geneid | 6396 |
---|---|
ensemblid | ENSG00000157020.18 |
hgncid | 10697 |
symbol | SEC13 |
name | SEC13 homolog, nuclear pore and COPII coat complex component |
refseq_nuc | NM_183352.3 |
refseq_prot | NP_899195.1 |
ensembl_nuc | ENST00000350697.8 |
ensembl_prot | ENSP00000312122.4 |
mane_status | MANE Select |
chr | chr3 |
start | 10300931 |
end | 10321112 |
strand | - |
ver | v1.2 |
region | chr3:10300931-10321112 |
region5000 | chr3:10295931-10326112 |
regionname0 | SEC13_chr3_10300931_10321112 |
regionname5000 | SEC13_chr3_10295931_10326112 |
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 | 322 | 378 | 96 | 61 | 159 | 10 | 50 | 111 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
a0002 | 0/0 | 322 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
a0003 | 0/0 | 322 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 969 | 370 | 89 | 60 | 159 | 10 | 50 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
c0002 | 0/0 | 969 | 7 | 7 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
c0003 | 0/0 | 969 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
c0004 | 0/0 | 969 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
c0005 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 391 | 317 | 71 | 45 | 156 | 7 | 37 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
t0002 | 1/0 | 391 | 60 | 23 | 17 | 3 | 3 | 13 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
t0003 | 0/0 | 391 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
t0004 | 0/0 | 391 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
t0005 | 0/0 | 391 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
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 | 22 | 0 | 11 | 8 | 1 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0002 | 0/0 | 17 | 0 | 3 | 11 | 2 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0003 | 0/0 | 14 | 0 | 1 | 12 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0004 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0005 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0007 | 0/0 | 5 | 0 | 0 | 2 | 2 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0012 | 0/0 | 4 | 2 | 0 | 0 | 1 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0013 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0017 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0019 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0020 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 969 | 370 | 89 | 60 | 159 | 10 | 50 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
a0001c0002 | 0/0 | 969 | 7 | 7 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
a0001c0004 | 0/0 | 969 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
a0002c0005 | 0/0 | 969 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
a0003c0003 | 0/0 | 969 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1359 | 316 | 71 | 45 | 155 | 7 | 37 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
a0001c0001t0002 | 1/0 | 1359 | 51 | 16 | 15 | 3 | 3 | 13 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
a0001c0001t0003 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
a0001c0001t0004 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
a0001c0001t0005 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
a0001c0002t0002 | 0/0 | 1359 | 7 | 7 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
a0001c0004t0002 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
a0002c0005t0001 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
a0003c0003t0002 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | copy fasta | chr3 | 10295931 | 10326112 |
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 | 22 | 0 | 11 | 8 | 1 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0002 | 0/0 | 17 | 0 | 3 | 11 | 2 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0003 | 0/0 | 14 | 0 | 1 | 12 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0004 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 2 | 2 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0012 | 0/0 | 4 | 2 | 0 | 0 | 1 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0019 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0013 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0001c0004t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0002c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
a0003c0003t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | GBR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | FIN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01106 | hp1 | a0003 | c0003 | t0002 | g0233 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0020 | EUR | IBS | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01981 | hp1 | a0001 | c0004 | t0002 | g0050 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0062 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CDX | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0095 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0122 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0116 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0117 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0121 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | BEB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0098 | AFR | YRI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | YRI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18984 | hp1 | a0002 | c0005 | t0001 | g0144 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ASW | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ASW | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | GIH | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | GIH | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0115 | AFR | MSL | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | USA | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | USA | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | USA | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | USA | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0019 | REF | REF | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0079 | REF | REF | SEC13_chr3_10295931_10326112 | SEC13 | chr3 | 10295931 | 10326112 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:10305050
|
T | C | 1 | a0002 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.691A>G | p.Ile231Val | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/9 | 751/1359 | 691/969 | 231/322 | chr3 | 10305050 | ||
chr3:10312066
|
C | T | 1 | a0003 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.349G>A | p.Gly117Ser | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/9 | 409/1359 | 349/969 | 117/322 | chr3 | 10312066 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:10301303
|
G | A | 1 | a0001c0004 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.927C>T | p.Ser309Ser | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 9/9 | 987/1359 | 927/969 | 309/322 | chr3 | 10301303 | ||
chr3:10312595
|
C | T | 1 | a0001c0002 | 7 | HG02630.hp1 HG02630.hp2 HG02809.hp1 others(4): Show |
synonymous_variant | LOW | c.300G>A | p.Ala100Ala | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 4/9 | 360/1359 | 300/969 | 100/322 | chr3 | 10312595 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:10301061
|
A | C | 1 | a0001c0001t0005 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 9/9 | 200 | chr3 | 10301061 | |||||
chr3:10301192
|
C | T | 5 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(2): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*69G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 9/9 | 69 | chr3 | 10301192 | |||||
chr3:10301206
|
C | G | 1 | a0001c0001t0004 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 9/9 | 55 | chr3 | 10301206 | |||||
chr3:10321104
|
C | T | 1 | a0001c0001t0003 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-52G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/9 | 52 | chr3 | 10321104 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:10301409
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.856-35G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301409 | ||||||
chr3:10301520
|
C | A | 3 | a0001c0001t0001g0091a0001c0001t0001g0099a0001c0001t0001g0126 | 3 | NA18979.hp2 NA18985.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.856-146G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301520 | ||||||
chr3:10301560
|
G | A | 40 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(37): Show | 57 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.856-186C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301560 | ||||||
chr3:10301588
|
T | C | 2 | a0001c0001t0002g0038a0001c0002t0002g0117 | 3 | HG02622.hp1 HG02723.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.856-214A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301588 | ||||||
chr3:10301638
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG00673.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.856-264C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301638 | ||||||
chr3:10301728
