hp2 NA18986.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1119+2905T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246394 | ||||||
chr22:29246397
|
C | T | 7 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(4): Show | 7 | HG02109.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1119+2908C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246397 | ||||||
chr22:29246463
|
G | C | 6 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(3): Show | 7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119+2974G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246463 | ||||||
chr22:29246468
|
G | A | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1119+2979G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246468 | ||||||
chr22:29246503
|
G | A | 44 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(41): Show | 45 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.1119+3014G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246503 | ||||||
chr22:29246534
|
G | C | 2 | a0001c0002t0001g0030a0001c0009t0001g0281 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1119+3045G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246534 | ||||||
chr22:29246599
|
G | A | 46 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(43): Show | 47 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(44): Show |
intron_variant | MODIFIER | c.1119+3110G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246599 | ||||||
chr22:29246841
|
C | A | 18 | a0001c0002t0001g0285a0001c0002t0002g0031a0001c0002t0002g0191others(15): Show | 19 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.1119+3352C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246841 | ||||||
chr22:29246853
|
A | G | 1 | a0003c0003t0003g0298 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1119+3364A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246853 | ||||||
chr22:29246859
|
C | T | 1 | a0002c0001t0001g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1119+3370C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29246859 | ||||||
chr22:29247096
|
A | T | 2 | a0004c0004t0003g0215a0004c0004t0003g0216 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1119+3607A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247096 | ||||||
chr22:29247218
|
G | A | 1 | a0001c0002t0003g0343 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1119+3729G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247218 | ||||||
chr22:29247305
|
A | G | 46 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(43): Show | 47 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(44): Show |
intron_variant | MODIFIER | c.1119+3816A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247305 | ||||||
chr22:29247360
|
T | A | 1 | a0002c0001t0001g0087 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1119+3871T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247360 | ||||||
chr22:29247382
|
C | T | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1119+3893C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247382 | ||||||
chr22:29247432
|
G | A | 164 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1119+3943G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247432 | ||||||
chr22:29247532
|
C | T | 7 | a0001c0002t0001g0063a0001c0002t0001g0097a0001c0002t0001g0178others(4): Show | 7 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(4): Show |
intron_variant | MODIFIER | c.1119+4043C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247532 | ||||||
chr22:29247549
|
A | C | 13 | a0002c0001t0001g0023a0002c0001t0001g0056a0002c0001t0001g0064others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1119+4060A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247549 | ||||||
chr22:29247670
|
G | A | 44 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(41): Show | 45 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.1119+4181G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247670 | ||||||
chr22:29247787
|
G | A | 6 | a0001c0002t0001g0211a0001c0002t0001g0212a0001c0002t0001g0300others(3): Show | 6 | HG03130.hp1 HG03139.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+4298G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247787 | ||||||
chr22:29247812
|
G | A | 4 | a0003c0003t0005g0282a0003c0003t0005g0283a0003c0003t0005g0322others(1): Show | 4 | HG02145.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+4323G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247812 | ||||||
chr22:29247948
|
CT | C | 57 | a0001c0002t0002g0192a0002c0001t0001g0078a0003c0003t0001g0028others(54): Show | 58 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1119+4473delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29247948 | |||||
chr22:29247970
|
A | G | 2 | a0001c0002t0001g0052a0001c0008t0002g0047 | 2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1119+4481A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29247970 | ||||||
chr22:29248038
|
G | A | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1119+4549G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248038 | ||||||
chr22:29248188
|
A | G | 1 | a0001c0002t0001g0305 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1119+4699A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248188 | ||||||
chr22:29248220
|
A | G | 6 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(3): Show | 7 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119+4731A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248220 | ||||||
chr22:29248259
|
C | CT | 23 | a0001c0002t0001g0063a0001c0002t0001g0250a0001c0002t0001g0300others(20): Show | 23 | HG00423.hp2 HG00597.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1119+4791dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29248259 | |||||
chr22:29248259
|
