geneid | 10847 |
---|---|
ensemblid | ENSG00000080603.17 |
hgncid | 16974 |
symbol | SRCAP |
name | Snf2 related CREBBP activator protein |
refseq_nuc | NM_006662.3 |
refseq_prot | NP_006653.2 |
ensembl_nuc | ENST00000262518.9 |
ensembl_prot | ENSP00000262518.4 |
mane_status | MANE Select |
chr | chr16 |
start | 30699171 |
end | 30741409 |
strand | + |
ver | v1.2 |
region | chr16:30699171-30741409 |
region5000 | chr16:30694171-30746409 |
regionname0 | SRCAP_chr16_30699171_30741409 |
regionname5000 | SRCAP_chr16_30694171_30746409 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 3230 | 185 | 60 | 49 | 47 | 12 | 15 | 32 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0002 | 0/0 | 3230 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0003 | 0/0 | 3230 | 3 | 1 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0004 | 0/0 | 3230 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0005 | 0/0 | 3230 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0006 | 0/0 | 3230 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0007 | 0/0 | 3230 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0008 | 0/0 | 3230 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0009 | 0/0 | 3230 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0010 | 0/0 | 3230 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0011 | 0/0 | 3230 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0012 | 0/0 | 3230 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0013 | 0/0 | 3230 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0014 | 0/0 | 3230 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
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 | 0/1 | 9693 | 157 | 38 | 46 | 46 | 12 | 14 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0002 | 1/0 | 9693 | 7 | 5 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0003 | 0/0 | 9693 | 7 | 6 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0004 | 0/0 | 9693 | 4 | 0 | 4 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0005 | 0/0 | 9693 | 4 | 4 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0006 | 0/0 | 9693 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0007 | 0/0 | 9693 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0008 | 0/0 | 9693 | 3 | 1 | 0 | 0 | 2 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0009 | 0/0 | 9693 | 2 | 0 | 0 | 1 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0010 | 0/0 | 9693 | 2 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0011 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0012 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0013 | 0/0 | 9693 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0014 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0015 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0016 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0017 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0018 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0019 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0020 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0021 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0022 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0023 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0024 | 0/0 | 9693 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0025 | 0/0 | 9693 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
c0026 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
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 | 0/0 | 2031 | 100 | 38 | 18 | 28 | 6 | 10 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
t0002 | 0/1 | 2032 | 81 | 10 | 33 | 25 | 6 | 6 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
t0003 | 1/0 | 2032 | 10 | 8 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
t0004 | 0/0 | 2030 | 5 | 3 | 1 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
t0005 | 0/0 | 2031 | 5 | 5 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
t0006 | 0/0 | 2032 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
t0007 | 0/0 | 2032 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
t0008 | 0/0 | 2032 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
t0009 | 0/0 | 2032 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
t0010 | 0/0 | 2032 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
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 | 13 | 1 | 7 | 4 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0002 | 0/0 | 11 | 0 | 3 | 5 | 0 | 3 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0004 | 0/1 | 4 | 0 | 2 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0034 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 9693 | 157 | 38 | 46 | 46 | 12 | 14 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0002 | 1/0 | 9693 | 7 | 5 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0003 | 0/0 | 9693 | 7 | 6 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0005 | 0/0 | 9693 | 4 | 4 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0007 | 0/0 | 9693 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0011 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0014 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0015 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0016 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0020 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0024 | 0/0 | 9693 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0025 | 0/0 | 9693 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0002c0004 | 0/0 | 9693 | 4 | 0 | 4 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0002c0013 | 0/0 | 9693 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0003c0008 | 0/0 | 9693 | 3 | 1 | 0 | 0 | 2 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0004c0006 | 0/0 | 9693 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0005c0010 | 0/0 | 9693 | 2 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0006c0009 | 0/0 | 9693 | 2 | 0 | 0 | 1 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0007c0026 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0008c0021 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0009c0019 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0010c0018 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0011c0017 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0012c0012 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0013c0022 | 0/0 | 9693 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0014c0023 | 0/0 | 9693 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 11723 | 80 | 30 | 14 | 22 | 6 | 8 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0001t0002 | 0/1 | 11724 | 65 | 0 | 31 | 23 | 4 | 6 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0001t0004 | 0/0 | 11722 | 4 | 3 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0001t0005 | 0/0 | 11723 | 5 | 5 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0001t0007 | 0/0 | 11724 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0001t0009 | 0/0 | 11724 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0001t0010 | 0/0 | 11724 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0002t0003 | 1/0 | 11724 | 7 | 5 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0003t0002 | 0/0 | 11724 | 7 | 6 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0005t0001 | 0/0 | 11723 | 4 | 4 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0007t0006 | 0/0 | 11724 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0011t0001 | 0/0 | 11723 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0014t0001 | 0/0 | 11723 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0015t0002 | 0/0 | 11724 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0016t0001 | 0/0 | 11723 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0020t0002 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0024t0001 | 0/0 | 11723 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0001c0025t0002 | 0/0 | 11724 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0002c0004t0001 | 0/0 | 11723 | 3 | 0 | 3 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0002c0004t0004 | 0/0 | 11722 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0002c0013t0001 | 0/0 | 11723 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0003c0008t0002 | 0/0 | 11724 | 3 | 1 | 0 | 0 | 2 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0004c0006t0003 | 0/0 | 11724 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0004c0006t0008 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0005c0010t0001 | 0/0 | 11723 | 2 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0006c0009t0001 | 0/0 | 11723 | 2 | 0 | 0 | 1 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0007c0026t0001 | 0/0 | 11723 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0008c0021t0002 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0009c0019t0001 | 0/0 | 11723 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0010c0018t0001 | 0/0 | 11723 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0011c0017t0001 | 0/0 | 11723 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0012c0012t0003 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0013c0022t0002 | 0/0 | 11724 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