|
T | C | 5 | a0001c0001t0001g0010a0001c0001t0001g0084a0001c0001t0001g0152others(2): Show | 9 | HG00438.hp1 HG02015.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-354A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301728 | ||||||
chr3:10301926
|
A | AAATT | 11 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0037others(8): Show | 15 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.856-556_856-553dup others(4): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301926 | ||||||
chr3:10301943
|
T | TA | 10 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0047others(7): Show | 27 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.856-570dupT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301943 | ||||||
chr3:10301992
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.856-618T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10301992 | ||||||
chr3:10302035
|
A | G | 15 | a0001c0001t0002g0027a0001c0001t0002g0072a0001c0001t0002g0078others(12): Show | 16 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.856-661T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302035 | ||||||
chr3:10302153
|
G | A | 10 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0047others(7): Show | 27 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.856-779C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302153 | ||||||
chr3:10302173
|
G | A | 3 | a0001c0001t0001g0212a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02055.hp1 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.856-799C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302173 | ||||||
chr3:10302193
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0067a0001c0001t0001g0073 | 4 | HG01891.hp1 HG02258.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-819C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302193 | ||||||
chr3:10302427
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(140): Show | 244 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.856-1053C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302427 | ||||||
chr3:10302495
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.856-1121C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302495 | ||||||
chr3:10302646
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.856-1272C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302646 | ||||||
chr3:10302743
|
A | G | 18 | a0001c0001t0001g0223a0001c0001t0002g0027a0001c0001t0002g0038others(15): Show | 20 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.855+1283T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302743 | ||||||
chr3:10302824
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.855+1202C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302824 | ||||||
chr3:10302900
|
G | A | 15 | a0001c0001t0002g0027a0001c0001t0002g0072a0001c0001t0002g0078others(12): Show | 16 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.855+1126C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302900 | ||||||
chr3:10302962
|
T | TTAGA | 15 | a0001c0001t0002g0027a0001c0001t0002g0072a0001c0001t0002g0078others(12): Show | 16 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.855+1060_855+1063d others(6): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10302962 | ||||||
chr3:10303005
|
G | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(45): Show | 72 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.855+1021C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303005 | ||||||
chr3:10303038
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.855+988T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303038 | ||||||
chr3:10303159
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0143 | 3 | HG01070.hp1 HG01071.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.855+867C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303159 | ||||||
chr3:10303173
|
C | T | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0244others(8): Show | 13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.855+853G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303173 | ||||||
chr3:10303267
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.855+759G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303267 | ||||||
chr3:10303324
|
C | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0141a0001c0001t0001g0142others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.855+702G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303324 | ||||||
chr3:10303447
|
G | GACCTTGG others(29): Show |
1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.855+543_855+578dup others(36): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303447 | ||||||
chr3:10303496
|
G | T | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.855+530C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303496 | ||||||
chr3:10303843
|
G | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(50): Show | 79 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.855+183C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303843 | ||||||
chr3:10303972
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.855+54G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303972 | ||||||
chr3:10303973
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.855+53C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 8/8 | chr3 | 10303973 | ||||||
chr3:10304184
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0216others(1): Show | 6 | HG01884.hp1 HG02145.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.709-12G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304184 | ||||||
chr3:10304237
|
C | T | 38 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(35): Show | 55 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.709-65G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304237 | ||||||
chr3:10304379
|
C | T | 12 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0026others(9): Show | 18 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.709-207G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304379 | ||||||
chr3:10304386
|
C | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0141a0001c0001t0001g0142others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.709-214G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304386 | ||||||
chr3:10304387
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.709-215C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304387 | ||||||
chr3:10304737
|
G | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(50): Show | 79 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.708+296C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304737 | ||||||
chr3:10304786
|
T | A | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.708+247A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304786 | ||||||
chr3:10304889
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.708+144T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304889 | ||||||
chr3:10304993
|
G | A | 1 | a0001c0001t0002g0228 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.708+40C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10304993 | ||||||
chr3:10305030
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG01358.hp1 | splice_region_variant&intron_variant | LOW | c.708+3C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 7/8 | chr3 | 10305030 | ||||||
chr3:10305193
|
C | T | 13 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0089others(10): Show | 15 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.585-37G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305193 | ||||||
chr3:10305311
|
G | GT | 16 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0035others(13): Show | 22 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.585-156dupA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305311 | ||||||
chr3:10305312
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.585-156A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305312 | ||||||
chr3:10305312
|
T | TA | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(139): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.585-157dupT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305312 | ||||||
chr3:10305312
|
T | TAA | 8 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(5): Show | 8 | HG00673.hp2 HG01993.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.585-158_585-157dup others(2): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305312 | ||||||
chr3:10305321
|
C | A | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.585-165G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305321 | ||||||
chr3:10305459
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.584+100C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305459 | ||||||
chr3:10305460
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.584+99T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 6/8 | chr3 | 10305460 | ||||||
chr3:10305829
|
G | A | 1 | a0001c0001t0004g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.451-137C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10305829 | ||||||