CT | C | 11 | a0001c0002t0001g0117a0001c0002t0001g0188a0001c0002t0001g0189others(8): Show | 11 | HG01175.hp1 HG02109.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1119+4791delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29248259 | |||||
chr22:29248259
|
CTT | C | 40 | a0001c0002t0001g0018a0001c0002t0001g0239a0001c0002t0002g0223others(37): Show | 40 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.1119+4790_1119+479 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29248259 | |||||
chr22:29248259
|
CTTT | C | 56 | a0001c0002t0001g0229a0001c0002t0002g0192a0001c0002t0002g0200others(53): Show | 58 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1119+4789_1119+479 others(7): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29248259 | |||||
chr22:29248259
|
CTTTT | C | 19 | a0001c0002t0001g0030a0001c0002t0001g0091a0001c0002t0001g0108others(16): Show | 19 | HG01192.hp1 HG01243.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.1119+4788_1119+479 others(8): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29248259 | |||||
chr22:29248259
|
CTTTTT | C | 45 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0060others(42): Show | 47 | HG00558.hp1 HG00609.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.1119+4787_1119+479 others(9): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29248259 | |||||
chr22:29248281
|
C | A | 1 | a0001c0002t0001g0116 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1119+4792C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248281 | ||||||
chr22:29248790
|
G | A | 1 | a0006c0007t0003g0187 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1119+5301G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248790 | ||||||
chr22:29248818
|
GC | G | 163 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(160): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1119+5330delC | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248818 | ||||||
chr22:29248942
|
G | A | 9 | a0001c0002t0002g0043a0001c0002t0002g0044a0001c0002t0002g0072others(6): Show | 9 | HG00544.hp2 NA18944.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.1120-5261G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248942 | ||||||
chr22:29248972
|
A | G | 13 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0091others(10): Show | 13 | HG00558.hp1 HG00609.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.1120-5231A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29248972 | ||||||
chr22:29249237
|
T | C | 5 | a0001c0002t0001g0229a0002c0001t0001g0005a0002c0001t0001g0276others(2): Show | 6 | HG00099.hp1 HG01074.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-4966T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249237 | ||||||
chr22:29249246
|
C | CT | 5 | a0002c0001t0001g0293a0002c0001t0002g0295a0002c0001t0002g0309others(2): Show | 5 | HG01070.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120-4949dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249246 | |||||
chr22:29249258
|
A | G | 5 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(2): Show | 6 | HG01884.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-4945A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249258 | ||||||
chr22:29249275
|
G | C | 164 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1120-4928G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249275 | ||||||
chr22:29249338
|
C | T | 1 | a0001c0002t0002g0266 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1120-4865C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249338 | ||||||
chr22:29249386
|
G | A | 164 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1120-4817G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249386 | ||||||
chr22:29249397
|
G | A | 164 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1120-4806G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249397 | ||||||
chr22:29249411
|
C | T | 164 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1120-4792C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249411 | ||||||
chr22:29249418
|
G | A | 2 | a0001c0002t0004g0026a0003c0003t0002g0325 | 2 | HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1120-4785G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249418 | ||||||
chr22:29249567
|
C | T | 5 | a0004c0004t0001g0057a0004c0004t0003g0071a0004c0004t0003g0081others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120-4636C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249567 | ||||||
chr22:29249587
|
A | ATTAT | 30 | a0001c0002t0001g0091a0001c0002t0001g0108a0001c0002t0001g0137others(27): Show | 30 | HG00544.hp2 HG00609.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1120-4577_1120-457 others(8): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | |||||
chr22:29249587
|
A | ATTATTTA others(1): Show |
6 | a0001c0002t0002g0191a0001c0002t0002g0317a0001c0002t0003g0196others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-4581_1120-457 others(12): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | |||||
chr22:29249587
|
A | ATTATTTA others(5): Show |
2 | a0001c0002t0001g0305a0006c0007t0003g0187 | 2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1120-4585_1120-457 others(16): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | |||||
chr22:29249587
|
A | ATTTATTA others(1): Show |
17 | a0001c0002t0001g0019a0001c0002t0001g0036a0001c0002t0001g0037others(14): Show | 17 | HG01081.hp2 HG01255.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1120-4614_1120-461 others(12): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | |||||
chr22:29249587
|
A | ATTTATTA others(5): Show |
11 | a0001c0002t0001g0052a0001c0002t0001g0189a0001c0002t0001g0190others(8): Show | 11 | HG01243.hp1 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1120-4614_1120-461 others(16): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | |||||