a0014c0023t0002 | 0/0 | 11724 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | copy fasta | chr16 | 30694171 | 30746409 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0001 | 0/0 | 11 | 0 | 7 | 3 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0004 | 0/1 | 4 | 0 | 2 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0005g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0007g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0001t0010g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0002t0003g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0002t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0002t0003g0034 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0003t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0003t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0003t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0003t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0003t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0003t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0005t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0005t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0005t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0007t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0007t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0007t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0011t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0014t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0015t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0016t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0020t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0024t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0001c0025t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0002c0004t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0002c0004t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0002c0004t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0002c0013t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0003c0008t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0003c0008t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0003c0008t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0004c0006t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0004c0006t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0005c0010t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0005c0010t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0006c0009t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0007c0026t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0008c0021t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0009c0019t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0010c0018t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0011c0017t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0012c0012t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0013c0022t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
a0014c0023t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | GBR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0111 | EUR | GBR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | GBR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | FIN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | FIN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01069 | hp1 | a0002 | c0004 | t0001 | g0002 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01071 | hp2 | a0002 | c0004 | t0004 | g0002 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01109 | hp2 | a0001 | c0002 | t0003 | g0032 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01192 | hp1 | a0002 | c0004 | t0001 | g0002 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01243 | hp2 | a0001 | c0025 | t0002 | g0049 | AMR | PUR | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01496 | hp1 | a0001 | c0003 | t0002 | g0103 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01516 | hp1 | a0003 | c0008 | t0002 | g0098 | EUR | IBS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0084 | EUR | IBS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01517 | hp1 | a0003 | c0008 | t0002 | g0099 | EUR | IBS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0066 | EUR | IBS | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01884 | hp1 | a0012 | c0012 | t0003 | g0030 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01884 | hp2 | a0001 | c0003 | t0002 | g0154 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01891 | hp1 | a0001 | c0016 | t0001 | g0152 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01891 | hp2 | a0004 | c0006 | t0008 | g0031 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01943 | hp1 | a0002 | c0004 | t0001 | g0025 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01952 | hp2 | a0001 | c0001 | t0007 | g0102 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG01975 | hp2 | a0002 | c0013 | t0001 | g0155 | AMR | PEL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02040 | hp1 | a0001 | c0001 | t0009 | g0077 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02055 | hp1 | a0001 | c0005 | t0001 | g0137 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02132 | hp2 | a0006 | c0009 | t0001 | g0002 | EAS | KHV | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02145 | hp1 | a0001 | c0003 | t0002 | g0104 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02145 | hp2 | a0008 | c0021 | t0002 | g0093 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02257 | hp2 | a0013 | c0022 | t0002 | g0079 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02280 | hp2 | a0001 | c0007 | t0006 | g0028 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02738 | hp1 | a0001 | c0024 | t0001 | g0112 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0005 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02818 | hp1 | a0001 | c0005 | t0001 | g0133 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02886 | hp1 | a0001 | c0007 | t0006 | g0026 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02896 | hp1 | a0001 | c0003 | t0002 | g0105 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02965 | hp2 | a0001 | c0002 | t0003 | g0029 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02970 | hp2 | a0001 | c0005 | t0001 | g0134 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03139 | hp2 | a0001 | c0014 | t0001 | g0037 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | MSL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03486 | hp2 | a0001 | c0007 | t0006 | g0027 | AFR | MSL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03516 | hp2 | a0001 | c0002 | t0003 | g0033 | AFR | ESN | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03540 | hp1 | a0003 | c0008 | t0002 | g0057 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03540 | hp2 | a0001 | c0003 | t0002 | g0015 | AFR | GWD | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03579 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | MSL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | BEB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18747 | hp1 | a0005 | c0010 | t0001 | g0119 | EAS | CHB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18747 | hp2 | a0014 | c0023 | t0002 | g0061 | EAS | CHB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18906 | hp1 | a0001 | c0002 | t0003 | g0005 | AFR | YRI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18906 | hp2 | a0001 | c0011 | t0001 | g0151 | AFR | YRI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18939 | hp1 | a0007 | c0026 | t0001 | g0054 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18980 | hp2 | a0009 | c0019 | t0001 | g0108 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18984 | hp2 | a0001 | c0015 | t0002 | g0035 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19030 | hp1 | a0001 | c0020 | t0002 | g0095 | AFR | LWK | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19030 | hp2 | a0010 | c0018 | t0001 | g0019 | AFR | LWK | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19043 | hp1 | a0001 | c0003 | t0002 | g0015 | AFR | LWK | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | LWK | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19063 | hp1 | a0005 | c0010 | t0001 | g0128 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19091 | hp1 | a0011 | c0017 | t0001 | g0009 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19240 | hp1 | a0004 | c0006 | t0003 | g0012 | AFR | YRI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | TSI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA20752 | hp2 | a0001 | c0001 | t0010 | g0141 | EUR | TSI | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | GIH | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA20905 | hp2 | a0006 | c0009 | t0001 | g0002 | SAS | GIH | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG06807 | hp1 | a0001 | c0005 | t0001 | g0135 | AFR | USA | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA20300 | hp1 | a0004 | c0006 | t0003 | g0012 | AFR | USA | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | USA | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
NA21309 | hp2 | a0001 | c0003 | t0002 | g0036 | AFR | LWK | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0004 | REF | REF | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0003 | g0034 | REF | REF | SRCAP_chr16_30694171_30746409 | SRCAP | chr16 | 30694171 | 30746409 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:30704071
|
C | T | 1 | a0007 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.62C>T | p.Ser21Leu | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/34 | 417/11724 | 62/9693 | 21/3230 | chr16 | 30704071 | ||
chr16:30711931
|
A | G | 1 | a0014 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.1589A>G | p.Glu530Gly | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 12/34 | 1944/11724 | 1589/9693 | 530/3230 | chr16 | 30711931 | ||
chr16:30720328
|
A | G | 1 | a0013 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.2984A>G | p.Asn995Ser | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 19/34 | 3339/11724 | 2984/9693 | 995/3230 | chr16 | 30720328 | ||
chr16:30720822
|
T | C | 1 | a0002 | 5 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(2): Show |
missense_variant | MODERATE | c.3097T>C | p.Ser1033Pro | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 20/34 | 3452/11724 | 3097/9693 | 1033/3230 | chr16 | 30720822 | ||
chr16:30720897
|
C | T | 1 | a0006 | 2 | HG02132.hp2 NA20905.hp2 |
missense_variant | MODERATE | c.3172C>T | p.Pro1058Ser | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 20/34 | 3527/11724 | 3172/9693 | 1058/3230 | chr16 | 30720897 | ||
chr16:30722256