chr3:10305862
|
CAACAGT | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(49): Show | 78 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.451-176_451-171del others(6): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10305862 | ||||||
chr3:10305892
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG00673.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-200C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10305892 | ||||||
chr3:10306001
|
A | G | 2 | a0001c0001t0002g0096a0001c0001t0002g0118 | 2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.451-309T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306001 | ||||||
chr3:10306023
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.451-331C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306023 | ||||||
chr3:10306038
|
C | A | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.451-346G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306038 | ||||||
chr3:10306126
|
C | T | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0244others(8): Show | 13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-434G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306126 | ||||||
chr3:10306159
|
A | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(50): Show | 79 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.451-467T>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306159 | ||||||
chr3:10306196
|
G | T | 8 | a0001c0001t0001g0030a0001c0001t0001g0141a0001c0001t0001g0142others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.451-504C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306196 | ||||||
chr3:10306286
|
T | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0084a0001c0001t0001g0152others(2): Show | 9 | HG00438.hp1 HG02015.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.451-594A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306286 | ||||||
chr3:10306393
|
T | G | 1 | a0001c0001t0001g0031 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.451-701A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306393 | ||||||
chr3:10306432
|
T | G | 15 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0035others(12): Show | 21 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.451-740A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306432 | ||||||
chr3:10306435
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.451-743G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306435 | ||||||
chr3:10306437
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0156 | 2 | HG01071.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.451-745G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306437 | ||||||
chr3:10306501
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.451-809A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306501 | ||||||
chr3:10306535
|
C | T | 8 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0215others(5): Show | 11 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.451-843G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306535 | ||||||
chr3:10306551
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.451-859A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306551 | ||||||
chr3:10306682
|
T | TA | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0216 | 5 | HG01884.hp1 HG02145.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-991dupT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306682 | ||||||
chr3:10306746
|
C | T | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0244others(8): Show | 13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-1054G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306746 | ||||||
chr3:10306781
|
T | C | 1 | a0001c0001t0001g0017 | 3 | HG00741.hp2 HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.451-1089A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306781 | ||||||
chr3:10306824
|
T | C | 1 | a0001c0001t0002g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.451-1132A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306824 | ||||||
chr3:10306849
|
G | A | 15 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0035others(12): Show | 21 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.451-1157C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306849 | ||||||
chr3:10306934
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.451-1242G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10306934 | ||||||
chr3:10307053
|
A | AT | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 143 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.451-1362dupA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307053 | ||||||
chr3:10307065
|
A | T | 45 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(42): Show | 64 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.451-1373T>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307065 | ||||||
chr3:10307066
|
A | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0213others(1): Show | 6 | HG01884.hp1 HG02145.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-1374T>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307066 | ||||||
chr3:10307090
|
C | G | 1 | a0001c0001t0004g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.451-1398G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307090 | ||||||
chr3:10307146
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.451-1454C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307146 | ||||||
chr3:10307212
|
CT | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(208): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.451-1521delA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307212 | ||||||
chr3:10307310
|
GTGATTC | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 143 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.451-1624_451-1619d others(8): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307310 | ||||||
chr3:10307322
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.451-1630G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307322 | ||||||
chr3:10307331
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.451-1639G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307331 | ||||||
chr3:10307333
|
C | T | 38 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(35): Show | 55 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.451-1641G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307333 | ||||||
chr3:10307366
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.451-1674C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307366 | ||||||
chr3:10307478
|
T | G | 1 | a0001c0001t0001g0173 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.451-1786A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307478 | ||||||
chr3:10307493
|
A | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0084others(13): Show | 27 | HG00438.hp1 HG02015.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.451-1801T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307493 | ||||||
chr3:10307494
|
T | G | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG01071.hp1 HG01175.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-1802A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307494 | ||||||
chr3:10307531
|
AG | A | 39 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(36): Show | 56 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.451-1840delC | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307531 | ||||||
chr3:10307613
|
C | T | 1 | a0001c0001t0001g0018 | 3 | HG02615.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.451-1921G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307613 | ||||||
chr3:10307631
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.451-1939A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307631 | ||||||
chr3:10307688
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.451-1996G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307688 | ||||||
chr3:10307690
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(66): Show | 131 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.451-1998C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307690 | ||||||
chr3:10307762
|
C | T | 38 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(35): Show | 55 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.451-2070G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307762 | ||||||
chr3:10307822
|
G | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0203 | 2 | NA18947.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.451-2130C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307822 | ||||||
chr3:10307873
|
C | G | 1 | a0001c0001t0002g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.451-2181G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307873 | ||||||
chr3:10307972
|
C | G | 9 | a0001c0001t0001g0030a0001c0001t0001g0141a0001c0001t0001g0142others(6): Show | 10 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-2280G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10307972 | ||||||