chr22:29249587
|
A | ATTTATTA others(9): Show |
1 | a0001c0002t0003g0343 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1120-4614_1120-461 others(20): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | |||||
chr22:29249587
|
ATTAT | A | 42 | a0001c0002t0001g0014a0001c0002t0001g0211a0001c0002t0001g0212others(39): Show | 42 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.1120-4577_1120-457 others(8): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | |||||
chr22:29249587
|
ATTATTTA others(1): Show |
A | 43 | a0001c0002t0001g0018a0001c0002t0001g0117a0001c0002t0001g0229others(40): Show | 44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1120-4581_1120-457 others(12): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249587 | |||||
chr22:29249590
|
ATTTAT | A | 6 | a0001c0002t0001g0173a0001c0002t0001g0175a0001c0002t0002g0123others(3): Show | 6 | NA18939.hp2 NA18943.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-4610_1120-460 others(9): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29249590 | |||||
chr22:29249640
|
G | T | 1 | a0001c0002t0001g0256 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1120-4563G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249640 | ||||||
chr22:29249667
|
G | T | 164 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1120-4536G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249667 | ||||||
chr22:29249671
|
A | G | 1 | a0001c0002t0002g0242 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1120-4532A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249671 | ||||||
chr22:29249768
|
C | G | 164 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1120-4435C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249768 | ||||||
chr22:29249787
|
G | A | 164 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1120-4416G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249787 | ||||||
chr22:29249906
|
C | T | 56 | a0001c0002t0002g0192a0003c0003t0001g0028a0003c0003t0001g0210others(53): Show | 57 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.1120-4297C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249906 | ||||||
chr22:29249914
|
C | T | 5 | a0002c0001t0001g0133a0002c0001t0003g0002a0002c0001t0003g0129others(2): Show | 6 | NA18955.hp1 NA18963.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-4289C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29249914 | ||||||
chr22:29250106
|
A | G | 108 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(105): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1120-4097A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250106 | ||||||
chr22:29250225
|
C | T | 1 | a0002c0001t0007g0161 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1120-3978C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250225 | ||||||
chr22:29250285
|
AATCAAGG others(12): Show |
A | 1 | a0001c0002t0006g0020 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1120-3917_1120-389 others(23): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250285 | ||||||
chr22:29250286
|
A | G | 163 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(160): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1120-3917A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250286 | ||||||
chr22:29250311
|
G | T | 1 | a0001c0002t0002g0203 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1120-3892G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250311 | ||||||
chr22:29250313
|
T | G | 1 | a0001c0002t0002g0203 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1120-3890T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250313 | ||||||
chr22:29250450
|
A | C | 164 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1120-3753A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250450 | ||||||
chr22:29250489
|
C | T | 1 | a0002c0001t0001g0029 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1120-3714C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250489 | ||||||
chr22:29250539
|
G | A | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1120-3664G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250539 | ||||||
chr22:29250544
|
A | T | 2 | a0001c0002t0003g0184a0002c0001t0003g0128 | 2 | NA18971.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1120-3659A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250544 | ||||||
chr22:29250561
|
C | CT | 172 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(169): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1120-3632dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250561 | |||||
chr22:29250624
|
T | C | 1 | a0003c0003t0003g0139 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1120-3579T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250624 | ||||||
chr22:29250630
|
G | A | 1 | a0001c0002t0003g0179 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1120-3573G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250630 | ||||||
chr22:29250733
|
A | AT | 11 | a0001c0002t0001g0285a0001c0002t0001g0331a0001c0002t0002g0191others(8): Show | 11 | HG00741.hp1 HG01192.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1120-3435dupT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
A | ATTTT | 5 | a0001c0002t0002g0031a0001c0002t0002g0291a0001c0002t0004g0001others(2): Show | 6 | HG01884.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-3438_1120-343 others(8): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
A | ATTTTTTT | 18 | a0001c0002t0001g0229a0001c0002t0001g0239a0001c0002t0002g0223others(15): Show | 18 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(15): Show |
intron_variant | MODIFIER | c.1120-3441_1120-343 others(11): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
A | ATTTTTTT others(1): Show |