|
C | G | 1 | a0005 | 2 | NA18747.hp1 NA19063.hp1 |
missense_variant | MODERATE | c.3676C>G | p.Leu1226Val | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 22/34 | 4031/11724 | 3676/9693 | 1226/3230 | chr16 | 30722256 | ||
chr16:30723613
|
A | G | 1 | a0012 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.4189A>G | p.Ile1397Val | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/34 | 4544/11724 | 4189/9693 | 1397/3230 | chr16 | 30723613 | ||
chr16:30724027
|
C | G | 1 | a0003 | 3 | HG01516.hp1 HG01517.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.4603C>G | p.Pro1535Ala | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/34 | 4958/11724 | 4603/9693 | 1535/3230 | chr16 | 30724027 | ||
chr16:30724955
|
C | G | 1 | a0008 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.5531C>G | p.Ser1844Cys | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/34 | 5886/11724 | 5531/9693 | 1844/3230 | chr16 | 30724955 | ||
chr16:30734539
|
C | T | 1 | a0009 | 1 | NA18980.hp2 | missense_variant | MODERATE | c.6653C>T | p.Ser2218Phe | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/34 | 7008/11724 | 6653/9693 | 2218/3230 | chr16 | 30734539 | ||
chr16:30737611
|
C | G | 1 | a0010 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.7571C>G | p.Ser2524Cys | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 7926/11724 | 7571/9693 | 2524/3230 | chr16 | 30737611 | ||
chr16:30738375
|
C | T | 1 | a0011 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.8335C>T | p.Pro2779Ser | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 8690/11724 | 8335/9693 | 2779/3230 | chr16 | 30738375 | ||
chr16:30738390
|
A | C | 1 | a0004 | 3 | HG01891.hp2 NA19240.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.8350A>C | p.Thr2784Pro | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 8705/11724 | 8350/9693 | 2784/3230 | chr16 | 30738390 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:30704141
|
C | T | 1 | a0001c0025 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.132C>T | p.Gly44Gly | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/34 | 487/11724 | 132/9693 | 44/3230 | chr16 | 30704141 | ||
chr16:30704198
|
C | G | 1 | a0001c0003 | 7 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
synonymous_variant | LOW | c.189C>G | p.Pro63Pro | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/34 | 544/11724 | 189/9693 | 63/3230 | chr16 | 30704198 | ||
chr16:30707194
|
C | T | 1 | a0001c0024 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.318C>T | p.Ile106Ile | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 5/34 | 673/11724 | 318/9693 | 106/3230 | chr16 | 30707194 | ||
chr16:30712318
|
T | C | 1 | a0001c0011 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.1872T>C | p.Ile624Ile | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 13/34 | 2227/11724 | 1872/9693 | 624/3230 | chr16 | 30712318 | ||
chr16:30712749
|
G | T | 23 | a0001c0001a0001c0003a0001c0005others(20): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
synonymous_variant | LOW | c.2064G>T | p.Arg688Arg | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 14/34 | 2419/11724 | 2064/9693 | 688/3230 | chr16 | 30712749 | ||
chr16:30713546
|
T | C | 1 | a0006c0009 | 2 | HG02132.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.2328T>C | p.Thr776Thr | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/34 | 2683/11724 | 2328/9693 | 776/3230 | chr16 | 30713546 | ||
chr16:30722279
|
G | A | 1 | a0001c0014 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.3699G>A | p.Pro1233Pro | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 22/34 | 4054/11724 | 3699/9693 | 1233/3230 | chr16 | 30722279 | ||
chr16:30723642
|
C | A | 25 | a0001c0001a0001c0003a0001c0005others(22): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
synonymous_variant | LOW | c.4218C>A | p.Ser1406Ser | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/34 | 4573/11724 | 4218/9693 | 1406/3230 | chr16 | 30723642 | ||
chr16:30725055
|
C | G | 2 | a0001c0020a0008c0021 | 2 | HG02145.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.5631C>G | p.Pro1877Pro | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/34 | 5986/11724 | 5631/9693 | 1877/3230 | chr16 | 30725055 | ||
chr16:30736286
|
T | C | 1 | a0001c0015 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.6816T>C | p.Asn2272Asn | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 32/34 | 7171/11724 | 6816/9693 | 2272/3230 | chr16 | 30736286 | ||
chr16:30736358
|
C | T | 1 | a0002c0013 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.6888C>T | p.Ser2296Ser | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 32/34 | 7243/11724 | 6888/9693 | 2296/3230 | chr16 | 30736358 | ||
chr16:30737303
|
C | A | 1 | a0001c0005 | 4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
synonymous_variant | LOW | c.7263C>A | p.Arg2421Arg | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 7618/11724 | 7263/9693 | 2421/3230 | chr16 | 30737303 | ||
chr16:30737579
|
G | T | 1 | a0001c0007 | 3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.7539G>T | p.Pro2513Pro | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 7894/11724 | 7539/9693 | 2513/3230 | chr16 | 30737579 | ||
chr16:30739152
|
T | C | 2 | a0001c0011a0001c0016 | 2 | HG01891.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.9112T>C | p.Leu3038Leu | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 9467/11724 | 9112/9693 | 3038/3230 | chr16 | 30739152 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:30700669
|
C | T | 1 | a0001c0001t0010 | 1 | NA20752.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-156C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/34 | chr16 | 30700669 | ||||||
chr16:30740075
|
CT | C | 15 | a0001c0001t0001a0001c0001t0005a0001c0005t0001others(12): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*358delT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 358 | INFO_REALIGN_3_PRIME | chr16 | 30740075 | ||||
chr16:30740075
|
CTT | C | 2 | a0001c0001t0004a0002c0004t0004 | 5 | HG00099.hp2 HG01071.hp2 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*357_*358delTT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 357 | INFO_REALIGN_3_PRIME | chr16 | 30740075 | ||||
chr16:30740481
|
G | A | 1 | a0001c0001t0007 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*748G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 748 | chr16 | 30740481 | |||||
chr16:30740752
|
C | T | 1 | a0001c0001t0009 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1019C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 1019 | chr16 | 30740752 | |||||
chr16:30740882
|
A | G | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(26): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*1149A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 1149 | chr16 | 30740882 | |||||
chr16:30740913
|
G | T | 1 | a0001c0001t0005 | 5 | HG02886.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1180G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 1180 | chr16 | 30740913 | |||||
chr16:30740955
|
A | G | 1 | a0001c0007t0006 | 3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1222A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 1222 | chr16 | 30740955 | |||||
chr16:30741328
|
A | G | 1 | a0004c0006t0008 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1595A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 34/34 | 1595 | chr16 | 30741328 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:30699705
|
T | A | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | HG00673.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-283-203T>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 1/33 | chr16 | 30699705 | ||||||
chr16:30699736
|
C | G | 1 | a0002c0013t0001g0155 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-283-172C>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 1/33 | chr16 | 30699736 | ||||||
chr16:30699758
|
C | A | 1 | a0002c0004t0001g0025 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-283-150C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 1/33 | chr16 | 30699758 | ||||||
chr16:30700245
|
T | C | 12 | a0001c0001t0001g0011a0001c0001t0004g0011a0001c0002t0003g0005others(9): Show | 15 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-210+264T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 2/33 | chr16 | 30700245 | ||||||
chr16:30700361
|
A | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-209-255A>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 2/33 | chr16 | 30700361 | ||||||
chr16:30700451
|
C | T | 1 | a0001c0003t0002g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-209-165C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 2/33 | chr16 | 30700451 | ||||||
chr16:30700467
|
G | C | 5 | a0001c0001t0001g0011a0001c0001t0004g0011a0001c0007t0006g0026others(2): Show | 5 | HG02280.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-209-149G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 2/33 | chr16 | 30700467 | ||||||
chr16:30700503
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0153 | 6 | HG02109.hp2 HG02809.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-209-113C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 2/33 | chr16 | 30700503 | ||||||
chr16:30700587
|
CT | C | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0039others(19): Show | 25 | HG01099.hp2 HG01109.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-209-14delT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 2/33 | INFO_REALIGN_3_PRIME | chr16 | 30700587 | |||||
chr16:30700925
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.54+47G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30700925 | ||||||
chr16:30700951
|
G | T | 7 | a0001c0002t0003g0005a0001c0002t0003g0029a0001c0002t0003g0032others(4): Show | 10 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.54+73G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30700951 | ||||||
chr16:30701000
|