chr3:10308085
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.451-2393A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308085 | ||||||
chr3:10308219
|
C | G | 1 | a0001c0001t0001g0214 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.451-2527G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308219 | ||||||
chr3:10308480
|
A | AGTC | 3 | a0001c0001t0001g0107a0001c0001t0001g0130a0001c0001t0001g0134 | 3 | HG00642.hp1 HG02451.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.451-2789_451-2788i others(5): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308480 | ||||||
chr3:10308562
|
A | G | 2 | a0001c0001t0001g0173a0001c0001t0005g0211 | 2 | NA18998.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.451-2870T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308562 | ||||||
chr3:10308566
|
T | C | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.451-2874A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308566 | ||||||
chr3:10308653
|
T | C | 3 | a0001c0001t0001g0212a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | HG02055.hp1 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.451-2961A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308653 | ||||||
chr3:10308653
|
TTGAAGAG others(6): Show |
T | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.451-2974_451-2962d others(15): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308653 | ||||||
chr3:10308673
|
C | CTAAT | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0244others(8): Show | 13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-2985_451-2982d others(6): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308673 | ||||||
chr3:10308718
|
ACCC | A | 16 | a0001c0001t0002g0027a0001c0001t0002g0072a0001c0001t0002g0078others(13): Show | 17 | HG01891.hp2 HG02572.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.451-3029_451-3027d others(5): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308718 | ||||||
chr3:10308739
|
A | T | 9 | a0001c0001t0001g0030a0001c0001t0001g0141a0001c0001t0001g0142others(6): Show | 10 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-3047T>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308739 | ||||||
chr3:10308783
|
TGAGTTGA | T | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0244others(8): Show | 13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-3098_451-3092d others(9): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308783 | ||||||
chr3:10308789
|
G | A | 9 | a0001c0001t0001g0030a0001c0001t0001g0141a0001c0001t0001g0142others(6): Show | 10 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-3097C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308789 | ||||||
chr3:10308791
|
A | AT | 10 | a0001c0001t0001g0030a0001c0001t0001g0060a0001c0001t0001g0141others(7): Show | 11 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.451-3100dupA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308791 | ||||||
chr3:10308791
|
AT | A | 92 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(89): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.451-3100delA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308791 | ||||||
chr3:10308791
|
ATT | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(109): Show | 203 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.451-3101_451-3100d others(4): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308791 | ||||||
chr3:10308791
|
ATTT | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 6 | HG01256.hp2 HG02015.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-3102_451-3100d others(5): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308791 | ||||||
chr3:10308792
|
T | A | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0244others(8): Show | 13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.451-3100A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308792 | ||||||
chr3:10308812
|
T | C | 16 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0035others(13): Show | 22 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.451-3120A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308812 | ||||||
chr3:10308814
|
T | A | 6 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(3): Show | 6 | HG00673.hp2 HG01993.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-3122A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308814 | ||||||
chr3:10308865
|
C | T | 4 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0247others(1): Show | 4 | HG00639.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+3100G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308865 | ||||||
chr3:10308933
|
A | AT | 35 | a0001c0001t0001g0043a0001c0001t0001g0212a0001c0001t0001g0217others(32): Show | 40 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.450+3031dupA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308933 | ||||||
chr3:10308933
|
A | ATT | 13 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 18 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.450+3030_450+3031d others(4): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308933 | ||||||
chr3:10308933
|
AT | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(92): Show | 167 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.450+3031delA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308933 | ||||||
chr3:10308933
|
ATT | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(27): Show | 47 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.450+3030_450+3031d others(4): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308933 | ||||||
chr3:10308933
|
ATTTTTTT | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(46): Show | 75 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.450+3025_450+3031d others(9): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10308933 | ||||||
chr3:10309117
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(74): Show | 147 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.450+2848A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309117 | ||||||
chr3:10309126
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.450+2839G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309126 | ||||||
chr3:10309198
|
A | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(75): Show | 148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.450+2767T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309198 | ||||||
chr3:10309284
|
C | CTT | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(75): Show | 148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.450+2679_450+2680d others(4): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309284 | ||||||
chr3:10309490
|
C | T | 1 | a0001c0001t0003g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.450+2475G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309490 | ||||||
chr3:10309497
|
TG | T | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0244others(8): Show | 13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.450+2467delC | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309497 | ||||||
chr3:10309546
|
A | C | 11 | a0001c0001t0001g0030a0001c0001t0001g0141a0001c0001t0001g0142others(8): Show | 12 | HG01070.hp1 HG01071.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.450+2419T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309546 | ||||||
chr3:10309552
|
T | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(85): Show | 160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.450+2413A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309552 | ||||||
chr3:10309590
|
T | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(85): Show | 160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.450+2375A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309590 | ||||||
chr3:10309602
|
A | G | 1 | a0001c0001t0002g0038 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.450+2363T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309602 | ||||||
chr3:10309799
|
A | G | 16 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0035others(13): Show | 22 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.450+2166T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10309799 | ||||||
chr3:10310009
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0200 | 3 | HG01358.hp2 HG01952.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.450+1956C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310009 | ||||||
chr3:10310010
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.450+1955C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310010 | ||||||
chr3:10310039
|
ATCACAGA others(2): Show |
A | 8 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0215others(5): Show | 11 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.450+1917_450+1925d others(11): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310039 | ||||||
chr3:10310146
|
G | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 274 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.450+1819C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310146 | ||||||