16 | a0001c0002t0001g0018a0001c0002t0001g0117a0002c0001t0001g0005others(13): Show | 17 | HG01081.hp1 HG01109.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1120-3442_1120-343 others(12): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
A | ATTTTTTT others(2): Show |
6 | a0002c0001t0001g0023a0002c0001t0001g0089a0002c0001t0001g0141others(3): Show | 6 | HG00733.hp2 HG01167.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1120-3443_1120-343 others(13): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
A | ATTTTTTT others(3): Show |
1 | a0002c0001t0003g0099 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1120-3444_1120-343 others(14): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
A | ATTTTTTT others(4): Show |
1 | a0002c0001t0001g0049 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1120-3445_1120-343 others(15): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
A | ATTTTTTT others(5): Show |
2 | a0002c0001t0001g0048a0002c0001t0002g0106 | 2 | HG01257.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1120-3446_1120-343 others(16): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
A | ATTTTTTT others(6): Show |
1 | a0002c0001t0001g0039 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1120-3447_1120-343 others(17): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
AT | A | 35 | a0001c0002t0001g0297a0001c0002t0001g0300a0001c0002t0001g0301others(32): Show | 36 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1120-3435delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
ATT | A | 38 | a0001c0002t0001g0019a0001c0002t0001g0030a0001c0002t0001g0189others(35): Show | 38 | HG00423.hp2 HG00544.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1120-3436_1120-343 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
ATTT | A | 122 | a0001c0002t0001g0036a0001c0002t0001g0037a0001c0002t0001g0052others(119): Show | 123 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1120-3437_1120-343 others(7): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
ATTTT | A | 13 | a0001c0002t0001g0190a0001c0002t0001g0251a0001c0002t0001g0255others(10): Show | 13 | HG00099.hp2 HG01070.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1120-3438_1120-343 others(8): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
ATTTTTTT others(6): Show |
A | 1 | a0002c0001t0001g0134 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1120-3447_1120-343 others(17): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
ATTTTTTT others(7): Show |
A | 42 | a0001c0002t0001g0014a0001c0002t0001g0059a0001c0002t0001g0091others(39): Show | 43 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1120-3448_1120-343 others(18): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
ATTTTTTT others(8): Show |
A | 2 | a0001c0002t0001g0060a0002c0001t0003g0130 | 2 | NA18986.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1120-3449_1120-343 others(19): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250733
|
ATTTTTTT others(9): Show |
A | 3 | a0002c0001t0001g0294a0003c0003t0003g0058a0003c0003t0003g0260 | 3 | HG02015.hp1 HG03209.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1120-3450_1120-343 others(20): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29250733 | |||||
chr22:29250818
|
C | T | 1 | a0001c0002t0001g0239 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1120-3385C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29250818 | ||||||
chr22:29251053
|
A | T | 22 | a0001c0002t0001g0019a0001c0002t0001g0036a0001c0002t0001g0037others(19): Show | 22 | HG01081.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1120-3150A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251053 | ||||||
chr22:29251093
|
T | A | 1 | a0002c0001t0001g0329 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1120-3110T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251093 | ||||||
chr22:29251117
|
C | T | 1 | a0003c0003t0003g0004 | 2 | NA18969.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1120-3086C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251117 | ||||||
chr22:29251124
|
G | A | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1120-3079G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251124 | ||||||
chr22:29251138
|
G | A | 164 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1120-3065G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251138 | ||||||
chr22:29251186
|
A | G | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1120-3017A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251186 | ||||||
chr22:29251226
|
C | T | 163 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(160): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.1120-2977C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251226 | ||||||
chr22:29251274
|
G | T | 164 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1120-2929G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251274 | ||||||
chr22:29251333
|
C | T | 4 | a0001c0002t0003g0218a0001c0002t0003g0233a0002c0001t0003g0217others(1): Show | 4 | HG00280.hp2 HG02132.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120-2870C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251333 | ||||||
chr22:29251382
|
AT | A | 296 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0030others(293): Show | 299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.1120-2805delT | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29251382 | |||||
chr22:29251382
|
ATT | A | 8 | a0001c0002t0001g0229a0002c0001t0001g0005a0002c0001t0001g0244others(5): Show | 9 | HG00099.hp1 HG01074.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.1120-2806_1120-280 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29251382 | |||||
chr22:29251490
|
C | T | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1120-2713C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251490 | ||||||