C | A | 7 | a0001c0002t0003g0005a0001c0002t0003g0029a0001c0002t0003g0032others(4): Show | 10 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.54+122C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701000 | ||||||
chr16:30701084
|
C | T | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(5): Show | 10 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.54+206C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701084 | ||||||
chr16:30701154
|
A | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 6 | HG01928.hp1 HG01934.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+276A>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701154 | ||||||
chr16:30701157
|
C | A | 1 | a0001c0001t0002g0044 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.54+279C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701157 | ||||||
chr16:30701354
|
A | G | 1 | a0001c0001t0010g0141 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.54+476A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701354 | ||||||
chr16:30701636
|
C | CT | 4 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 5 | HG01081.hp1 HG01099.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+773dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30701636 | |||||
chr16:30701666
|
T | TTCTG | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(91): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.54+790_54+791insTG others(2): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30701666 | |||||
chr16:30701686
|
A | G | 2 | a0001c0011t0001g0151a0001c0016t0001g0152 | 2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.54+808A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701686 | ||||||
chr16:30701827
|
C | A | 5 | a0001c0003t0002g0015a0001c0003t0002g0036a0001c0003t0002g0103others(2): Show | 6 | HG01496.hp1 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+949C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701827 | ||||||
chr16:30701924
|
G | A | 1 | a0001c0001t0002g0045 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.54+1046G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701924 | ||||||
chr16:30701926
|
C | T | 1 | a0001c0001t0007g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.54+1048C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701926 | ||||||
chr16:30701952
|
C | CT | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0002t0003g0005others(2): Show | 7 | HG01109.hp2 HG02809.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+1088dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30701952 | |||||
chr16:30701952
|
C | CTTT | 3 | a0001c0001t0005g0010a0001c0001t0005g0149a0001c0001t0005g0150 | 5 | HG02886.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+1086_54+1088dup others(3): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30701952 | |||||
chr16:30701952
|
CT | C | 5 | a0001c0001t0001g0011a0001c0001t0004g0011a0001c0007t0006g0026others(2): Show | 5 | HG02280.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+1088delT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30701952 | |||||
chr16:30701979
|
G | C | 7 | a0001c0002t0003g0005a0001c0002t0003g0029a0001c0002t0003g0032others(4): Show | 10 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.54+1101G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30701979 | ||||||
chr16:30702057
|
A | G | 2 | a0004c0006t0003g0012a0004c0006t0008g0031 | 3 | HG01891.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.54+1179A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702057 | ||||||
chr16:30702101
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.54+1223G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702101 | ||||||
chr16:30702111
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.54+1233G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702111 | ||||||
chr16:30702377
|
C | T | 1 | a0004c0006t0008g0031 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.54+1499C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702377 | ||||||
chr16:30702568
|
TCCCTCCC others(6): Show |
T | 1 | a0001c0001t0002g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.55-1493_55-1481del others(13): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30702568 | |||||
chr16:30702571
|
C | T | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(5): Show | 10 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.55-1493C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702571 | ||||||
chr16:30702575
|
CTCCCTCC others(15): Show |
C | 3 | a0001c0001t0001g0043a0001c0001t0001g0139a0009c0019t0001g0108 | 3 | NA18939.hp2 NA18965.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.55-1475_55-1454del others(22): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30702575 | |||||
chr16:30702602
|
T | C | 4 | a0001c0002t0003g0005a0001c0002t0003g0029a0001c0002t0003g0032others(1): Show | 6 | HG01109.hp2 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-1462T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702602 | ||||||
chr16:30702702
|
G | A | 8 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0039others(5): Show | 10 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.55-1362G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702702 | ||||||
chr16:30702855
|
C | T | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(5): Show | 10 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.55-1209C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702855 | ||||||
chr16:30702884
|
T | A | 1 | a0012c0012t0003g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.55-1180T>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30702884 | ||||||
chr16:30703096
|
T | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(54): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.55-968T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30703096 | ||||||
chr16:30703149
|
C | CTA | 15 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0001g0132others(12): Show | 19 | HG01168.hp1 HG01169.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.55-897_55-896dupAT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30703149 | |||||
chr16:30703149
|
C | CTATA | 3 | a0001c0001t0001g0109a0001c0003t0002g0103a0001c0003t0002g0104 | 3 | HG01496.hp1 HG02145.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.55-899_55-896dupAT others(2): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30703149 | |||||
chr16:30703149
|
C | CTATATAT others(3): Show |
4 | a0001c0002t0003g0005a0001c0002t0003g0029a0004c0006t0003g0012others(1): Show | 7 | HG01891.hp2 HG02809.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.55-905_55-896dupAT others(8): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30703149 | |||||
chr16:30703149
|
C | CTATATAT others(5): Show |
3 | a0001c0001t0001g0011a0001c0001t0004g0011a0001c0002t0003g0033 | 3 | HG02896.hp2 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.55-907_55-896dupAT others(10): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30703149 | |||||
chr16:30703149
|
C | CTATATAT others(7): Show |
4 | a0001c0002t0003g0032a0001c0007t0006g0027a0001c0007t0006g0028others(1): Show | 4 | HG01109.hp2 HG01884.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-909_55-896dupAT others(12): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30703149 | |||||
chr16:30703149
|
C | CTATATAT others(9): Show |
1 | a0001c0007t0006g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.55-911_55-896dupAT others(14): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30703149 | |||||
chr16:30703172
|
T | C | 1 | a0001c0001t0002g0050 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.55-892T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30703172 | ||||||
chr16:30703460
|
C | G | 1 | a0001c0001t0001g0131 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.55-604C>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30703460 | ||||||
chr16:30703505
|
A | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0138 | 3 | HG01106.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.55-559A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30703505 | ||||||
chr16:30703507
|
A | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(91): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.55-557A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30703507 | ||||||
chr16:30703896
|
CA | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(73): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.55-161delA | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | INFO_REALIGN_3_PRIME | chr16 | 30703896 | |||||
chr16:30703955
|
A | C | 7 | a0001c0002t0003g0005a0001c0002t0003g0029a0001c0002t0003g0032others(4): Show | 10 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.55-109A>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 3/33 | chr16 | 30703955 | ||||||
chr16:30704319
|
C | T | 4 | a0001c0002t0003g0005a0001c0002t0003g0029a0001c0002t0003g0032others(1): Show | 6 | HG01109.hp2 HG02809.hp1 HG02965.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.306+4C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704319 | ||||||
chr16:30704344
|
C | T | 1 | a0001c0001t0010g0141 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.306+29C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704344 | ||||||
chr16:30704510
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.306+195A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704510 | ||||||
chr16:30704587
|
T | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(92): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.306+272T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704587 | ||||||
chr16:30704610
|
G | C | 1 | a0001c0001t0010g0141 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.306+295G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704610 | ||||||
chr16:30704649
|
G | A | 1 | a0001c0005t0001g0133 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.306+334G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704649 | ||||||