chr3:10310245
|
C | T | 1 | a0001c0001t0001g0032 | 2 | HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.450+1720G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310245 | ||||||
chr3:10310264
|
G | C | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.450+1701C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310264 | ||||||
chr3:10310265
|
C | G | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.450+1700G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310265 | ||||||
chr3:10310265
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.450+1700G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310265 | ||||||
chr3:10310348
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.450+1617C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310348 | ||||||
chr3:10310351
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(80): Show | 153 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.450+1614A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310351 | ||||||
chr3:10310423
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.450+1542C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310423 | ||||||
chr3:10310504
|
A | AAAAC | 2 | a0001c0001t0001g0029a0001c0001t0001g0088 | 3 | NA18968.hp1 NA19057.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.450+1457_450+1460d others(6): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310504 | ||||||
chr3:10310559
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0129 | 2 | NA19003.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.450+1406C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310559 | ||||||
chr3:10310581
|
G | A | 1 | a0001c0001t0002g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.450+1384C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310581 | ||||||
chr3:10310669
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.450+1296T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310669 | ||||||
chr3:10310670
|
T | A | 1 | a0001c0001t0001g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.450+1295A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310670 | ||||||
chr3:10310698
|
C | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(74): Show | 147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.450+1267G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310698 | ||||||
chr3:10310796
|
T | C | 16 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0035others(13): Show | 22 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.450+1169A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310796 | ||||||
chr3:10310848
|
A | G | 5 | a0001c0001t0001g0037a0001c0001t0001g0215a0001c0001t0001g0219others(2): Show | 6 | HG01099.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+1117T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310848 | ||||||
chr3:10310886
|
T | G | 1 | a0001c0001t0001g0206 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.450+1079A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310886 | ||||||
chr3:10310904
|
T | G | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.450+1061A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10310904 | ||||||
chr3:10311019
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(74): Show | 147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.450+946G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311019 | ||||||
chr3:10311029
|
TA | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(107): Show | 187 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.450+935delT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311029 | ||||||
chr3:10311059
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.450+906G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311059 | ||||||
chr3:10311081
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+884C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311081 | ||||||
chr3:10311162
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.450+803T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311162 | ||||||
chr3:10311168
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0083others(5): Show | 25 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.450+797G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311168 | ||||||
chr3:10311197
|
G | T | 39 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(36): Show | 56 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.450+768C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311197 | ||||||
chr3:10311327
|
A | C | 1 | a0001c0001t0002g0235 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.450+638T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311327 | ||||||
chr3:10311383
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.450+582C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311383 | ||||||
chr3:10311384
|
C | A | 1 | a0001c0001t0001g0186 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.450+581G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311384 | ||||||
chr3:10311428
|
T | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0162a0001c0001t0001g0187others(2): Show | 9 | HG00408.hp1 HG00673.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.450+537A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311428 | ||||||
chr3:10311458
|
T | G | 27 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0244others(24): Show | 30 | HG00639.hp2 HG01109.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.450+507A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311458 | ||||||
chr3:10311594
|
A | T | 72 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(69): Show | 104 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.450+371T>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311594 | ||||||
chr3:10311646
|
T | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(74): Show | 147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.450+319A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311646 | ||||||
chr3:10311866
|
T | C | 39 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(36): Show | 56 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.450+99A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311866 | ||||||
chr3:10311942
|
C | T | 45 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(42): Show | 62 | HG00099.hp2 HG00673.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.450+23G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 5/8 | chr3 | 10311942 | ||||||
chr3:10312260
|
T | TC | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0213others(1): Show | 6 | HG01884.hp1 HG02145.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-163dupG | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 4/8 | chr3 | 10312260 | ||||||
chr3:10312484
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.316+95G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 4/8 | chr3 | 10312484 | ||||||
chr3:10312517
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0002g0038 | 3 | HG02622.hp1 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.316+62C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 4/8 | chr3 | 10312517 | ||||||
chr3:10312746
|
T | G | 1 | a0001c0001t0001g0189 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.165-16A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10312746 | ||||||
chr3:10312786
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0074 | 2 | HG01192.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.165-56A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10312786 | ||||||
chr3:10312995
|
G | C | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.165-265C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10312995 | ||||||
chr3:10313009
|
C | T | 1 | a0001c0001t0001g0232 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.165-279G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313009 | ||||||
chr3:10313011
|
G | C | 1 | a0001c0001t0001g0212 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.165-281C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313011 | ||||||
chr3:10313087
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.165-357A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313087 | ||||||
chr3:10313156
|
T | C | 26 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0244others(23): Show | 29 | HG00639.hp2 HG01109.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.165-426A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313156 | ||||||
chr3:10313187
|
T | C | 15 | a0001c0001t0002g0027a0001c0001t0002g0078a0001c0001t0002g0081others(12): Show | 16 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.165-457A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313187 | ||||||
chr3:10313290
|
C | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0076 | 3 | HG01070.hp2 HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.165-560G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313290 | ||||||
chr3:10313291
|