chr22:29251509
|
G | A | 2 | a0001c0002t0002g0032a0001c0002t0002g0034 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1120-2694G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251509 | ||||||
chr22:29251795
|
A | G | 167 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(164): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1120-2408A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251795 | ||||||
chr22:29251865
|
A | G | 55 | a0001c0002t0002g0192a0002c0001t0001g0240a0003c0003t0001g0028others(52): Show | 56 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1120-2338A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251865 | ||||||
chr22:29251967
|
C | T | 3 | a0003c0003t0001g0333a0003c0003t0001g0334a0003c0003t0001g0335 | 3 | HG02258.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1120-2236C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29251967 | ||||||
chr22:29252108
|
G | A | 1 | a0001c0002t0002g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1120-2095G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252108 | ||||||
chr22:29252146
|
C | T | 1 | a0001c0009t0001g0281 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1120-2057C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252146 | ||||||
chr22:29252176
|
T | C | 166 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(163): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1120-2027T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252176 | ||||||
chr22:29252190
|
C | T | 4 | a0003c0003t0005g0282a0003c0003t0005g0283a0003c0003t0005g0322others(1): Show | 4 | HG02145.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120-2013C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252190 | ||||||
chr22:29252226
|
T | A | 42 | a0001c0002t0001g0014a0001c0002t0001g0091a0001c0002t0001g0108others(39): Show | 43 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1120-1977T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252226 | ||||||
chr22:29252285
|
C | T | 42 | a0001c0002t0001g0014a0001c0002t0001g0091a0001c0002t0001g0108others(39): Show | 43 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1120-1918C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252285 | ||||||
chr22:29252362
|
G | T | 42 | a0001c0002t0001g0014a0001c0002t0001g0091a0001c0002t0001g0108others(39): Show | 43 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1120-1841G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252362 | ||||||
chr22:29252424
|
A | G | 2 | a0001c0002t0001g0030a0001c0009t0001g0281 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1120-1779A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252424 | ||||||
chr22:29252538
|
C | G | 2 | a0001c0002t0001g0030a0001c0009t0001g0281 | 2 | HG02970.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1120-1665C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252538 | ||||||
chr22:29252572
|
G | A | 2 | a0001c0002t0002g0032a0001c0002t0002g0034 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1120-1631G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252572 | ||||||
chr22:29252583
|
T | C | 12 | a0001c0002t0001g0285a0001c0002t0002g0191a0001c0002t0002g0197others(9): Show | 12 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1120-1620T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252583 | ||||||
chr22:29252615
|
A | T | 54 | a0001c0002t0002g0192a0003c0003t0001g0028a0003c0003t0001g0210others(51): Show | 55 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1120-1588A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252615 | ||||||
chr22:29252717
|
C | T | 1 | a0002c0001t0001g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1120-1486C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252717 | ||||||
chr22:29252772
|
C | G | 1 | a0003c0003t0003g0222 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1120-1431C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252772 | ||||||
chr22:29252939
|
G | A | 3 | a0001c0002t0001g0305a0001c0002t0003g0196a0006c0007t0003g0187 | 3 | HG02451.hp2 HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1120-1264G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252939 | ||||||
chr22:29252957
|
C | T | 5 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(2): Show | 6 | HG01884.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-1246C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29252957 | ||||||
chr22:29253215
|
C | T | 166 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0030others(163): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1120-988C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253215 | ||||||
chr22:29253309
|
G | A | 54 | a0001c0002t0002g0192a0003c0003t0001g0028a0003c0003t0001g0210others(51): Show | 55 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1120-894G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253309 | ||||||
chr22:29253321
|
G | A | 54 | a0001c0002t0002g0192a0003c0003t0001g0028a0003c0003t0001g0210others(51): Show | 55 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1120-882G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253321 | ||||||
chr22:29253353
|
C | T | 42 | a0001c0002t0001g0014a0001c0002t0001g0091a0001c0002t0001g0108others(39): Show | 43 | HG00558.hp1 HG00609.hp1 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.1120-850C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253353 | ||||||
chr22:29253355
|
G | T | 1 | a0001c0002t0001g0239 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1120-848G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253355 | ||||||
chr22:29253356
|
G | T | 1 | a0001c0002t0001g0239 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1120-847G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253356 | ||||||