chr16:30704739
|
G | T | 1 | a0012c0012t0003g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.306+424G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704739 | ||||||
chr16:30704745
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.306+430G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30704745 | ||||||
chr16:30705236
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.306+921G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30705236 | ||||||
chr16:30705308
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.306+993G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30705308 | ||||||
chr16:30705318
|
G | C | 1 | a0012c0012t0003g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.306+1003G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30705318 | ||||||
chr16:30705429
|
C | T | 2 | a0003c0008t0002g0098a0003c0008t0002g0099 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.306+1114C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30705429 | ||||||
chr16:30705548
|
C | T | 2 | a0004c0006t0003g0012a0004c0006t0008g0031 | 3 | HG01891.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.306+1233C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30705548 | ||||||
chr16:30705707
|
G | GT | 12 | a0001c0001t0001g0097a0001c0001t0002g0096a0001c0001t0002g0145others(9): Show | 15 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.306+1405dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | INFO_REALIGN_3_PRIME | chr16 | 30705707 | |||||
chr16:30705765
|
G | A | 6 | a0001c0002t0003g0005a0001c0002t0003g0029a0001c0002t0003g0032others(3): Show | 9 | HG01109.hp2 HG01891.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-1418G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30705765 | ||||||
chr16:30705854
|
G | A | 1 | a0001c0014t0001g0037 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.307-1329G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30705854 | ||||||
chr16:30706030
|
T | G | 1 | a0001c0001t0002g0053 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.307-1153T>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706030 | ||||||
chr16:30706304
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0132 | 3 | HG02109.hp1 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.307-879A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706304 | ||||||
chr16:30706465
|
A | G | 6 | a0001c0003t0002g0015a0001c0003t0002g0036a0001c0003t0002g0103others(3): Show | 7 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-718A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706465 | ||||||
chr16:30706536
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.307-647A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706536 | ||||||
chr16:30706603
|
G | A | 4 | a0001c0005t0001g0133a0001c0005t0001g0134a0001c0005t0001g0135others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.307-580G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706603 | ||||||
chr16:30706609
|
C | T | 2 | a0001c0007t0006g0026a0001c0007t0006g0028 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.307-574C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706609 | ||||||
chr16:30706637
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0004g0011 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.307-546G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706637 | ||||||
chr16:30706667
|
C | A | 1 | a0007c0026t0001g0054 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.307-516C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30706667 | ||||||
chr16:30707176
|
T | C | 1 | a0001c0001t0002g0055 | 1 | NA18980.hp1 | splice_region_variant&intron_variant | LOW | c.307-7T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 4/33 | chr16 | 30707176 | ||||||
chr16:30707439
|
A | C | 1 | a0007c0026t0001g0054 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.492+71A>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 5/33 | chr16 | 30707439 | ||||||
chr16:30707552
|
C | T | 19 | a0001c0001t0001g0086a0001c0001t0001g0100a0001c0001t0002g0004others(16): Show | 22 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.493-20C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 5/33 | chr16 | 30707552 | ||||||
chr16:30707721
|
T | C | 1 | a0012c0012t0003g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.633+9T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30707721 | ||||||
chr16:30707736
|
G | A | 1 | a0004c0006t0008g0031 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.633+24G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30707736 | ||||||
chr16:30707986
|
C | T | 3 | a0001c0001t0002g0094a0001c0020t0002g0095a0008c0021t0002g0093 | 3 | HG01109.hp1 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.633+274C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30707986 | ||||||
chr16:30708077
|
C | A | 4 | a0001c0005t0001g0133a0001c0005t0001g0134a0001c0005t0001g0135others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.633+365C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30708077 | ||||||
chr16:30708503
|
C | T | 3 | a0001c0003t0002g0015a0001c0003t0002g0036a0001c0003t0002g0104 | 4 | HG02145.hp1 HG03540.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.633+791C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30708503 | ||||||
chr16:30708684
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0004g0111 | 2 | HG00099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.634-829G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30708684 | ||||||
chr16:30709055
|
G | A | 1 | a0001c0001t0002g0023 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.634-458G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30709055 | ||||||
chr16:30709279
|
A | T | 1 | a0001c0001t0001g0017 | 2 | HG00438.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.634-234A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30709279 | ||||||
chr16:30709451
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.634-62G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 6/33 | chr16 | 30709451 | ||||||
chr16:30710198
|
G | C | 3 | a0001c0007t0006g0026a0001c0007t0006g0027a0001c0007t0006g0028 | 3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1134+70G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 8/33 | chr16 | 30710198 | ||||||
chr16:30710284
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1134+156T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 8/33 | chr16 | 30710284 | ||||||
chr16:30710965
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1229-34A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 9/33 | chr16 | 30710965 | ||||||
chr16:30711492
|
G | A | 1 | a0001c0001t0002g0083 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1319-79G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 10/33 | chr16 | 30711492 | ||||||
chr16:30711775
|
G | A | 4 | a0001c0005t0001g0133a0001c0005t0001g0134a0001c0005t0001g0135others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1492+31G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 11/33 | chr16 | 30711775 | ||||||
chr16:30712605
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1994-74C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 13/33 | chr16 | 30712605 | ||||||
chr16:30712900
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2130+85C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 14/33 | chr16 | 30712900 | ||||||
chr16:30712901
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0004g0011 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2130+86T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 14/33 | chr16 | 30712901 | ||||||
chr16:30712920
|
A | T | 1 | a0007c0026t0001g0054 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2130+105A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 14/33 | chr16 | 30712920 | ||||||
chr16:30713075
|
C | T | 1 | a0007c0026t0001g0054 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2131-133C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 14/33 | chr16 | 30713075 | ||||||
chr16:30713813
|
G | T | 1 | a0005c0010t0001g0128 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2493+102G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30713813 | ||||||
chr16:30713831
|
G | A | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(5): Show | 10 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2493+120G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30713831 | ||||||
chr16:30713900
|
G | GT | 67 | a0001c0001t0001g0001a0001c0001t0001g0052a0001c0001t0001g0069others(64): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.2493+204dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr16 | 30713900 | |||||
chr16:30714034
|
A | T | 4 | a0001c0001t0002g0053a0001c0001t0002g0083a0001c0001t0002g0090others(1): Show | 4 | HG01255.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2493+323A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714034 | ||||||
chr16:30714064
|
A | AT | 17 | a0001c0001t0001g0043a0001c0001t0001g0127a0001c0001t0001g0136others(14): Show | 18 | HG01109.hp2 HG01169.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.2493+372dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr16 | 30714064 | |||||
chr16:30714133
|
T | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.2493+422T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714133 | ||||||
chr16:30714142
|
G | A | 1 | a0003c0008t0002g0057 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2493+431G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714142 | ||||||
chr16:30714169
|
A | G | 2 | a0001c0003t0002g0103a0001c0003t0002g0105 | 2 | HG01496.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2493+458A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714169 | ||||||
chr16:30714399
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0126a0011c0017t0001g0009 | 4 | NA18945.hp1 NA19081.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.2493+688C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714399 | ||||||