G | A | 11 | a0001c0001t0001g0028a0001c0001t0001g0097a0001c0001t0001g0101others(8): Show | 12 | HG02027.hp2 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.165-561C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313291 | ||||||
chr3:10313486
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.165-756A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313486 | ||||||
chr3:10313570
|
C | T | 1 | a0001c0002t0002g0115 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.165-840G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313570 | ||||||
chr3:10313581
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.165-851C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313581 | ||||||
chr3:10313603
|
G | A | 15 | a0001c0001t0002g0027a0001c0001t0002g0078a0001c0001t0002g0081others(12): Show | 16 | HG01891.hp2 HG02572.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.165-873C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313603 | ||||||
chr3:10313641
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.165-911T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313641 | ||||||
chr3:10313791
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0051 | 3 | HG03834.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.165-1061T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313791 | ||||||
chr3:10313841
|
G | C | 1 | a0001c0001t0001g0125 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.165-1111C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313841 | ||||||
chr3:10313900
|
C | G | 48 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(45): Show | 65 | HG00099.hp2 HG00673.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.165-1170G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313900 | ||||||
chr3:10313984
|
C | G | 13 | a0001c0001t0002g0027a0001c0001t0002g0096a0001c0001t0002g0102others(10): Show | 14 | HG01891.hp2 HG02630.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.165-1254G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10313984 | ||||||
chr3:10314100
|
T | G | 1 | a0001c0001t0001g0112 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.164+1221A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314100 | ||||||
chr3:10314122
|
CT | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(73): Show | 147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.164+1198delA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314122 | ||||||
chr3:10314405
|
A | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0141a0001c0001t0001g0142others(8): Show | 12 | HG01070.hp1 HG01071.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.164+916T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314405 | ||||||
chr3:10314462
|
A | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.164+859T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314462 | ||||||
chr3:10314565
|
AT | A | 8 | a0001c0001t0001g0030a0001c0001t0001g0141a0001c0001t0001g0142others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.164+755delA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314565 | ||||||
chr3:10314630
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.164+691G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314630 | ||||||
chr3:10314884
|
T | A | 1 | a0001c0001t0001g0191 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.164+437A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314884 | ||||||
chr3:10314930
|
G | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0068 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.164+391C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10314930 | ||||||
chr3:10315056
|
T | A | 42 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(39): Show | 59 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.164+265A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10315056 | ||||||
chr3:10315076
|
G | A | 56 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(53): Show | 74 | HG00099.hp2 HG00673.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.164+245C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 3/8 | chr3 | 10315076 | ||||||
chr3:10315694
|
C | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0216 | 5 | HG01884.hp1 HG02145.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.49-258G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10315694 | ||||||
chr3:10315701
|
T | G | 1 | a0001c0001t0002g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.49-265A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10315701 | ||||||
chr3:10315709
|
C | T | 5 | a0001c0001t0001g0047a0001c0001t0001g0232a0001c0001t0002g0022others(2): Show | 6 | HG01928.hp1 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-273G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10315709 | ||||||
chr3:10315725
|
G | A | 1 | a0001c0001t0004g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.49-289C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10315725 | ||||||
chr3:10316016
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.49-580G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316016 | ||||||
chr3:10316174
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.49-738G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316174 | ||||||
chr3:10316180
|
G | A | 1 | a0001c0002t0002g0121 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.49-744C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316180 | ||||||
chr3:10316268
|
C | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.49-832G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316268 | ||||||
chr3:10316404
|
A | G | 57 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(54): Show | 85 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.49-968T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316404 | ||||||
chr3:10316412
|
C | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(74): Show | 148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.49-976G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316412 | ||||||
chr3:10316432
|
C | A | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246others(2): Show | 5 | HG00639.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-996G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316432 | ||||||
chr3:10316645
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.49-1209C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316645 | ||||||
chr3:10316740
|
G | A | 67 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(64): Show | 98 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.49-1304C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316740 | ||||||
chr3:10316776
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.48+1274G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316776 | ||||||
chr3:10316853
|
T | C | 58 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(55): Show | 86 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.48+1197A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316853 | ||||||
chr3:10316941
|
C | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(73): Show | 146 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.48+1109G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316941 | ||||||
chr3:10316985
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.48+1065C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10316985 | ||||||
chr3:10317001
|
C | CA | 15 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0037others(12): Show | 21 | HG01099.hp2 HG01106.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.48+1048dupT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317001 | ||||||
chr3:10317001
|
CA | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 140 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.48+1048delT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317001 | ||||||
chr3:10317001
|
CAA | C | 12 | a0001c0001t0001g0066a0001c0001t0001g0087a0001c0001t0001g0097others(9): Show | 12 | HG01071.hp1 HG01175.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.48+1047_48+1048del others(2): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317001 | ||||||
chr3:10317018
|
A | G | 25 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0244others(22): Show | 28 | HG00639.hp2 HG01109.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.48+1032T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317018 | ||||||
chr3:10317038
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(74): Show | 148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.48+1012A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317038 | ||||||
chr3:10317453
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.48+597C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317453 | ||||||
chr3:10317511
|
T | G | 1 | a0001c0001t0001g0139 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.48+539A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317511 | ||||||
chr3:10317566
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(133): Show | 229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.48+484G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317566 | ||||||