chr22:29253382
|
A | G | 12 | a0001c0002t0001g0285a0001c0002t0002g0191a0001c0002t0002g0197others(9): Show | 12 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1120-821A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253382 | ||||||
chr22:29253389
|
C | T | 1 | a0001c0002t0003g0261 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1120-814C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253389 | ||||||
chr22:29253441
|
G | T | 1 | a0002c0001t0001g0164 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1120-762G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253441 | ||||||
chr22:29253466
|
C | A | 12 | a0001c0002t0001g0285a0001c0002t0002g0191a0001c0002t0002g0197others(9): Show | 12 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1120-737C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253466 | ||||||
chr22:29253487
|
CAGG | C | 54 | a0001c0002t0002g0192a0003c0003t0001g0028a0003c0003t0001g0210others(51): Show | 55 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1120-713_1120-711d others(5): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr22 | 29253487 | |||||
chr22:29253537
|
G | A | 1 | a0001c0002t0011g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1120-666G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253537 | ||||||
chr22:29253538
|
C | T | 1 | a0002c0001t0001g0039 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1120-665C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253538 | ||||||
chr22:29253592
|
T | C | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1120-611T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253592 | ||||||
chr22:29253593
|
G | A | 5 | a0001c0002t0002g0031a0001c0002t0002g0266a0001c0002t0002g0291others(2): Show | 6 | HG01884.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-610G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253593 | ||||||
chr22:29253725
|
C | G | 1 | a0002c0001t0001g0329 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1120-478C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253725 | ||||||
chr22:29253726
|
G | C | 1 | a0002c0001t0001g0329 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1120-477G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253726 | ||||||
chr22:29253743
|
G | C | 3 | a0003c0003t0003g0015a0003c0003t0003g0016a0004c0004t0003g0306 | 3 | HG02886.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1120-460G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253743 | ||||||
chr22:29253786
|
G | A | 15 | a0001c0002t0001g0019a0001c0002t0001g0297a0002c0001t0001g0006others(12): Show | 15 | HG01081.hp2 HG01243.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1120-417G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253786 | ||||||
chr22:29253855
|
T | G | 2 | a0001c0002t0004g0027a0001c0002t0011g0307 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1120-348T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253855 | ||||||
chr22:29253931
|
G | A | 2 | a0001c0002t0004g0027a0001c0002t0011g0307 | 2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1120-272G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253931 | ||||||
chr22:29253976
|
A | G | 1 | a0002c0001t0001g0080 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1120-227A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29253976 | ||||||
chr22:29254135
|
A | C | 1 | a0001c0002t0001g0239 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1120-68A>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29254135 | ||||||
chr22:29254137
|
C | T | 3 | a0003c0003t0002g0085a0003c0003t0003g0086a0003c0003t0003g0208 | 3 | NA18945.hp1 NA18953.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1120-66C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 13/14 | chr22 | 29254137 | ||||||
chr22:29254307
|
C | T | 1 | a0001c0002t0003g0179 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1204+20C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254307 | ||||||
chr22:29254469
|
C | T | 182 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(179): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1204+182C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254469 | ||||||
chr22:29254571
|
A | G | 1 | a0002c0001t0001g0293 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1204+284A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254571 | ||||||
chr22:29254588
|
T | A | 5 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0190others(2): Show | 5 | HG02630.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1204+301T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254588 | ||||||
chr22:29254660
|
C | A | 1 | a0006c0007t0003g0187 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1204+373C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254660 | ||||||
chr22:29254703
|
A | G | 199 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(196): Show | 203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1204+416A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254703 | ||||||
chr22:29254752
|
C | T | 43 | a0001c0002t0001g0018a0001c0002t0001g0030a0001c0002t0001g0059others(40): Show | 44 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.1204+465C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254752 | ||||||
chr22:29254785
|
C | T | 7 | a0001c0002t0001g0229a0002c0001t0001g0005a0002c0001t0001g0276others(4): Show | 8 | HG00099.hp1 HG01074.hp1 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.1204+498C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254785 | ||||||
chr22:29254916
|
C | T | 182 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(179): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1204+629C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254916 | ||||||
chr22:29254990
|