chr16:30714460
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2493+749C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714460 | ||||||
chr16:30714498
|
C | T | 2 | a0004c0006t0003g0012a0004c0006t0008g0031 | 3 | HG01891.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2493+787C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714498 | ||||||
chr16:30714507
|
C | CTTTTTTT others(3): Show |
17 | a0001c0001t0001g0126a0001c0001t0001g0146a0001c0001t0001g0147others(14): Show | 19 | HG01109.hp1 HG01168.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.2493+799_2493+808d others(12): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr16 | 30714507 | |||||
chr16:30714507
|
C | CTTTTTTT others(4): Show |
107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.2493+798_2493+808d others(13): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr16 | 30714507 | |||||
chr16:30714507
|
C | CTTTTTTT others(5): Show |
22 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0097others(19): Show | 23 | HG00673.hp2 HG00738.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.2493+797_2493+808d others(14): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr16 | 30714507 | |||||
chr16:30714507
|
C | CTTTTTTT others(6): Show |
3 | a0001c0003t0002g0015a0001c0003t0002g0104a0008c0021t0002g0093 | 4 | HG02145.hp1 HG02145.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2493+808_2493+809i others(15): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr16 | 30714507 | |||||
chr16:30714507
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0148 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2493+808_2493+809i others(16): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | INFO_REALIGN_3_PRIME | chr16 | 30714507 | |||||
chr16:30714593
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2493+882C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714593 | ||||||
chr16:30714655
|
G | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.2493+944G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714655 | ||||||
chr16:30714690
|
C | T | 1 | a0001c0005t0001g0133 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2493+979C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714690 | ||||||
chr16:30714786
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2493+1075T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714786 | ||||||
chr16:30714927
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(59): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2494-1139C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714927 | ||||||
chr16:30714937
|
T | G | 5 | a0001c0001t0001g0011a0001c0001t0004g0011a0001c0007t0006g0026others(2): Show | 5 | HG02280.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2494-1129T>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30714937 | ||||||
chr16:30715031
|
CA | C | 3 | a0001c0007t0006g0026a0001c0007t0006g0027a0001c0007t0006g0028 | 3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2494-1034delA | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715031 | ||||||
chr16:30715214
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2494-852A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715214 | ||||||
chr16:30715256
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2494-810G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715256 | ||||||
chr16:30715294
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0004g0011 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2494-772G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715294 | ||||||
chr16:30715579
|
A | G | 4 | a0001c0005t0001g0133a0001c0005t0001g0134a0001c0005t0001g0135others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2494-487A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715579 | ||||||
chr16:30715585
|
A | G | 2 | a0001c0001t0002g0087a0001c0001t0002g0088 | 2 | HG02735.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2494-481A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715585 | ||||||
chr16:30715646
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2494-420G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715646 | ||||||
chr16:30715722
|
C | T | 1 | a0004c0006t0008g0031 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2494-344C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715722 | ||||||
chr16:30715906
|
C | T | 1 | a0001c0003t0002g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2494-160C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 16/33 | chr16 | 30715906 | ||||||
chr16:30716532
|
C | G | 2 | a0001c0001t0001g0052a0001c0001t0002g0046 | 2 | HG01081.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2817+53C>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30716532 | ||||||
chr16:30716560
|
T | G | 2 | a0001c0001t0001g0011a0001c0001t0004g0011 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2817+81T>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30716560 | ||||||
chr16:30716713
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2817+234C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30716713 | ||||||
chr16:30717063
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0042 | 3 | HG01081.hp1 HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.2817+584C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30717063 | ||||||
chr16:30717103
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2817+624C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30717103 | ||||||
chr16:30717123
|
T | A | 1 | a0001c0007t0006g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2817+644T>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30717123 | ||||||
chr16:30717561
|
C | T | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(5): Show | 10 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2817+1082C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30717561 | ||||||
chr16:30717610
|
C | CT | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(99): Show | 127 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.2817+1152dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | INFO_REALIGN_3_PRIME | chr16 | 30717610 | |||||
chr16:30717610
|
C | CTT | 49 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0021others(46): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.2817+1151_2817+115 others(6): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | INFO_REALIGN_3_PRIME | chr16 | 30717610 | |||||
chr16:30717610
|
C | CTTT | 4 | a0001c0001t0002g0006a0001c0001t0002g0081a0001c0001t0002g0082others(1): Show | 6 | HG01175.hp1 HG01192.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.2817+1150_2817+115 others(7): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | INFO_REALIGN_3_PRIME | chr16 | 30717610 | |||||
chr16:30718302
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0004g0011a0001c0007t0006g0026others(2): Show | 5 | HG02280.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2817+1823G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30718302 | ||||||
chr16:30718325
|
C | T | 6 | a0001c0001t0001g0097a0001c0001t0002g0014a0001c0001t0002g0074others(3): Show | 7 | HG02040.hp1 HG02129.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.2818-1837C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30718325 | ||||||
chr16:30718418
|
C | G | 2 | a0001c0001t0002g0072a0001c0001t0002g0073 | 2 | HG00735.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.2818-1744C>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30718418 | ||||||
chr16:30718475
|
CT | C | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(5): Show | 10 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2818-1671delT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | INFO_REALIGN_3_PRIME | chr16 | 30718475 | |||||
chr16:30718617
|
G | A | 1 | a0001c0001t0002g0078 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2818-1545G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30718617 | ||||||
chr16:30718953
|
A | G | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(75): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.2818-1209A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30718953 | ||||||
chr16:30718997
|
A | T | 1 | a0001c0001t0001g0040 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2818-1165A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30718997 | ||||||
chr16:30718999
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2818-1163C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30718999 | ||||||
chr16:30719217
|
T | TTTA | 67 | a0001c0001t0001g0001a0001c0001t0001g0052a0001c0001t0001g0069others(64): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.2818-943_2818-942i others(5): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | INFO_REALIGN_3_PRIME | chr16 | 30719217 | |||||
chr16:30719222
|
A | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0052a0001c0001t0001g0069others(64): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.2818-940A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719222 | ||||||
chr16:30719222
|
AT | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(88): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2818-929delT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | INFO_REALIGN_3_PRIME | chr16 | 30719222 | |||||
chr16:30719223
|
T | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0052a0001c0001t0001g0069others(64): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.2818-939T>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719223 | ||||||
chr16:30719302
|
G | A | 1 | a0001c0003t0002g0105 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2818-860G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719302 | ||||||
chr16:30719330
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2818-832T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719330 | ||||||
chr16:30719358
|