chr3:10317654
|
C | T | 1 | a0002c0005t0001g0144 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.48+396G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317654 | ||||||
chr3:10317674
|
C | G | 1 | a0001c0001t0001g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.48+376G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317674 | ||||||
chr3:10317740
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.48+310G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317740 | ||||||
chr3:10317753
|
C | G | 1 | a0001c0001t0001g0017 | 3 | HG00741.hp2 HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.48+297G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317753 | ||||||
chr3:10317778
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.48+272T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317778 | ||||||
chr3:10317779
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.48+271A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317779 | ||||||
chr3:10317944
|
T | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(50): Show | 79 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.48+106A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317944 | ||||||
chr3:10317948
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.48+102A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 2/8 | chr3 | 10317948 | ||||||
chr3:10318145
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.4-51T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318145 | ||||||
chr3:10318184
|
C | CTCAT | 8 | a0001c0001t0001g0030a0001c0001t0001g0141a0001c0001t0001g0142others(5): Show | 9 | HG01070.hp1 HG01071.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.4-94_4-91dupATGA | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318184 | ||||||
chr3:10318188
|
T | C | 26 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0244others(23): Show | 29 | HG00639.hp2 HG01109.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.4-94A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318188 | ||||||
chr3:10318190
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4-96G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318190 | ||||||
chr3:10318325
|
G | A | 47 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(44): Show | 64 | HG00099.hp2 HG00673.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.4-231C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318325 | ||||||
chr3:10318385
|
A | C | 1 | a0001c0001t0001g0008 | 5 | NA18944.hp2 NA18962.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-291T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318385 | ||||||
chr3:10318520
|
C | T | 1 | a0001c0001t0002g0015 | 3 | HG01175.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4-426G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318520 | ||||||
chr3:10318696
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0213others(1): Show | 6 | HG01884.hp1 HG02145.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.4-602C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318696 | ||||||
chr3:10318753
|
T | C | 1 | a0001c0002t0002g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4-659A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318753 | ||||||
chr3:10318970
|
C | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG00673.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.4-876G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10318970 | ||||||
chr3:10319047
|
T | G | 1 | a0001c0001t0001g0199 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.4-953A>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319047 | ||||||
chr3:10319127
|
G | C | 1 | a0001c0001t0001g0073 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4-1033C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319127 | ||||||
chr3:10319241
|
T | C | 6 | a0001c0001t0001g0097a0001c0001t0001g0103a0001c0001t0001g0123others(3): Show | 6 | NA18951.hp1 NA18953.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-1147A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319241 | ||||||
chr3:10319369
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.4-1275A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319369 | ||||||
chr3:10319587
|
G | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG00673.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+1463C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319587 | ||||||
chr3:10319761
|
T | TGA | 3 | a0001c0001t0001g0212a0001c0001t0002g0061a0001c0001t0002g0230 | 3 | HG02559.hp2 HG04115.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3+1287_3+1288dupTC | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319761 | ||||||
chr3:10319761
|
TGA | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0066others(3): Show | 11 | HG02559.hp1 HG02818.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.3+1287_3+1288delTC | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319761 | ||||||
chr3:10319761
|
TGAGA | T | 72 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(69): Show | 101 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.3+1285_3+1288delTC others(2): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319761 | ||||||
chr3:10319761
|
TGAGAGAG others(1): Show |
T | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(69): Show | 143 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.3+1281_3+1288delTC others(6): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319761 | ||||||
chr3:10319761
|
TGAGAGAG others(3): Show |
T | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | NA19085.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.3+1279_3+1288delTC others(8): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319761 | ||||||
chr3:10319761
|
TGAGAGAG others(11): Show |
T | 12 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0046others(9): Show | 14 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.3+1271_3+1288delTC others(16): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319761 | ||||||
chr3:10319777
|
AGAGAGAG others(8): Show |
A | 1 | a0001c0001t0001g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3+1258_3+1272delCT others(13): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319777 | ||||||
chr3:10319790
|
G | A | 1 | a0001c0001t0004g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3+1260C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319790 | ||||||
chr3:10319791
|
A | G | 1 | a0001c0001t0004g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3+1259T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319791 | ||||||
chr3:10319791
|
AG | A | 10 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0001g0068others(7): Show | 11 | HG00735.hp2 HG01891.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3+1258delC | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319791 | ||||||
chr3:10319792
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3+1258C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319792 | ||||||
chr3:10319792
|
G | C | 1 | a0001c0001t0001g0042 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3+1258C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319792 | ||||||
chr3:10319793
|
A | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0004g0062 | 3 | HG00673.hp2 HG02055.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.3+1257T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319793 | ||||||
chr3:10319793
|
A | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0067 | 2 | HG02071.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3+1257T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319793 | ||||||
chr3:10319794
|
GA | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0002g0038others(1): Show | 5 | HG01934.hp2 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+1255delT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319794 | ||||||
chr3:10319795
|
A | C | 1 | a0001c0001t0001g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3+1255T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319795 | ||||||
chr3:10319795
|
A | G | 15 | a0001c0001t0001g0026a0001c0001t0001g0042a0001c0001t0001g0043others(12): Show | 16 | HG00673.hp2 HG00735.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.3+1255T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319795 | ||||||
chr3:10319795
|
AAG | A | 6 | a0001c0001t0001g0030a0001c0001t0001g0146a0001c0001t0001g0218others(3): Show | 7 | HG01070.hp1 HG01071.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+1253_3+1254delCT | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319795 | ||||||
chr3:10319796
|
A | C | 11 | a0001c0001t0001g0026a0001c0001t0001g0045a0001c0001t0001g0068others(8): Show | 12 | HG00735.hp2 HG01891.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+1254T>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319796 | ||||||
chr3:10319796
|