C | T | 1 | a0003c0003t0003g0004 | 2 | NA18969.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1204+703C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254990 | ||||||
chr22:29254998
|
G | A | 5 | a0001c0002t0001g0229a0002c0001t0001g0005a0002c0001t0001g0276others(2): Show | 6 | HG00099.hp1 HG01074.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1204+711G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29254998 | ||||||
chr22:29255004
|
C | T | 27 | a0001c0002t0001g0285a0001c0002t0002g0031a0001c0002t0002g0035others(24): Show | 28 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1204+717C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255004 | ||||||
chr22:29255031
|
CCTCA | C | 179 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(176): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1204+750_1204+753d others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 29255031 | |||||
chr22:29255116
|
T | A | 1 | a0004c0004t0003g0071 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1204+829T>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255116 | ||||||
chr22:29255202
|
C | T | 1 | a0001c0002t0001g0305 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1204+915C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255202 | ||||||
chr22:29255239
|
C | T | 1 | a0001c0002t0002g0105 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1204+952C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255239 | ||||||
chr22:29255336
|
C | T | 1 | a0002c0001t0002g0073 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1204+1049C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255336 | ||||||
chr22:29255641
|
G | A | 1 | a0001c0002t0002g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1204+1354G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255641 | ||||||
chr22:29255660
|
G | A | 1 | a0004c0004t0003g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1204+1373G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255660 | ||||||
chr22:29255788
|
C | A | 1 | a0002c0001t0001g0329 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1204+1501C>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255788 | ||||||
chr22:29255984
|
T | G | 1 | a0002c0001t0001g0329 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1204+1697T>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29255984 | ||||||
chr22:29256077
|
G | T | 1 | a0003c0003t0003g0139 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1204+1790G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256077 | ||||||
chr22:29256116
|
G | A | 4 | a0001c0002t0002g0200a0001c0002t0002g0290a0001c0002t0004g0026others(1): Show | 4 | HG02717.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204+1829G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256116 | ||||||
chr22:29256142
|
A | T | 1 | a0002c0001t0001g0329 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1204+1855A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256142 | ||||||
chr22:29256169
|
G | A | 58 | a0001c0002t0001g0063a0001c0002t0001g0097a0001c0002t0001g0108others(55): Show | 59 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1204+1882G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256169 | ||||||
chr22:29256201
|
G | A | 1 | a0001c0002t0002g0126 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1204+1914G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256201 | ||||||
chr22:29256226
|
A | T | 1 | a0002c0001t0001g0329 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1204+1939A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256226 | ||||||
chr22:29256239
|
G | A | 4 | a0001c0002t0001g0297a0002c0001t0003g0336a0002c0001t0003g0337others(1): Show | 4 | HG02257.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204+1952G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256239 | ||||||
chr22:29256289
|
A | G | 14 | a0001c0002t0001g0315a0001c0002t0002g0017a0001c0002t0002g0191others(11): Show | 14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1204+2002A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256289 | ||||||
chr22:29256347
|
C | G | 1 | a0001c0002t0002g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1204+2060C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256347 | ||||||
chr22:29256463
|
C | CA | 13 | a0001c0002t0001g0036a0001c0002t0001g0091a0001c0002t0002g0042others(10): Show | 13 | HG00741.hp2 HG01175.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.1204+2196dupA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 29256463 | |||||
chr22:29256463
|
CA | C | 15 | a0001c0002t0001g0143a0001c0002t0001g0315a0001c0002t0002g0038others(12): Show | 15 | HG01256.hp1 HG02080.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1204+2196delA | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 29256463 | |||||
chr22:29256463
|
CAA | C | 26 | a0001c0002t0002g0013a0001c0002t0002g0017a0001c0002t0002g0191others(23): Show | 27 | HG00741.hp1 HG01109.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1204+2195_1204+219 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 29256463 | |||||
chr22:29256466
|
A | T | 1 | a0002c0001t0001g0329 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1204+2179A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256466 | ||||||
chr22:29256664
|
C | T | 1 | a0002c0001t0002g0053 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1205-2153C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256664 | ||||||
chr22:29256678
|
A | G | 1 | a0001c0002t0003g0196 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1205-2139A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256678 | ||||||
chr22:29256782
|
A | G | 2 | a0001c0002t0003g0196a0006c0007t0003g0187 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1205-2035A>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256782 | ||||||