G | A | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(59): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2818-804G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719358 | ||||||
chr16:30719572
|
G | A | 1 | a0014c0023t0002g0061 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2818-590G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719572 | ||||||
chr16:30719666
|
A | G | 1 | a0001c0007t0006g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2818-496A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719666 | ||||||
chr16:30719870
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2818-292T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719870 | ||||||
chr16:30719951
|
G | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.2818-211G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 18/33 | chr16 | 30719951 | ||||||
chr16:30720518
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2987+187G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 19/33 | chr16 | 30720518 | ||||||
chr16:30721085
|
C | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.3254-104C>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 20/33 | chr16 | 30721085 | ||||||
chr16:30721564
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0004g0013 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3541+88A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 21/33 | chr16 | 30721564 | ||||||
chr16:30721591
|
C | T | 1 | a0001c0001t0004g0111 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3541+115C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 21/33 | chr16 | 30721591 | ||||||
chr16:30721731
|
T | G | 1 | a0001c0001t0002g0081 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3541+255T>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 21/33 | chr16 | 30721731 | ||||||
chr16:30722088
|
G | T | 3 | a0001c0005t0001g0133a0001c0005t0001g0135a0001c0005t0001g0137 | 3 | HG02055.hp1 HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3542-34G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 21/33 | chr16 | 30722088 | ||||||
chr16:30722783
|
G | T | 1 | a0001c0001t0009g0077 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3892+35G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 23/33 | chr16 | 30722783 | ||||||
chr16:30722864
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3893-99G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 23/33 | chr16 | 30722864 | ||||||
chr16:30723324
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4159+95A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 24/33 | chr16 | 30723324 | ||||||
chr16:30723402
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4159+173T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 24/33 | chr16 | 30723402 | ||||||
chr16:30725169
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5658+87A>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30725169 | ||||||
chr16:30725386
|
T | G | 3 | a0001c0007t0006g0026a0001c0007t0006g0027a0001c0007t0006g0028 | 3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5658+304T>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30725386 | ||||||
chr16:30725421
|
A | G | 6 | a0001c0003t0002g0015a0001c0003t0002g0036a0001c0003t0002g0103others(3): Show | 7 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5658+339A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30725421 | ||||||
chr16:30725658
|
T | C | 1 | a0001c0001t0002g0065 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.5658+576T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30725658 | ||||||
chr16:30725802
|
T | A | 2 | a0001c0001t0001g0121a0001c0024t0001g0112 | 2 | HG02738.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.5658+720T>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30725802 | ||||||
chr16:30725993
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5658+911C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30725993 | ||||||
chr16:30726046
|
T | G | 1 | a0001c0001t0002g0062 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.5658+964T>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30726046 | ||||||
chr16:30726185
|
T | C | 2 | a0001c0001t0002g0023a0001c0001t0002g0024 | 2 | HG00673.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.5658+1103T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30726185 | ||||||
chr16:30726196
|
C | T | 1 | a0001c0001t0002g0071 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5658+1114C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30726196 | ||||||
chr16:30726522
|
CT | C | 5 | a0001c0001t0001g0136a0001c0001t0002g0066a0001c0001t0002g0090others(2): Show | 5 | HG01256.hp1 HG01517.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.5658+1456delT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | INFO_REALIGN_3_PRIME | chr16 | 30726522 | |||||
chr16:30726584
|
G | A | 19 | a0001c0001t0001g0086a0001c0001t0001g0100a0001c0001t0002g0004others(16): Show | 22 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.5658+1502G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30726584 | ||||||
chr16:30726984
|
G | A | 4 | a0001c0005t0001g0133a0001c0005t0001g0134a0001c0005t0001g0135others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.5658+1902G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30726984 | ||||||
chr16:30727140
|
A | T | 1 | a0001c0001t0001g0118 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5659-1826A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30727140 | ||||||
chr16:30727512
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.5659-1454A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30727512 | ||||||
chr16:30727708
|
C | T | 3 | a0001c0007t0006g0026a0001c0007t0006g0027a0001c0007t0006g0028 | 3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5659-1258C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30727708 | ||||||
chr16:30727844
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5659-1122G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30727844 | ||||||
chr16:30728170
|
G | A | 3 | a0001c0007t0006g0026a0001c0007t0006g0027a0001c0007t0006g0028 | 3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5659-796G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30728170 | ||||||
chr16:30728598
|
T | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(59): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.5659-368T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30728598 | ||||||
chr16:30728610
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5659-356A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30728610 | ||||||
chr16:30728743
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5659-223T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30728743 | ||||||
chr16:30728821
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.5659-145T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 25/33 | chr16 | 30728821 | ||||||
chr16:30729737
|
G | A | 4 | a0001c0005t0001g0133a0001c0005t0001g0134a0001c0005t0001g0135others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.6127+165G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30729737 | ||||||
chr16:30729918
|
C | T | 2 | a0004c0006t0003g0012a0004c0006t0008g0031 | 3 | HG01891.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6127+346C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30729918 | ||||||
chr16:30730338
|
C | CGCTTAAA others(14): Show |
155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.6127+766_6127+767i others(23): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30730338 | ||||||
chr16:30730353
|
G | A | 1 | a0001c0003t0002g0103 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.6127+781G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30730353 | ||||||
chr16:30730639
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6127+1067T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30730639 | ||||||
chr16:30730642
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6127+1070G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30730642 | ||||||
chr16:30730729
|
C | CT | 9 | a0001c0001t0001g0117a0001c0001t0001g0146a0001c0001t0001g0147others(6): Show | 11 | HG01891.hp1 HG02280.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.6127+1171dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | INFO_REALIGN_3_PRIME | chr16 | 30730729 | |||||
chr16:30730928
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6127+1356A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30730928 | ||||||
chr16:30730946
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.6127+1374A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30730946 | ||||||
chr16:30731216
|
T | C | 1 | a0001c0007t0006g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6127+1644T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30731216 | ||||||
chr16:30731453
|
C | T | 3 | a0001c0007t0006g0026a0001c0007t0006g0027a0001c0007t0006g0028 | 3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.6128-1827C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30731453 | ||||||
chr16:30731750
|
C | T | 4 | a0001c0005t0001g0133a0001c0005t0001g0134a0001c0005t0001g0135others(1): Show | 4 | HG02055.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.6128-1530C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30731750 | ||||||
chr16:30732201
|
C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0052a0001c0001t0001g0069others(65): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.6128-1079C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30732201 | ||||||
chr16:30732236
|
G | A | 2 | a0004c0006t0003g0012a0004c0006t0008g0031 | 3 | HG01891.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6128-1044G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30732236 | ||||||
chr16:30732392
|
C | T | 3 | a0001c0007t0006g0026a0001c0007t0006g0027a0001c0007t0006g0028 | 3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.6128-888C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30732392 | ||||||