A | G | 11 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0043others(8): Show | 12 | HG00673.hp2 HG01099.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+1254T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319796 | ||||||
chr3:10319797
|
G | A | 6 | a0001c0001t0001g0037a0001c0001t0001g0214a0001c0001t0001g0215others(3): Show | 7 | HG01099.hp2 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+1253C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319797 | ||||||
chr3:10319798
|
G | A | 7 | a0001c0001t0001g0019a0001c0001t0001g0142a0001c0001t0001g0143others(4): Show | 10 | HG00621.hp1 HG01106.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+1252C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319798 | ||||||
chr3:10319799
|
C | A | 13 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0146others(10): Show | 16 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.3+1251G>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319799 | ||||||
chr3:10319799
|
C | G | 22 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0042others(19): Show | 25 | HG00621.hp1 HG00673.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.3+1251G>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319799 | ||||||
chr3:10319799
|
CG | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(87): Show | 161 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.3+1250delC | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319799 | ||||||
chr3:10319799
|
CGGG | C | 37 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0028others(34): Show | 56 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.3+1248_3+1250delCC others(1): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319799 | ||||||
chr3:10319799
|
CGGGG | C | 27 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0036others(24): Show | 34 | HG01081.hp1 HG01255.hp2 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.3+1247_3+1250delCC others(2): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319799 | ||||||
chr3:10319800
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0141a0001c0001t0001g0142others(7): Show | 12 | HG00621.hp1 HG01106.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+1250C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319800 | ||||||
chr3:10319800
|
G | GAGAGAA | 2 | a0001c0001t0001g0037a0001c0001t0001g0219 | 3 | HG01099.hp2 HG02109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3+1249_3+1250insTT others(4): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319800 | ||||||
chr3:10319801
|
G | A | 10 | a0001c0001t0001g0030a0001c0001t0001g0145a0001c0001t0001g0146others(7): Show | 11 | HG00621.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.3+1249C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319801 | ||||||
chr3:10319802
|
G | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0141a0001c0001t0001g0142others(5): Show | 10 | HG01167.hp2 HG01169.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+1248C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319802 | ||||||
chr3:10319802
|
G | C | 1 | a0001c0001t0002g0038 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3+1248C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319802 | ||||||
chr3:10319803
|
G | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0141others(5): Show | 11 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.3+1247C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319803 | ||||||
chr3:10319803
|
G | C | 8 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0214others(5): Show | 9 | HG01099.hp2 HG02109.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.3+1247C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319803 | ||||||
chr3:10319804
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 6 | HG01070.hp1 HG01071.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+1246C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319804 | ||||||
chr3:10319804
|
G | C | 11 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0069others(8): Show | 12 | HG00621.hp1 HG00735.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.3+1246C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319804 | ||||||
chr3:10319804
|
G | T | 1 | a0001c0001t0001g0203 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3+1246C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319804 | ||||||
chr3:10319805
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3+1245C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319805 | ||||||
chr3:10319805
|
G | C | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+1245C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319805 | ||||||
chr3:10319805
|
G | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(71): Show | 145 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.3+1245C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319805 | ||||||
chr3:10319806
|
G | C | 1 | a0001c0001t0001g0019 | 3 | HG01167.hp2 HG01169.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3+1244C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319806 | ||||||
chr3:10319811
|
G | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(72): Show | 146 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.3+1239C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319811 | ||||||
chr3:10319817
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0148 | 2 | HG01993.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.3+1233T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319817 | ||||||
chr3:10319853
|
AGGAG | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG00673.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+1193_3+1196delCT others(2): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319853 | ||||||
chr3:10319864
|
C | CGAGAGAG others(1): Show |
204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 315 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.3+1185_3+1186insTC others(6): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319864 | ||||||
chr3:10319864
|
C | CGGGAGAG others(1): Show |
16 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0026others(13): Show | 22 | HG00735.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.3+1178_3+1185dupTC others(6): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319864 | ||||||
chr3:10319873
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3+1177T>C | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319873 | ||||||
chr3:10319912
|
G | T | 1 | a0001c0001t0002g0225 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3+1138C>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319912 | ||||||
chr3:10319919
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3+1131C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10319919 | ||||||
chr3:10320006
|
G | GGA | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(76): Show | 150 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.3+1042_3+1043dupTC | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320006 | ||||||
chr3:10320006
|
GGAGAGA | G | 40 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0023others(37): Show | 57 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.3+1038_3+1043delTC others(4): Show |
SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320006 | ||||||
chr3:10320032
|
T | A | 1 | a0001c0001t0001g0210 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3+1018A>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320032 | ||||||
chr3:10320269
|
G | C | 1 | a0001c0001t0005g0211 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3+781C>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320269 | ||||||
chr3:10320319
|
T | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0036others(14): Show | 22 | HG00621.hp1 HG01099.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.3+731A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320319 | ||||||
chr3:10320608
|
T | C | 23 | a0001c0001t0001g0232a0001c0001t0001g0243a0001c0001t0002g0020others(20): Show | 28 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.3+442A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320608 | ||||||
chr3:10320685
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3+365A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320685 | ||||||
chr3:10320788
|
T | C | 1 | a0001c0001t0003g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3+262A>G | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320788 | ||||||
chr3:10320865
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG00673.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.3+185G>A | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320865 | ||||||
chr3:10320886
|
G | A | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0244others(8): Show | 13 | HG00639.hp2 HG01109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.3+164C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320886 | ||||||
chr3:10320938
|
G | A | 1 | a0001c0001t0003g0041 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3+112C>T | SEC13 | ENSG00000157020.18 | transcript | ENST00000350697.8 | protein_coding | 1/8 | chr3 | 10320938 |