chr22:29256858
|
A | T | 1 | a0002c0001t0001g0329 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1205-1959A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256858 | ||||||
chr22:29256860
|
GGT | G | 5 | a0001c0002t0011g0307a0003c0003t0005g0282a0003c0003t0005g0283others(2): Show | 5 | HG02145.hp2 HG03098.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1205-1953_1205-195 others(6): Show |
EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr22 | 29256860 | |||||
chr22:29256975
|
C | T | 2 | a0001c0002t0003g0196a0006c0007t0003g0187 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1205-1842C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29256975 | ||||||
chr22:29257047
|
G | A | 1 | a0001c0002t0001g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1205-1770G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257047 | ||||||
chr22:29257066
|
A | T | 4 | a0001c0002t0002g0200a0001c0002t0004g0001a0001c0002t0004g0026others(1): Show | 5 | HG02647.hp1 HG02717.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1205-1751A>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257066 | ||||||
chr22:29257139
|
C | T | 7 | a0001c0002t0002g0013a0001c0002t0002g0277a0001c0002t0002g0288others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1205-1678C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257139 | ||||||
chr22:29257210
|
G | T | 1 | a0002c0001t0003g0111 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1205-1607G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257210 | ||||||
chr22:29257420
|
C | T | 20 | a0001c0002t0003g0003a0001c0002t0003g0061a0001c0002t0003g0142others(17): Show | 22 | HG00558.hp2 HG00609.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.1205-1397C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257420 | ||||||
chr22:29257421
|
G | A | 4 | a0002c0001t0003g0339a0004c0004t0003g0071a0004c0004t0003g0082others(1): Show | 4 | HG00099.hp1 HG00642.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1205-1396G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257421 | ||||||
chr22:29257495
|
G | C | 1 | a0002c0001t0001g0342 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1205-1322G>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257495 | ||||||
chr22:29257511
|
C | T | 2 | a0001c0002t0002g0192a0004c0004t0002g0323 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1205-1306C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257511 | ||||||
chr22:29257519
|
G | A | 2 | a0001c0002t0002g0032a0001c0002t0002g0034 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1205-1298G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257519 | ||||||
chr22:29257575
|
T | C | 334 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(331): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1205-1242T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257575 | ||||||
chr22:29257622
|
G | A | 117 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0036others(114): Show | 118 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.1205-1195G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257622 | ||||||
chr22:29257690
|
G | A | 2 | a0001c0002t0002g0252a0002c0001t0002g0246 | 2 | HG02080.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1205-1127G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257690 | ||||||
chr22:29257717
|
C | T | 7 | a0001c0002t0002g0013a0001c0002t0002g0277a0001c0002t0002g0288others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1205-1100C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257717 | ||||||
chr22:29257757
|
T | C | 20 | a0001c0002t0003g0003a0001c0002t0003g0061a0001c0002t0003g0142others(17): Show | 22 | HG00558.hp2 HG00609.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.1205-1060T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257757 | ||||||
chr22:29257766
|
C | T | 1 | a0002c0001t0003g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1205-1051C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257766 | ||||||
chr22:29257852
|
T | C | 1 | a0006c0007t0003g0187 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1205-965T>C | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257852 | ||||||
chr22:29257886
|
G | A | 13 | a0001c0002t0002g0012a0001c0002t0002g0017a0001c0002t0002g0191others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.1205-931G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257886 | ||||||
chr22:29257924
|
C | G | 4 | a0001c0002t0002g0252a0002c0001t0002g0246a0002c0001t0002g0299others(1): Show | 4 | HG02080.hp2 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1205-893C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257924 | ||||||
chr22:29257940
|
G | A | 1 | a0001c0002t0003g0316 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1205-877G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257940 | ||||||
chr22:29257940
|
G | T | 83 | a0001c0002t0002g0032a0001c0002t0002g0034a0001c0002t0002g0035others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1205-877G>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29257940 | ||||||
chr22:29258015
|
C | T | 175 | a0001c0002t0001g0014a0001c0002t0001g0018a0001c0002t0001g0019others(172): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1205-802C>T | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29258015 | ||||||
chr22:29258031
|
C | G | 1 | a0001c0002t0001g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1205-786C>G | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29258031 | ||||||
chr22:29258728
|
G | A | 1 | a0002c0001t0003g0311 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1205-89G>A | EMID1 | ENSG00000186998.16 | transcript | ENST00000334018.11 | protein_coding | 14/14 | chr22 | 29258728 |