chr16:30732705
|
T | C | 3 | a0001c0007t0006g0026a0001c0007t0006g0027a0001c0007t0006g0028 | 3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.6128-575T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30732705 | ||||||
chr16:30732870
|
T | G | 1 | a0001c0001t0010g0141 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.6128-410T>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30732870 | ||||||
chr16:30732879
|
C | T | 2 | a0001c0001t0002g0075a0001c0001t0002g0076 | 2 | HG02129.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.6128-401C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30732879 | ||||||
chr16:30732899
|
C | A | 1 | a0001c0001t0002g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.6128-381C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30732899 | ||||||
chr16:30733156
|
T | C | 6 | a0001c0007t0006g0026a0001c0007t0006g0027a0001c0007t0006g0028others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.6128-124T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 27/33 | chr16 | 30733156 | ||||||
chr16:30733505
|
C | T | 4 | a0001c0001t0001g0070a0001c0001t0002g0072a0001c0001t0002g0073others(1): Show | 4 | HG00323.hp2 HG00735.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.6297+56C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 28/33 | chr16 | 30733505 | ||||||
chr16:30733516
|
G | T | 1 | a0001c0003t0002g0104 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6297+67G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 28/33 | chr16 | 30733516 | ||||||
chr16:30733886
|
C | A | 2 | a0001c0001t0001g0011a0001c0001t0004g0011 | 2 | HG02896.hp2 HG02897.hp2 |
splice_region_variant&intron_variant | LOW | c.6495-8C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 29/33 | chr16 | 30733886 | ||||||
chr16:30734141
|
G | T | 2 | a0004c0006t0003g0012a0004c0006t0008g0031 | 3 | HG01891.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6609+133G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 30/33 | chr16 | 30734141 | ||||||
chr16:30734215
|
C | T | 1 | a0012c0012t0003g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.6609+207C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 30/33 | chr16 | 30734215 | ||||||
chr16:30734655
|
C | T | 4 | a0001c0001t0001g0070a0001c0001t0002g0072a0001c0001t0002g0073others(1): Show | 4 | HG00323.hp2 HG00735.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.6729+40C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30734655 | ||||||
chr16:30734705
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.6729+90A>G | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30734705 | ||||||
chr16:30734848
|
T | C | 2 | a0001c0001t0002g0058a0001c0015t0002g0035 | 2 | HG00438.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.6729+233T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30734848 | ||||||
chr16:30735136
|
A | ATTTTTTT others(5): Show |
2 | a0001c0007t0006g0026a0001c0007t0006g0028 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.6729+538_6729+549d others(14): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | |||||
chr16:30735136
|
A | ATTTTTTT others(7): Show |
1 | a0001c0007t0006g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6729+536_6729+549d others(16): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | |||||
chr16:30735136
|
AT | A | 7 | a0001c0001t0001g0109a0001c0003t0002g0015a0001c0003t0002g0104others(4): Show | 9 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.6729+549delT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | |||||
chr16:30735136
|
ATTTT | A | 6 | a0001c0001t0001g0120a0001c0001t0001g0127a0001c0001t0001g0139others(3): Show | 6 | HG01175.hp2 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.6729+546_6729+549d others(6): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | |||||
chr16:30735136
|
ATTTTT | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(64): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.6729+545_6729+549d others(7): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | |||||
chr16:30735136
|
ATTTTTT | A | 4 | a0001c0001t0005g0010a0001c0001t0005g0149a0005c0010t0001g0119others(1): Show | 6 | HG02886.hp2 HG03139.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.6729+544_6729+549d others(8): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | |||||
chr16:30735136
|
ATTTTTTT others(3): Show |
A | 4 | a0001c0001t0001g0086a0001c0001t0002g0064a0001c0001t0002g0068others(1): Show | 4 | HG00408.hp2 HG01496.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.6729+540_6729+549d others(12): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | |||||
chr16:30735136
|
ATTTTTTT others(4): Show |
A | 61 | a0001c0001t0001g0001a0001c0001t0001g0052a0001c0001t0001g0069others(58): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.6729+539_6729+549d others(13): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | |||||
chr16:30735136
|
ATTTTTTT others(5): Show |
A | 3 | a0001c0001t0001g0097a0001c0001t0002g0066a0001c0001t0002g0082 | 3 | HG01517.hp2 NA18995.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.6729+538_6729+549d others(14): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735136 | |||||
chr16:30735171
|
G | A | 1 | a0001c0007t0006g0027 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6729+556G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735171 | ||||||
chr16:30735177
|
C | A | 1 | a0001c0001t0001g0153 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6729+562C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735177 | ||||||
chr16:30735240
|
G | A | 2 | a0001c0011t0001g0151a0001c0016t0001g0152 | 2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6729+625G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735240 | ||||||
chr16:30735357
|
G | A | 2 | a0001c0007t0006g0026a0001c0007t0006g0028 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.6729+742G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735357 | ||||||
chr16:30735476
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.6730-724C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735476 | ||||||
chr16:30735501
|
C | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(75): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.6730-699C>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735501 | ||||||
chr16:30735567
|
C | CT | 8 | a0001c0001t0001g0097a0001c0001t0001g0100a0001c0001t0002g0072others(5): Show | 9 | HG00323.hp1 HG01256.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.6730-611dupT | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735567 | |||||
chr16:30735567
|
C | CTT | 75 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0052others(72): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.6730-612_6730-611d others(4): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735567 | |||||
chr16:30735567
|
C | CTTT | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(63): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.6730-613_6730-611d others(5): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735567 | |||||
chr16:30735567
|
C | CTTTT | 5 | a0001c0001t0001g0042a0001c0001t0001g0110a0001c0001t0001g0115others(2): Show | 5 | HG01099.hp2 HG01346.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.6730-614_6730-611d others(6): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735567 | |||||
chr16:30735567
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6730-633C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735567 | ||||||
chr16:30735567
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.6730-620_6730-611d others(12): Show |
SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | INFO_REALIGN_3_PRIME | chr16 | 30735567 | |||||
chr16:30735605
|
G | T | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6730-595G>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735605 | ||||||
chr16:30735631
|
A | T | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6730-569A>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735631 | ||||||
chr16:30735649
|
C | T | 3 | a0001c0007t0006g0026a0001c0007t0006g0027a0001c0007t0006g0028 | 3 | HG02280.hp2 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.6730-551C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735649 | ||||||
chr16:30735826
|
G | A | 4 | a0001c0001t0001g0114a0001c0001t0001g0123a0005c0010t0001g0119others(1): Show | 4 | HG00673.hp2 NA18747.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.6730-374G>A | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735826 | ||||||
chr16:30735870
|
C | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(75): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.6730-330C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30735870 | ||||||
chr16:30736109
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0132a0001c0003t0002g0154 | 4 | HG01884.hp2 HG02109.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.6730-91C>T | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30736109 | ||||||
chr16:30736126
|
T | C | 1 | a0001c0001t0002g0085 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.6730-74T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 31/33 | chr16 | 30736126 | ||||||
chr16:30736838
|
A | C | 6 | a0001c0003t0002g0015a0001c0003t0002g0036a0001c0003t0002g0103others(3): Show | 7 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.7009-211A>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 33/33 | chr16 | 30736838 | ||||||
chr16:30736862
|
G | C | 3 | a0003c0008t0002g0057a0003c0008t0002g0098a0003c0008t0002g0099 | 3 | HG01516.hp1 HG01517.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.7009-187G>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 33/33 | chr16 | 30736862 | ||||||
chr16:30737000
|
T | C | 1 | a0001c0003t0002g0105 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.7009-49T>C | SRCAP | ENSG00000080603.17 | transcript | ENST00000262518.9 | protein_coding | 33/33 | chr16 | 30737000 |